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Differential
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abdominal cramps
abdominal distention
abdominal muscle paralysis
abdominal protrusion
abducens nerve paralysis
abiotrophy
abortion, spontaneous
abscess, intracerebral
abscess, intracranial
abscess, perivalvular
absence
abulia
acanthocytosis
acanthosis nigricans
aceruloplasminemia
acetazolamide
acetylcholinesterase
acetylcholinesterase deficiency
achilles tendon, enlarged
achondroplasia
acid maltase deficiency
acid maltase deficiency, adult
aciduria
acoustic nerve, vestibular division of
acoustic neurinoma
acoustic neurinoma, bilateral
acquired immunodeficiency syndrome
acral sensory symptoms
acrocyanosis
acromicria
activated protein C resistance
activities of daily living
activities of daily living scale
acute intermittant porphyria
acyl CoA dehydrogenase deficiency
Addison's disease
adducted thumb
adenosine deaminase deficiency
Adies pupil
adolescent medicine
adoption
adrenal mass
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
adrenomyeloneuropathy
adult polyglucosan body disease
adult-onset leukodystrophy, with neuroaxonal spheroids
advances in neurology
adverse drug reaction
adynamia episodica hereditaria
affect, inappropriate
affective disorders
agammaglobulinemia
agenesis of corpus callosum
aggression
agitation
agnosia
agoraphobia
agraphia
Aicardi-Goutieres syndrome
Aicardi's syndrome
airway obstruction
akathisia
akinetic mute
albinism
alcohol
alcohol intolerance
alcohol intoxication
alcohol, blood level of
alcohol, neurologic complications with
alcoholic blackout
alcoholic coma
alcoholic dementia
alcoholic polyneuropathy
alcoholic withdrawal states, DT's, convulsions, etc.
alcoholism
Alexanders disease
Alexanders disease, adult onset
alexia
algorithm
alopecia
alpha galactosidase A deficiency
alpha glucosidase
alpha-fetoprotein
alpha-synuclein
alpha-synuclein gene
Alport syndrome
alternating hemiplegia
alternating hemiplegia of childhood
alternating rapid movement
alternating rapid movement, impaired
alternative medicine
aluminum
alveolar hypoventilation
Alzheimer's disease
Alzheimer's disease, age of onset
Alzheimer's disease, conjugal
Alzheimer's disease, diagnosis of
Alzheimer's disease, early onset
Alzheimer's disease, familial
Alzheimer's disease, familial, late onset
Alzheimer's disease, heterogeneity of
Alzheimer's disease, incidence
Alzheimer's disease, misdiagnosis
Alzheimer's disease, pathogenesis
Alzheimer's disease, preclinical
Alzheimer's disease, risk factors in
Alzheimer's disease, treatment of
Alzheimer's disease, visual variant
amenorrhea
amimia
aminoacidopathies
aminoacidurias
ammonia
amnesia
amniocentesis
amphetamines
amygdala
amyloid
amyloid angiopathy, cerebral
amyloid angiopathy, cerebral, Dutch type
amyloid angiopathy, hereditary cystatin C
amyloid beta protein
amyloid imaging
amyloid plaques
amyloidosis
amyloidosis, oculoleptomeningeal, familial
amyotrophic chorea-acanthocytosis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, atypical
amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, etiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
amyotrophic lateral sclerosis, misdiagnosis
amyotrophic lateral sclerosis, Parkinson-dementia-complex
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, treatment of
ANA
anaplastic large cell lymphoma
anatomy of
anchor bias
anemia
anemia, hemolytic
anesthesia, general
aneuploidy
aneurysm
aneurysm, asymptomatic
aneurysm, berry
aneurysm, intracranial
aneurysm, intracranial, detection
aneurysm, intracranial, familial
aneurysm, intracranial, natural history
aneurysm, intracranial, screening for
aneurysm, intracranial, treatment of
aneurysm, multiple intracranial
aneurysm, ruptured
aneurysm, size
aneurysm, unruptured
Angelman syndrome
angina pectoris
angiofibroma, facial
angiography, cerebral
angiography, posterior fossa
angiography, spinal
angioid streaks
angiokeratoma
angiomyolipomas
anhidrosis
animal exposure
aniridia
ankle edema
ankle reflex, absent
ankle, swelling of
anoctaminopathy
anomic aphasia
anorexia
anorexia nervosa
anosmia
anterior horn cell disease
anterior tibial muscle weakness
anterocollis
anti MAG antibodies
antibiotic prophylaxis
antibiotics
antibiotics, neurologic complications with
antibodies to voltage-gated calcium channels
anticholinergic drugs
anticholinesterase
anticipation
anticoagulant, treatment
anticonvulsants
anticonvulsants, absorption
anticonvulsants, bioavailability
anticonvulsants, blood level determination of
anticonvulsants, compliance
anticonvulsants, discontinuation in seizure-free epileptics
anticonvulsants, effectiveness
anticonvulsants, hypersensitivity syndrome
anticonvulsants, selection of
anticonvulsants, subtherapeutic
anticonvulsants, teratogenicity of
anticonvulsants, untoward effects of
antioxidant
antiphospholipid antibodies
antiphospholipid antibody syndrome
antithrombin III deficiency
antiviral agents
anxiety
aortic valve, bicuspid
aortic valve, insufficiency
aortic valve, lesion of
aortic valve, stenosis
aphasia
aphasia, children
aphasia, progressive
aphasia, progressive, primary
aphasia, transcortical
aphasia, transcortical-sensory
aphonia
apnea
apnea, primary central
apolipoprotein E
APP
APP gene
apraxia
apraxia of eye movements
apraxia, constructional
apraxia, speech
aqueduct of Sylvius, stenosis
aqueduct of Sylvius, stenosis, x-linked
aqueductal stenosis
arachnodactyly
arbovirus
areflexia
arm weakness
Arnold Chiari malformation
aromatic amino acid decarboxylase deficiency
arrhythmia, cardiac
artane
arterial dissection
arterial dissection, aorta
arterial dissection, carotid
arterial dissection, intracranial
arterial dissection, multiple
arterial dissection, precipitating events
arterial dissection, recurrent
arterial dissection, renal artery
arterial dissection, ruptured
arterial dissection, spontaneous
arterial dissection, vertebral
arteriopathy
arteriovenous malformation
arteriovenous malformation, cerebral
arteriovenous malformation, multiple
arteriovenous malformation, pulmonary
arteritis, temporal
arteritis, temporal, conjugal
arthralgia
arthritis
arthrogryposis multiplex
arthropathy
arthropathy, neuropathic
arylsulfatase A
arylsulfatase B
ascites
ash leaf spots
Asians
aspartate aminotransferase
aspartocyclase
Asperger's syndrome
aspiration
aspirin
astrocytoma
astrogliopathy
asymptomatic
asystole
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, congenital
ataxia, hereditary
ataxia, paroxysmal
ataxia, progressive
ataxia, sensory
ataxia, truncal
ataxic gait
ataxin
ataxin-2
atherosclerosis, premature
athetosis
atlanto-axial subluxation
ATP1A3 gene
atrial fibrillation
atrial fibrillation, risk stratification
atrial myxoma
atrial paralysis
atrial septal defect
atrioventricular block
atrioventricular septal defect
attention
attention deficit disorder with hyperactivity
attention span
atypical
audiogram
auditory evoked brainstem potentials
aura
autism
autism, screening for
autistic behavior
autoantibodies
autoimmune basal ganglia encephalitis
autoimmune disease
automatic implantable cardioverter-defibrillator
automobile accidents
autonomic dysfunction
autonomic nervous system
autonomic neuropathy
autonomic neuropathy, idiopathic
autosomal dominant nocturnal frontal lobe epilepsy
autosomal rcessive spastic ataxia of Charlevoix-Saguenay
axonal degeneration
axonal spheroid
azospermia
B 12 deficiency
B12
Babinski sign
baclofen
bacterial endocarditis, neurologic manifestations of
bacterial infection
baldness
Bannayan-Riley-Ruvalcaba syndrome
basal cell carcinoma
basal ganglia
basal ganglia, calcification of
basal ganglia, degeneration
basal ganglia, infarction
basal ganglia, lesion of
basal ganglia, lesion, bilateral
basilar impression
Bassen-Kornzweig syndrome
battered child syndrome
behavior
behavior modification
behavior, combative
behavioral disorder
Behr's optic atrophy
Benedict's solution test
benign essential tremor
benign essential tremor, refractory
benign familial neonatal convulsions
benign sexual headache
bent spine syndrome
benzodiazepine
beta adrenergic blocker
beta-D-glucon
bias
bicaudate index
bifid uvula
bilateral periventricular nodular heterotopia
Binswanger disease
biologic markers
biopterin deficiency
biotin
biotin deficiency
biotin deficiency, juvenile form
biotinidase deficiency
biotin-responsive basal ganglia disease
birth injury
bitemporal visual field defect
blacks
bladder dysfunction
bleeding disorder
blepharospasm
blind spot, enlarged
blindness
blindness, congenital
blindness, sudden
blinking, reduced
blood dyscrasias, neurologic findings with
blood transfusion
blue rubber bleb nevus syndrome
body odor
bone age
bone biopsy
bone density
bone density, increased
bone marrow biopsy
bone marrow transplantation
bone pain
bone scanning
botulinum toxin
botulism
bovine spongiform encephalopathy
boxing
brachial neuritis
brachial neuritis, acute
brachial neuritis, bilateral
brachial plexus
brachial plexus neuropathy
brachial plexus neuropathy, bilateral
brachial plexus neuropathy, familial
brachial plexus neuropathy, recurrent
brachycephaly
bradycardia
bradykinesia
bradyphrenia
BRAF protooncogene
brain atrophy
brain biopsy
brain biopsy, negative
brain biopsy, stereotaxic
brain purpura
brain scan, abnormal
brain transplantation
brainstem
brainstem, atrophy
brainstem, hypoplasia
brainstem, infarction of
brainstem, lesion of
brainstem, malformation
brainstem, neoplasms of
brainstem, vascular malformation of
Brazil
breast feeding
Brown-Vialetto-Van Laere syndrome
Brueghel's syndrome
Brugada syndrome
bruising
bruit
bulbar palsy
bulbar palsy, acute
bulbar palsy, childhood
bulbar palsy, progressive
bulging of biceps
bulimia
buphthalmos
burning feet
burning feet, differential diagnosis of
burning hands
burning paresthesia
burst suppression pattern, electroencephalogram
cachexia
cafe au lait spots
CAG repeats
calcification, gyral
calcification, heart
calcification, intracranial
calcification, intracranial, rim
calcification, muscle
calcifications, intracranial, punctate
calcium antagonist
calcium channel dysfunction
calcium oxalate crystals
calf atrophy
calf hypertrophy
camptocormia
Canavan's disease
cancer of colon
candida albicans
cane
capillary blush
carbamazepine
carbidopa
carbonic anhydrase II deficiency
carcinoembryonic antigen
carcinoma
carcinoma of pancreas
carcinoma of thyroid
carcinoma, multiple
cardiac arrest
cardiac arrest and resuscitation
cardiac surgery
cardiac surgery, hypothermia and circulatory arrest for
cardiac surgery, neurologic complications with
cardiac transplantation
cardiomegaly
cardiomyopathy
caribbean
caries
carnitine deficiency
carnitine deficiency myopathy
carotid artery
carotid artery atherosclerosis
carotid artery disease
carotid artery occlusion, bilateral
carotid artery occlusion, intracranial
carotid artery occlusion, neck
carpal tunnel syndrome
case studies
CAT scan
CAT scan, abdomen
CAT scan, abnormal
CAT scan, abscess, cerebral
CAT scan, angiography
CAT scan, base of skull
CAT scan, chest
CAT scan, contrast enhanced
CAT scan, demyelinating disease
CAT scan, disappearing lesion on
CAT scan, emission
CAT scan, emission, abnormal
CAT scan, false negative
CAT scan, muscle
CAT scan, ring sign
CAT scan, spine
cataplexy
cataracts
cataracts, congenital
catecholamine
caudate nucleus
caudate nucleus, atrophy
caudate nucleus, lesion of
caudate nucleus, lesion of, bilateral
cavernous hemangioma
CD30
Central America
central core disease
central nervous system, infection of
central pontine myelinolysis
cerebellar ataxia, autosomal recessive
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar ataxia, neuropathy and vestibular areflexia syndrome
cerebellar ataxia, primary
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar hemangioma
cerebellar hemorrhage
cerebellar hypoplasia
cerebellar infarction
cerebellar lesion
cerebellar peduncle
cerebellar plaques, amyloid
cerebellar vermis
cerebellum
cerebellum, disease of
cerebellum, neoplasms of
cerebral arteries
cerebral atherosclerosis
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy
cerebral cortex
cerebral cortical atrophy
cerebral edema
cerebral edema, origin and treatment
cerebral edema, vasogenic
cerebral embolism
cerebral embolism, cardiac origin
cerebral embolism, carotid origin
cerebral glucose metabolism
cerebral infarction
cerebral infarction, hemorrhagic
cerebral infarction, small, deep
cerebral infarction, subcortical
cerebral ischemia
cerebral palsy
cerebral palsy, associated problems with
cerebral palsy, etiology
cerebral palsy, pure ataxic
cerebral palsy, risk factors
cerebral palsy, work up
cerebral peduncle
cerebral vasculature
cerebral vasculature, calcification
cerebral venous infarction
cerebral venous thrombosis
cerebral venous thrombosis, etiology
cerebro hepato renal syndrome
cerebroretinal vasculopathy
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, beta-D-glucan
cerebrospinal fluid, biochemical markers of CNS tumors
cerebrospinal fluid, childhood
cerebrospinal fluid, culture of, viral
cerebrospinal fluid, decreased protein of
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, enzymes in
cerebrospinal fluid, gamma amino butyric acid
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, glycine
cerebrospinal fluid, immunoglobulins of
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, pressure increased
cerebrospinal fluid, protein of
cerebrospinal fluid, proteincytologic dissociation
cerebrospinal fluid, red cells in
cerebrospinal fluid, xanthochromia of
cerebrotendinous xanthomatosis
cerebrovascular accident
cerebrovascular accident, bilateral
cerebrovascular accident, cardiac disease causing
cerebrovascular accident, cryptogenic
cerebrovascular accident, etiology
cerebrovascular accident, familial occurrence
cerebrovascular accident, genetic
cerebrovascular accident, infancy and childhood
cerebrovascular accident, intrauterine
cerebrovascular accident, location of
cerebrovascular accident, mimics
cerebrovascular accident, multiple
cerebrovascular accident, neonatal
cerebrovascular accident, non atherosclerotic cause of
cerebrovascular accident, nonvascular territory
cerebrovascular accident, pathophysiology
cerebrovascular accident, prevention of
cerebrovascular accident, recurrent
cerebrovascular accident, silent
cerebrovascular accident, women
cerebrovascular accident, work up for
cerebrovascular accident, young adult
cerebrovascular disease
cerebrovascular disease, cardiovascular disease with
cerebrovascular disease, risk factors in
cerebrovascular disease, surgical treatment of
ceruloplasmin, serum
cesarean section
channelopathy
Charcot-Marie-Tooth
Chediak-Higashi syndrome
chelation therapy
chemotherapy, CNS treatment and complications with
cherry red spot
cherry red spot-myoclonus syndrome
chest x-ray, abnormal
chewing movements
chewing, impaired
chiasmal syndromes
chilbran skin lesions
children
chloride channel dysfunction
choking
cholecystitis
cholelithiasis
cholestanol
cholesterol
cholesterol, HDL
choline acetyltransferase
chondrodysplasia punctata
chorea
chorea, causes of
chorea, familial
chorea, familial benign
chorea, senile
chorea, treatment of
choreoathetosis
choreoathetosis, paroxysmal
choroid plexus
choroid plexus, abnormality of
choroid plexus, cyst
chromosomal abnormality
chromosome 1
chromosome 11
chromosome 12
chromosome 14
chromosome 15
chromosome 16
chromosome 17
chromosome 18
chromosome 19
chromosome 2
chromosome 20
chromosome 20 ring
chromosome 21
chromosome 22
chromosome 3
chromosome 4
chromosome 5
chromosome 6
chromosome 7
chromosome 8
chromosome 9
chronic graft versus host disease
chronic progressive external ophthalmoplegia
cigarette smoking
cingulate gyrus
cingulate island sign
cirrhosis
cirrhosis, causes of childhood
cirrhosis, infancy
cisterna magna, enlarged
cisternogram, radionuclide
cleft lip
cleft palate
clindamycin
Clinical Pathologic Conference(C.P.C.)
clinodactyly
clonazepam
clonidine
clonus
clopidogrel
clubbing of fingers
clubfoot as related to neurologic disease
cluster headache
coagulopathy
coat-hanger pain
Coats syndrome
cobalamin C deficiency
cocaine
Cockayne's syndrome
codfish vertebrae
coenzyme Q10 deficiency
cognition
cognition, slowed
cogwheel rigidty
coin lesion on chest X-ray
cold hands sign
cold intolerance
cold temperature
coldness
collagen vascular disease
collateral circulation
Collier's sign
colloid cyst
coloboma
color vision
color vision, impaired
colpocephaly
coma
coma, episodic
coma, sudden onset
comorbidities
complement deficiency
complete blood count
complicated migraine
complications
compression fracture
compression neuropathy
compression neuropathy, recurrent
compulsivity
conduction block
cone-rod dystrophy
confabulation
confidentiality
confusion
congenital birth defects
congenital deformities
congenital heart disease
congenital heart disease, CNS complications with
congenital infection, viral
congenital malformation
congenital malformation, non CNS
congenital myasthenic syndromes
congenital myopathy
congenital ocular motor apraxia
congestive heart failure
conjunctival biopsy
conjunctivitis
consanguinity
constipation
contractures, joint
contraindications
controversies in neurology
conus medullaris, lesion of
conversion reaction
copper
copper deficiency
copper metabolism, abnormal
coprolalia
cornea
cornea, abnormal
cornea, opacification in infancy-causes of
cornea, opacity of
corneal dystrophy
corneal transplant
Cornelia de Lange syndrome
coronary artery disease
corpus callosum
corpus callosum, atrophy of
corpus callosum, hypoplastic
corpus callosum, infarction of
corpus callosum, lesion of
corpus callosum, thinning
cortical blindness
cortical blindness, transient
cortical vein thrombosis
cost
cost effectiveness
cough
coumarin
counselling
Cowden syndrome
cranial nerve enhancement
cranial nerve enlargement
cranial nerve palsies
cranial nerve palsies, familial
cranial nerve palsies, recurrent
cranial nerve tumor
cranial nerves
cranial neuropathy
cranial neuropathy, multiple
cranio-cervical junction
craniopharyngioma
C-reactive protein, elevated
creatine phosphokinase(CPK)elevated
creatinuria
Cree leukoencephalopathy
Creutzfeldt-Jakob disease, genetic
cricopharyngeal bar
cry, abnormal
cry, weak
crying
crying, pathologic
cryopyrin-associated periodic syndrome
cryptococcal meningitis
cryptorchidism
Cuba
cultured skin fibroblasts
cyanosis
cyclic vomiting
cylindrical spiral
cyst
cyst, peritumoral
cyst, benign intracranial
cyst, bone
cyst, epidermoid of CNS
cyst, neoplastic cerebellum
cyst, odontogenic
cyst, parenchymal
cyst, porencephalic
cyst, ventricular
cystic infarction
cystinosis
cystinuria
cytochrome c oxidase
cytochrome c oxidase, deficiency
cytomegalovirus infection
Danon disease
dantrolene sodium
DARS
D-dimer
deafmute
deafness
deafness, unilateral
decerebrate posture
deep gray nuclei
deep tendon reflexes
deficiency of ADA2
degenerative diseases of CNS
Dejerine-Sottas syndrome
delay in diagnosis
delayed dentition
delayed muscle relaxation
delusion
dementia
dementia, age at onset
dementia, cerebrovascular disease causing
dementia, childhood
dementia, differential diagnosis of
dementia, familial
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
dementia, subcortical
dementia, thalamic
dementia, transmissible
demyelinating disease
denervation of muscle
dental procedure, neurologic complications with
dentate nuclei
dentate nuclei, lesion of
dentatorubral-pallidoluysian atrophy
depression
dermatitis
dermatoglyphics
descending paralysis
desmin
developmental abnormality of brain
developmental disability
developmental evaluation
developmental milestones
developmental milestones, loss of
developmental retardation
developmental venous anomalies
dexterity, impaired
diabetes insipidus
diabetes mellitus
diabetes mellitus, chemical
diabetes mellitus, neurologic manifestations of
diabetes mellitus, ocular complications in
diabetic cranialneuropathies
diagnostic criteria
diaphragmatic paralysis
diarrhea
dichlorphenamide
diet
dieting
differential diagnosis
difficulty climbing stairs
difficulty going down stairs
digital subtraction angiography
digital subtraction angiography, venous
digits, abnormal
dilantin
dilantin, hypersensitivity to
dilantin, toxicity
dilated aortic root
dinitrophenylhydrazine(D.N.P.H.)reaction
diplegia, atonic
diplegia, brachial
diplegia, spastic cerebral
diplopia
diplopia, transient
disability rating scale, neurological
disability, neurological
disconnection syndrome
disinhibition-dementia-parkinsonism-amyotrophic complex
dislocated hip, congenital
disorientation
dissociated sensory loss
distal muscle atrophy
distal muscle weakness
diurnal variation
dizziness
DNA probes
DNA sequencing
donepezil
dopa responsive dystonia
dopamine
dopamine agonist
dopaminergic dysfunction
doppler
double-cortex syndrome
down-beat nystagmus
down-beat nystagmus, primary position of gaze
downward deviation of eyes
Dravet syndrome
drooling
dropped head syndrome
drug abuse
drug induced neurologic disorders
drug interactions
Duane syndrome
duplex ultrasound
dural sinus thrombosis
Durett hemorrhages
dwarfism
dying
dysarthria
dysarthria-clumsy hand syndrome
dyscalculia
dyschromatopsia
dysdiadochokinesia
DYSF gene
dysferlin
dysferlinopathy
dyskinesia, buccal lingual facial
dyslexia
dysmetria
dysmorphic
dysnomia
dysostosis multiplex
dysphagia
dysphasia
dysplasia of C.N.S.
dyspnea
dyspraxia
dyssynergia cerebellaris myoclonica
dystonia
dystonia musculorum deformens
dystonia, cervical
dystonia, children
dystonia, classification
dystonia, etiology of
dystonia, evaluation of
dystonia, face
dystonia, focal
dystonia, painful
dystonia, paroxysmal
dystonia, post traumatic
dystonia, prevalence of
dystonia, symptomatic
dystonia, treatment of
dystonic reaction, acute
dystroglycanopathies
dystrophin
dystrophin associated proteins
DYT1 mutation
ear, abnormal
ear, pain in
early draining vein
ears of the Lynx MR sign
EAST syndrome
eating disorder
echocardiogram
echocardiogram, contrast
echocardiogram, transesophageal, false negative
echocardiogram, transthoracic
echocardiogram, transthoracic, false negative
echolalia
ectatic basilar artery
eczema
edema, facial
edema, pedal
edema, periorbital
efficacy
Ehlers-Danlos syndrome
Ehlers-Danlos syndrome, classification
ejection fraction
ejection fraction, abnormal
electrocardiogram, abnormal
electroconvulsive therapy
electroencephalogram
electroencephalogram, abnormalities of
electroencephalogram, inflammatory disease
electroencephalogram, monitoring, continuous
electroencephalogram, pediatric patients
electroencephalogram, periodic complexes
electroencephalogram, sleep spindles
electroencephalogram, video monitoring with
electromyogram
electromyogram, decremental response
electron microscopy
electronystagmography
electrophoretic pattern, serum
electroretinograph
embolism
embolism, air
embolism, paradoxical
embolism, septic
embolism, systemic
embolization, therapeutic
Embryonal tumors
emergencies, neurologic
emergencies, ocular
Emery-Dreifuss muscular dystrophy
emotional lability
employment
empty sella
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, focal
encephalitis, Rasmussen's
encephalitis, viral
encephalocele
encephalomalacia
encephalopathy
encephalopathy, acute necrotizing
encephalopathy, acute necrotizing of childhood
encephalopathy, anoxic
encephalopathy, metabolic
encephalopathy, neonatal
encephalopathy, progressive
endocarditis
endocarditis, acute bacterial
endocarditis, infectious
endocarditis, prophylaxis
endolymphatic sac tumors
endovascular therapy
enophthalmous
entrapment neuropathy
enzyme treatment
enzyme, defect
enzyme, induction
enzyme, muscle disease
enzyme, serum
ependymoma
ephedrine
epicanthal folds
epidemic
epidemiology of neurology
epidermoid
epileptic encephalopathy
episodic disorders
episodic neurologic deficits
epistaxis
epistaxis, recurrent
epsilon sarcoglycan gene
equinovarus
Erdheim-Chester disease
erectile dysfunction
erythrocyte
erythromelalgia
esophageal varices
ethics in neurology
everolimus
evidence-based research
evoked potentials
excitotoxin
executive dysfunction
exercise
exercise intolerance
exercise-induced neurologic dysfunction
exhibitionism
exome sequencing
exophthalmus
exostosis
extracorporeal membrane oxygenation
extraocular muscle atrophy
extraocular muscle enlargement
extraocular muscle lesion
eye injury
eye movement, disorders of
eye, pain in
eyebrows, abnormal
eyes, sunken
Fabry's disease
face, elongated
face, numbness of
facial anomalies
facial appearance, abnormal
facial expression abnormality
facial hypoplasia
facial nerve palsy
facial nerve palsy, bilateral
facial nerve palsy, familial
facial nerve palsy, recurrent
facial nevus
facial swelling
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
Factor V Leiden
factor V, deficiency
factor VII, deficiency
Fahr disease
failed medical management
failure to thrive
falling
false negative
falx cerebri
familial
familial adult myoclonic epilepsy
familial hemiplegic migraine
familial mediterranean fever
familial periodic ataxia
familial rectal pain
family planning
Farber's disease
FARS2 deficiency
fasciculation
fatal familial insomnia
fatigue
fatty acid dehydrogenase deficiency
fatty acid, elevated plasma content
Fazio-Londe's disease
feeding disorder
ferric chloride test
ferritin, elevated
ferritinemia
fetal alcohol syndrome
fetal tissue
fetus
fever
fibrillations
fibrinolytic agents, contraindications
fibroma, ungual
fibromuscular dysplasia
fine motor function, impaired
finger nose finger test
finger tapping
fingerprint bodies
fingers, abnormal
fish
fistula, arterio-venous
fistula, arterio-venous, carotid-cavernous
fistula, arterio-venous, dural
fistula, arterio-venous, dural, spinal
fistula, arterio-venous, pulmonary
flaccid paralysis
flail arm syndrome
flavivirus
floppy infant
flow study, carotid artery
fluctuate
fluency
flunarizine
fluorescein angiography
fluorescene in situ hybridization
flushing
foam cells
folic acid
foot deformity
foot drop
foot drop, bilateral
fornix, lesion of
fourth ventricle, compression
fourth ventricle, enlargement of
fracture, long bone
fracture, pathologic
Fragile-X associated tremor/ataxia-syndrome
fragile-X syndrome
fragile-X syndrome, carrier
frataxin
free radical
French-Canadian
fried egg appearance
Friedreich's ataxia
Friedreich's ataxia, late onset
frontal balding
frontal bossing
frontal lobe, behavior with disease of
frontal lobe, lesion of
frontal lobe, pathologic signs of
frontotemporal dementia, behavioral variant
fucosidosis
fundus, abnormality of
funduscopic exam
fungal infection
fungal infection, CNS
fusiform gyrus
F-wave response
gabapentin
gadolinium
gait disorder
gait, apraxic
gait, festinating
gait, spastic
gait, waddling
galactocerebrosidase
galactorrhea
galactosemia
galactosidase
gamma amino butyric acid
ganglioglioma
gangliosidosis GM1
gangliosidosis GM2
gangliosidosis, generalized
gargoylism
gastrocnemius muscle weakness
gastrointestinal bleeding
gastrointestinal disease, neurologic complications
gastrointestinal motility
gastrointestinal perforation
gastroparesis
Gaucher's disease
Gaucher's disease, adult onset
gaze palsy
gaze palsy, congenital horizontal
gaze palsy, horizontal
gaze palsy, horizontal-bilateral
gaze palsy, supranuclear
gaze palsy, vertical
gender
gene
gene map
gene mutation
gene therapy
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
genioglossus
genital hypoplasia
genu of corpus callosum
genu valgum
Gerstmann-Straussler-Scheinker disease
gests antagoniste
GFAP gene
giant axonal neuropathy
giant cell reparative granuloma
Gilles de la Tourette syndrome
Gillespie syndrome
Gitelman's syndrome
glabellar sign
glaucoma
glioblastoma multiforme(astrocytoma Gr.III)
glioma
glioma, low-grade
gliomatosis cerebri
gliosis
globoid cells
globus pallidus
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
globus pallidus, stimulation
glucocerebrosidase
glucose level, serum
glucose tolerance test, abnormal
GLUT1
GLUT1 deficiency syndrome
glutamate dehydrogenase deficiency
glutaric acidemia
glutaric aciduria
glycine
glycogen storage disease
glycoprotein
glycosyltransferase
GNAQ gene
gonadal dysgenesis
gonadotropin-releasing hormone
Gorlin-Goltz syndrome
gout
Gowers maneuver
gram positive cocci
granular osmiphilic material
granulomatous disease
grasp reflex
gray hair
gray matter
grimacing
growth hormone
growth hormone deficiency
growth retardation
guanidinoacetate methyltransferase deficiency
Guillain Barre syndrome
Guillain Barre syndrome, familial
gynecomastia
gyrate atrophy of choroid and retina
gyrus, abnormal
hair analysis
hairline, abnormal
Hallervorden Spatz disease
Hallervorden Spatz disease, late onset
Hallgren's syndrome
hallucination
hallucination, auditory
hallucination, hypnagogic
hallucination, visual
haloperidol
hamartin
hamartoma
hammertoes
hand clapping
hand deformity
hand flapping
hand numbness
hand pain
hand weakness
hand wringing
hands, fisted
handwriting
head bobbing
head circumference
head injury
head lag
head nodding
head retraction reflex
headache
headache, awakening with
headache, bifrontal
headache, children
headache, chronic
headache, persistent
headache, positional
headache, progressive
headache, severe
headache, sudden onset of
headache, throbbing
headache, thunderclap
headache, treatment of
headache, unilateral
headache, vascular
headbanging
health insurance
hearing loss
hearing loss, bilateral
hearing loss, congenital
hearing loss, sudden, unilateral
hearing problems in children
heart block
heart block, complete
heart murmur
heart valve surgery
heat intolerance
heavy metal intoxication
heel-knee-shin test
hemangioblastoma
hemangioma
hemangioma, facial
hemangioma, internal organs
hemangioma, leptomeningeal
hemangioma, skin
hematuria, gross
hematuria, microscopic
hemianopia
hemianopia, homonymous
hemianopia, transient
hemidiaphragm, paralysis of
hemidystonia
hemihypertrophy, congenital
hemiparesis
hemiparesis, transient
hemiplegia
hemiplegia, congenital
hemochromatosis
hemochromatosis, primary
hemoglobin abnormality, neurologic complications of
hemolytic-uremic syndrome
hemophagocytic lymphohistiocytosis
hemophagocytic lymphohistiocytosis, cerebromeningeal
hemophagocytosis
hemoptysis
hemorrhage, intracranial, newborn
hemorrhage, periventricular
hemorrhage, putamenal
hemorrhage, thalamic
hemorrhagic diathesis
hemorrhoids
hemosiderosis of CNS, superficial
hepatic encephalopathy
hepatic failure
hepatitis
hepatolenticular degeneration(Wilson's disease)
hepatolenticular degeneration(Wilson's disease), presymptomatic
hepatolenticular degeneration(Wilson's disease), screening for
hepatomegaly
hepatosplenomegaly
heralding manifestation
hereditary hemorrhagic telangiectasia(HHT)
hereditary multiple exostoses
hereditary myopathy with early respiratory failure
herniated disc, lumbar
herniated disc, thoracic
herniation syndromes, intracranial
herpes simplex encephalitis
herpes simplex encephalitis, differential diagnosis of
heterochromia iridis
heterotopia
hexosaminidase-A
hexosaminidase-A and B
HGPPS
hiccoughs
Hicks disease
high arched feet
high arched palate
hip pain
hippocampal atrophy
Hirschprung's disease
hirsutism
Hispanics
histiocytosis
histochemistry
histochemistry of muscle
history of neurology
HLA
hockey stick sign
Hoesch test
holoprosencephaly
Holt-Oram syndrome
homocystinuria
homovanillic acid
hormone replacement
Horner's syndrome
hot cross bun sign
H-reflex testing
HTRA1 gene
human genome
human immunodeficiency virus type 1
human T-lymphotropic virus type I(HTLV-I)
human T-lymphotropic virus type II(HTLV-II)
Hunter's syndrome
huntingtin
Huntington's chorea
Huntington's chorea, differential diagnosis
Huntington's chorea, genetic counselling
Huntington's chorea, late onset
Huntington's chorea, membrane abnormality
Huntington's chorea, misdiagnosis of
Huntington's chorea, presymptomatic detection of
Huntington's chorea, sporadic form
Huntington's disease, children
Hurler's syndrome
hydrocephalus
hydrocephalus, communicating
hydrocephalus, complications with
hydrocephalus, congenital
hydrocephalus, etiology
hydrocephalus, exvacuo
hydrocephalus, fetal
hydrocephalus, intrauterine
hydrocephalus, non-communicating(obstructive)
hydrocephalus, normal pressure
hydrocephalus, normal pressure in children
hydrocephalus, treatment of
hydrocephalus, viral induced
hydronephrosis
hydroxyindole acetic acid 5(5HIAA)
hydroxytryptophan L-5(L-5 HTP)
hydroxyurea
hyperactivity
hyperammonemic encephalopathy
hyperbilirubinemia
hypercalcemia
hypercapnia
hypercholesterolemia
hypercoagulable state
hyperekplexia
hyperglycemia
hyperglycinemia
hyperglycinemia, nonketotic
hyperhidrosis
hyperhomocysteinemia
hyperinsulinism
hyperkalemia
hyperkalemic periodic paralysis
hyperlipidemia
hypernephroma
hyperornithinemia
hyperostosis
hyperostosis corticalis generalisata familiaris
hyperostosis cranialis interna
hyperphagia
hyperpigmentation of skin
hyperpyrexia, CNS disorder causing
hyperreflexia
hypersensitivity reaction
hypersomnia
hypertelorism
hypertension
hyperthermia
hyperthyroidism
hyperthyroidism, familial incidence of
hypertonia
hypertonia, congential
hypertriglyceridemia
hypertrophic cardiomyopathy
hyperuricemia
hypoalbuminemia
hypocalcemia
hypocalcuria
hypocholesterolemia
hypodontia
hypofibrinogenemia
hypogammaglobulinemia
hypoglycemia
hypoglycemic agent, oral
hypoglycemic coma
hypoglycorrhachia
hypogonadism
hypogonadism, hypogonadotropic
hypokalemia
hypokalemic paralysis
hypokalemic periodic paralysis
hypomagnesemia
hypomelanosis of Ito
hypometric saccades
hypomyelination
hyponatremia
hypoparathyroidism
hypophosphatemia
hypopigmentation of skin
hypopituitarism
hyporeflexia
hyposmia
hypotelorism
hypotension, neurologic causes of
hypotension, systemic
hypothalamus, lesion of
hypothermia
hypothyroidism
hypothyroidism, congenital
hypothyroxinemia
hypotonia
hypotonia, infants
hypoxia
hypoxic encephalopathy
hypoxic-ischemic leukoencephalopathy
iatrogenic neurologic disorders
idiopathic polyneuropathy
ileus, paralytic
imbalance
imbalance, postural
immunodeficiency
immunofluorescence
immunohistochemistry
immunologic disease
immunology and the nervous system
immunomodulation
immunoperoxidase staining
immunosuppression
immunosuppressive agents
imperforate anus
implantable cardioverter defibrillator
impotence
impulsivity
in situ hybridization
in vitro fertilisation
inability to sit up
inability to stand on tiptoes
inappropriate behavior
inattention
inborn errors of metabolism
inborn errors of metabolism, screening
incidental finding
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, eosinophilic intranuclear
inclusion bodies, intracytopasmic
inclusion bodies, intranuclear
inclusion bodies, ubiquitin
inclusion body myositis
incontinentia pigmenti
incoordination
infant, evaluation of
infantile bilateral striatal necrosis
infantile hemiplegia
infantile spasm
infection
infection, recurrent
inflexibility, mental
influenza, avian
informed consent
insight, loss
insomnia
insulin resistance
intellectual deficit
intellectual deficit, treatable causes of
intellectual deterioration
intelligence quotient
intelligence testing in children
interferon
interferon alpha
interferon beta 1-a
interferon beta 1-b
interferonopathy
internal capsule
internet
internuclear ophthalmoplegia
interobserver agreement
intestinal biopsy
intestinal pseudoobstruction
intracerebral hemorrhage
intracerebral hemorrhage, familial
intracerebral hemorrhage, lobar
intracerebral hemorrhage, recurrent
intracerebral hemorrhage, small
intracerebral hemorrhage, work up
intracerebral hemorrhage, young adult
intracranial hemorrhage
intracranial hypertension, benign
intracranial hypertension, benign, differential diagnosis
intracranial hypertension, benign, pathogenesis of
intracranial pressure, increased
intranasal medication
intrathecal chemotherapy
intrauterine
intrauterine growth retardation
intrauterine infection
intrauterine infection, viral
intrauterine infection, viral of CNS
intravenous drug abuse
intraventricular hemorrhage
intrinsic hand muscles, wasting of
ipsilateral hemiplegia
iris, abnormal
iritis
iron, brain
iron, serum
iron, serum, low
irritability
ischemic exercise test
islet cell tumor
JAK2 V617F mutation
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
Jakob-Creutzfeldt disease, conjugal
Jakob-Creutzfeldt disease, medical precaution with
Jakob-Creutzfeldt disease, variant
Jakob-Creutzfeldt disease, young adult
Japan
jaundice
jaw closure weakness
jaw contractures
jaw jerk, abnormal
jaw pain
Jervell Lange-Neilson syndrome
Jewish
joint hypermobility
Joubert syndrome
juvenile myoclonus epilepsy
Kallmann's syndrome
karyotyping
Kayser-Fleischer ring
KCNQ2 encephalopathy
Kearns-Sayre syndrome
keratitis
keratoconus
ketamine
ketogenic diet
kinesia paradoxica
Kleine-Levin syndrome
klippel feil syndrome
Kluver-Bucy syndrome
Krabbe's disease
KRIT1 gene
Kugelberg-Welander syndrome
kuru
kyphoscoliosis, neurologic causes of
kyphosis
lactate
lactic acidemia
lactic dehydrogenase(LDH)
lacunar infarction
Lafora body
Lafora's disease
laminopathies
lamotrigine
language delay
language disorder in adults
language disorders in children
laterocollis
laughing, pathologic
Laurence-Moon-Bardet-Biedl syndrome
L-dopa
L-dopa, drug interactions with and side effects of
lead poisoning
learning disability
learning disability, in children
Leber's congenital amaurosis
Leber's hereditary optic neuropathy
leg atrophy
leg spasms
leg spasms, painful
leg weakness, bilateral
leg weakness, unilateral
Legius syndrome
Leigh's disease
Leigh's disease, adult variety
lens, dislocation of
lens, ectopic
lenticonus
lenticular nucleus, lesion of
lenticular nucleus, lesion of, bilateral
leprosy
leptospirosis
Lesch-Nyhan syndrome
lethargy
leucine-rich repeat kinase 2 gene
leukemia
leukemia, neurologic findings assoc.with
leukocyte enzyme abnormality
leukocyte peroxidase
leukocytes
leukocytosis
leukodystrophy
leukodystrophy, 4H
leukodystrophy, pigmented orthochromatic
leukoencephalopathy
leukoencephalopathy with calcification and cysts
leukoencephalopathy, adult onset, sporadic
leukoencephalopathy, differential diagnosis
leukoencephalopathy, hereditary diffuse
leukopenia
level of consciousness, decreased
levonorgestrel
Lewy body
Lewy body disease, diffuse
Lhermitte-Duclos disease
libido, decreased
libido, increased
lid closure, weakness of
lid lag
life expectancy
lifestyle modification
light-near dissociation, causes of
limbic system
limbic-predominant age-related TDP-43 encephalopathy
linear lesion
lip, biting
lipid storage disorder of CNS
lipid storage myopathy
lipomatosis
lipomatosis, multiple symmetrical
lipomembranous polycystic osteodysplasia
Lisch nodules
lissencephaly
livedo reticularis
liver biopsy
liver disease
liver function enzymes
liver transplantation
LMNA gene
lobar atrophy
locus ceruleus, lesion of
long bone lesion
long QT syndrome
long thoracic nerve
lordosis
Lorenzo's oil
loss of sympathy
low back pain
low birth weight
Lowe's syndrome
lumbar canal, stenosis of
lumbar puncture
lumbosacral plexopathy
lumbosacral plexus
lupus anticoagulant
lymphadenopathy
lymphangiomyomatosis
lymphocyte capping, diminished
lymphoma
lymphoma involving CNS
lymphoma, primary of CNS
lysosomal storage disease
lysosomes, abnoral
macrocephaly
macrognathia
macular degeneration
magnetic stimulation, brain
magnetic susceptibility
magnetoencephalography
malabsorption
malaise
malformation, CNS, congenital
malformation, vascular
malformation, vascular, cerebral
malformation, vascular, familial
malformation, vascular, screening for
malformation, Vein of Galen
malignant hyperpyrexia
manganese intoxication
mania
manic-depressive
maple syrup urine disease
marche a petits pas
Marcus Gunn pupil
Marfan syndrome
marfanoid skeletal abnormalities
marihuana
Marinesco-Sjogren syndrome
masked facies
masseter muscle weakness
mastoiditis
McArdle's disease
McLeod syndrome
meconium staining
median neuropathy
medical-legal aspects of neurology
medulla oblongata
medulla oblongata, atrophy
medulla oblongata, lesion of
medulla oblongata, malformation
medulla oblongata, neoplasm of
medulloblastoma
megalencephaly
megalencephaly, idiopathic
melanoma, malignant
melanomatosis, primary malignant
MELAS syndrome
memory, defect of recent
memory, impairment of
meningeal enhancement
meningioma
meningioma, familial
meningioma, multiple
meningismus
meningitis
meningitis, aseptic
meningitis, bacterial
meningitis, basilar
meningitis, candida
meningitis, carcinomatous
meningitis, chronic
meningitis, CSF cell count-normal
meningitis, fungal
meningitis, leptospira
meningitis, meningococcal
meningitis, Mollaret's
meningitis, neutrophilic
meningitis, predisposing factors in
meningitis, recurrent
meningitis, relapse
meningocele
meningoencephalitis
menses
mental retardation
mental retardation, etiology of
mental retardation, familial
mental status, abnormal
meralgia paresthetica
merlin
merosin
MERRF syndrome
mesial temporal lobe
mesial temporal lobe epilepsy
mesial temporal sclerosis
mestinon
metabolic acidosis
metabolic alkalosis
metabolic disorder, primary
metabolic disorder, primary-screening tests
metachromatic leukodystrophy
metachromatic leukodystrophy, adult onset
metachromatic leukodystrophy, juvenile
methylene tetrahydrofolate reductase
methylenetetrahydrofolate reductase deficiency
methylmalonic acidemia
methylmalonic aciduria
metoprolol
metronidazole
Mexican
Mexico
mexiletine
microangiopathic hemolytic anemia
microangiopathy, brain
microcephaly
microdontia
micrognathia
micrographia
microhemorrhage, intracerebral
micromelia
micropolygyria
microspherophakia
microsurgery
midbrain, atrophy
midbrain, lesion of
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
middle cerebral artery territory infarction
middle cerebral artery, occlusion of
midline defect in children
migraine
migraine with aura
migraine, aura of
migraine, children
migraine, confusional state and delirium with
migraine, EEG in
migraine, hemiplegic
migraine, mental disorder associated with
migraine, pathogenesis
migraine, treatment of
migraine, triggers
migraine, without headache
mild cognitive impairment
Miller-Dieker syndrome
Mills syndrome
mimics
Minamata disease
Mini Mental Status Examination
misdiagnosis
mitochondrial disease
mitochondrial disease, pathogenesis
mitochondrial encephalomyopathy
mitral valve lesion
mitral valve prolapse
MNGIE syndrome
molecular genetics
molecular markers
molybdenum cofactor deficiency
mongolism
monoclonal antibodies
monomelic amyotrophy
mononeuropathy
mononeuropathy multiplex
mononeuropathy, children
mononeuropathy, recurrent
monoparesis
mood change
Morquio syndrome
mortality
mosquito
motor cortex
motor dysfunction
motor neuron disease
motor signs
mousy odor
movement disorder
movement disorder, drug induced
movement disorder, extrapyramidal
movement disorder, paroxysmal
movement disorder, treatment of
moyamoya
moyamoya, adult
MRI
MRI pattern
MRI, abdomen
MRI, abnormal
MRI, angiography
MRI, black holes on
MRI, brachial plexus
MRI, CAT scan compared to
MRI, complications with
MRI, contrast enhanced
MRI, cranial nerves
MRI, diffusion tensor
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, eye of tiger sign
MRI, false negative
MRI, fetal
MRI, FLAIR
MRI, functional
MRI, gradient-echo
MRI, high signal foci on
MRI, high signal intensity of basal ganglia
MRI, hypointense signal foci on
MRI, incidental finding
MRI, indications for
MRI, mass effect on
MRI, muscle
MRI, negative
MRI, nodular enhancement
MRI, optic nerve
MRI, paramagnetic effect
MRI, perfusion
MRI, peripheral nerve
MRI, punctate pattern
MRI, ring sign
MRI, serial
MRI, spinal cord
MRI, spinal cord, increased intramedullary cord signal
MRI, spine
MRI, susceptibility weighted
MRI, T1 weighted high signal foci
MRI, target sign
MRI, venography
MRI, volumetry
MRS
mucopolysaccharidoses
mucopolysacchariduria
multicore myopathy
multiminicore disease
multiple endocrine neoplasia
multiple sclerosis
multiple sclerosis, asymptomatic
multiple sclerosis, clinical patterns
multiple sclerosis, conjugal
multiple sclerosis, diagnosis of
multiple sclerosis, differential diagnosis of
multiple sclerosis, etiology of
multiple sclerosis, familial
multiple sclerosis, linoleic acid in
multiple sclerosis, misdiagnosis
multiple sclerosis, parental transmission
multiple sclerosis, pathogenesis
multiple sclerosis, risk factors for
multiple sclerosis, treatment of
multiple system atrophy
muscle atrophy, focal
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle cramp
muscle culture
muscle diseases, characteristics of
muscle hypertrophy
muscle pain
muscle phosphorylase deficiency
muscle spasm
muscle stiffness
muscle swelling
muscle tenderness
muscle twitching
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscle weakness, sudden onset of
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, Becker, carrier
muscular dystrophy, cardiovascular changes with
muscular dystrophy, central nervous system abnormality
muscular dystrophy, classification
muscular dystrophy, congenital
muscular dystrophy, congenital, Fukuyama type
muscular dystrophy, differential diagnosis of
muscular dystrophy, distal, Miyoshi
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, Duchenne, neonatal screening
muscular dystrophy, Duchenne, presymptomatic detection
muscular dystrophy, dystrophin normal
muscular dystrophy, facioscapulohumeral
muscular dystrophy, female occurrence of
muscular dystrophy, limb-girdle
muscular dystrophy, lymphocyte capping, diminished
muscular dystrophy, neurogenic hypothesis of
muscular dystrophy, systemic membrane defect
mutism
myasthenia gravis
myasthenia gravis, congenital
myasthenia gravis, differential diagnosis
myasthenia gravis, distal weakness
myasthenia gravis, etiology of
myasthenia gravis, familial incidence of
myasthenia gravis, infantile and juvenile
myasthenia gravis, limb-girdle
myasthenia gravis, misdiagnosis of
myasthenia gravis, neonatal
myasthenia gravis, neuromuscular junction in
myasthenia gravis, nystagmus in
myasthenia gravis, ocular
myasthenia gravis, receptor site in
myasthenia gravis, sensory loss with
myasthenia gravis, seronegative
myasthenia gravis, treatment of
myasthenic syndrome
myelin basic protein gene
myelin protein zero gene
myelination of nervous system
myelitis
myelitis, longitudinal
myelitis, transverse
myelodysplasia
myelogram
myelomalacia
myelomeningocele
myeloneuropathy
myelopathy
myelopathy, chronic progressive
myeloproliferative disorder
myoblast transfer
myocardial abscess
myocardial biopsy
myocardial infarction
myocardial injury
myoclonic dystonia
myoclonic jerks
myoclonus
myoclonus, action
myoclonus, cortical
myoclonus, epilepsy
myoclonus, essential
myoclonus, sleep
myoclonus, stimulus sensitive
myocytolysis
myoedema
myoglobinuria
myokymia
myopathy
myopathy, alcoholic
myopathy, centronuclear
myopathy, desmin
myopathy, distal
myopathy, distal Laing
myopathy, distal, vacuolar
myopathy, distal, Welander's
myopathy, drug-induced
myopathy, genetic
myopathy, hereditary
myopathy, inclusion body
myopathy, inclusion body with Paget's disease
myopathy, inclusion body, hereditary
myopathy, metabolic
myopathy, mitochondrial
myopathy, myofibrillar
myopathy, necrotizing
myopathy, proximal
myopathy, quadriceps
myopathy, vacuolar
myopia
myositis, ocular
myostatin
myotonia
myotonia congenita
myotonia dystrophica
myotonia dystrophica, classification
myotonia dystrophica, type 2
myotonia, causes of
myotonic discharges
mysoline
N-acetylcysteine
narcolepsy
nasal bridge, wide
nasal speech
nasal stuffiness
Native Americans
nausea and vomiting
neck pain
neck weakness
neck, webbed
needle tracks
negative
nemaline rod myopathy
nemaline rod myopathy, adult onset
neonatal epilepsy syndromes
neonatal epileptic encephalopathy
neonatal screening, genetic neurologic disorders
neoplasm, intracranial
neoplasm, intracranial, multiple
neoplasm, intracranial-incidence and epidemiology of
neoplasm, metastatic to CNS
neoplasm, metastatic to CNS-treatment of
neoplasm, peripheral nerve
neoplasm, posterior fossa
neoplasm, primary intracerebral
neoplasm, primary intracerebral, reoperation
neoplasm, primary intracranial
neoplasm, primary intracranial-treatment of
neoplasm, primary of CNS
neoplasm, primary of CNS assoc.with primary malig.other sites
neoplasm, primary of CNS-aged
neoplasm, primary of CNS-children
neoplasm, primary of CNS-classification
neoplasm, primary of CNS-familial occurrence
neoplasm, primary of CNS-incidence of
neoplasm, primary of CNS-multiple
neoplasm, primary of CNS-recurrent
neoplasm, primary of CNS-surgical treatment of
neoplasm, primary of CNS-survival
neoplasm, primary of CNS-treatment of
nephritis
nephrocalcinosis
nephrotic syndrome
nerve biopsy
nerve conduction studies
nerve conduction studies, motor
nerve conduction studies, sensory
nerve culture
nerve growth factor
nerve hypertrophy
nerve root enhancement
nerve root hypertrophy
neural tube defect
neuraminidase deficiency
neuritis
neuroaxonal dystrophy
neuroaxonal dystrophy, infantile
neuroaxonal dystrophy, juvenile
neuroaxonal leukodystrophy
neuroblastoma
neurocardiology
neurochemistry
neurocutaneous disease
neurodegeneration with brain iron accumulation
neuroendocrinology
neurofibrillary degeneration
neurofibroma
neurofibromatosis 1
neurofibromatosis 2
neurofibromatosis 2, presymptomatic
neurofibromin
neurogenic bladder
neurogenic vs.myopathic atrophy
neuroichthyosis
neuroleptic
neurolipidosis IV
neurologic complications of, chronic pulmonary disease
neurologic complications of, surgery
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic disease, tempo
neurologic evaluation
neurologic examination
neurologic examination, focal
neurologic history
neurologic practice
neurologic signs
neurologic symptoms
neurologic testing
neuroma
neuromuscular blockade
neuromuscular disease, electrodiagnosis of
neuromuscular junction
neuromuscular junction, abnormality of
neuromyelitis optica (Devic's disease)
neuromyelitis optica spectrum disorder
neuromyelitis optica, IgG
neuromyotonia
neuromyotonia and axonal neuropathy
neuronal ceroid-lipofuscinosis
neuronal degeneration
neuronal intranuclear inclusion disease
neuronal migration disorder
neuronopathy
neuronopathy, sensory
neurons
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
neuropathy, amyloid
neuropathy, ataxia, retinitis pigmentosa
neuropathy, ataxic
neuropathy, classification of
neuropathy, demyelinating
neuropathy, diabetic
neuropathy, etiologies of
neuropathy, hereditary peripheral
neuropathy, hypertrophic
neuropathy, iatrogenic
neuropathy, motor
neuropathy, onion bulb
neuropathy, painful
neuropathy, peripheral
neuropathy, peripheral, treatment
neuropathy, sensory
neuropathy, sensory, hereditary
neuropathy, toxic
neuropathy, work up for
neuropsychiatry
neurosis
neurotomy
neurotoxic
neurotoxin
neurotransmitter
neutropenia
nevoid basal cell carcinoma syndrome
nevus
newborn, evaluation of
next-generation sequencing
NF1 gene
Niemann-Pick disease
night blindness
nigrostriatal pathway
NMDA antagonists
NMDA receptors
Noonan Syndrome
normal
Norrie Disease
nose, abnormal
NOTCH2NLC
Notch3 gene
Notch3 gene, false negative
numbness, extremity
nusinersen
nutritional deficiency
nystagmus
nystagmus, dissociated
nystagmus, gaze-evoked
nystagmus, gaze-paretic
nystagmus, hereditary
nystagmus, monocular
nystagmus, pendular
nystagmus, periodic
nystagmus, primary position of gaze
nystagmus, rotary
nystagmus, upbeating-in primary position of gaze
nystagmus, vertical
obesity
obsessive-compulsive disorder
obstetric neurologic injuries
occipital lobe
occipital lobe, infarction
occipital lobe, lesion of
occupational neurologic disorders
ocular motility, disorders of
ocular myopathy
oculodentodigital dysplasia
oculogyric crisis
oculopharyngeal muscular dystrophy
old age, neurology of
olfactory bulb
oligodactyly
oligodendroglioma
omeprazole
omphalocele
Ondine's curse
opened mouth
operculum syndrome
operculum syndrome, bilateral
ophthalmic artery occlusion
ophthalmoplegia
ophthalmoplegia, progressive external
opiate
opisthotonus
optic atrophy
optic atrophy, bilateral
optic atrophy, hereditary
optic chiasm
optic chiasm, enlarged
optic disc cup
optic disc edema
optic foramina
optic foramina, abnormal
optic glioma
optic nerve
optic nerve sheath fenestration
optic nerve, compression of
optic nerve, decompression of
optic nerve, enhancement
optic nerve, enlarged
optic nerve, hypoplasia of
optic nerve, lesion of
optic nerve, neoplasm of
optic neuritis
optic neuritis, bilateral
optic neuropathy
optic neuropathy, bilateral
optic neuropathy, hereditary
optical coherence tomography
optokinetic nystagmus, abnormal
oral contraceptives
orbit
orbit, lesions of
orbit, tomograms of
organ rupture
orgasm
ornithine transcarbamylase deficiency
orthopnea
orthostatic hypotension
oscillopsia
osteogenesis imperfecta
osteopetrosis
osteoporosis
osteosclerosis, autosomal dominant
otitis, neurologic complications with
otosclerosis
overlap syndrome
owl's eye sign of spinal cord
oxalosis, primary
oxazepam
pacemaker, cardiac-transvenous
pachygyria
Paget's disease
Paget's disease, spinal cord problem in
pain
pain, abdominal
pain, anal
pain, arm
pain, back
pain, flank
pain, foot
pain, head
pain, increased response
pain, leg
pain, periorbital
pain, severe
pain, wrist
palatal myoclonus
palatopharyngeal incompetence
palilalia
palliative care
pallido-ponto-nigral degeneration
pallidotomy
Pallister-Hall syndrome
palmoplantar keratoderma
palpitations
pancreatic cyst
pancreatitis
pancytopenia
panic attacks
PANK2 mutation
papilledema
paralysis
paralysis, acute
paralysis, acute areflexic
paralysis, asymmetric
paralysis, recurrent
paramyotonia congenita
paranoia
paraoxonase
paraparesis
paraparesis, acute
paraparesis, familial spastic
paraparesis, familial spastic, classification
paraparesis, familial spastic, variants
paraparesis, spastic
paraparesis, spastic, tropical
paraparesis, transient
paraplegia
paraplegia, recurrent
paraplegin
paraspinal muscle
paraspinal muscle weakness
paratonia
paresthesias
paresthesias, feet
paresthesias, lower extremity
PARK genes
parkin gene
Parkinson disease
Parkinson disease, arteriosclerotic
Parkinson disease, atypical
Parkinson disease, benign tremulous
Parkinson disease, classification
Parkinson disease, dementia with
Parkinson disease, diagnosis
Parkinson disease, differential diagnosis of
Parkinson disease, dystonia with
Parkinson disease, early symptoms
Parkinson disease, etiology of
Parkinson disease, familial
Parkinson disease, fluctuations in
Parkinson disease, freezing phenomena in
Parkinson disease, heterogeneity of
Parkinson disease, juvenile
Parkinson disease, L-dopa nonresponsive
Parkinson disease, nonmotor problems of
Parkinson disease, pathogenesis of
Parkinson disease, presymptomatic detection
Parkinson disease, rapid onset
Parkinson disease, rapid progression
Parkinson disease, subtypes
Parkinson disease, surgical treatment of
Parkinson disease, treatment of
Parkinson disease, young onset
Parkinsonism multiple-system atrophy
Parkinsonism plus syndrome
Parkinsonism syndrome
Parkinsonism-dementia complex
paroxysmal dystonic choreoathetosis
paroxysmal exercise-induced dyskinesia
paroxysmal exertion-induced dyskinesia
paroxysmal extreme pain disorder
paroxysmal hypnogenic dyskinesia
paroxysmal kinesigenic dyskinesia
paroxysmal neurologic deficits
paroxysmal neurologic disorder
PAS positive
PAS positive material in the brain
past pointing
patent foramen ovale
pathognomonic
pathologic reflex
pathology
patient in waiting
patient information and support
pectus carinatum
pectus excavatum
pediatric neurology
Pelizaeus Merzbacher
penicillamine
penis, pigmented macules
peptides, brain
percussion induced muscle contraction
periodic limb movements
periodic movements during sleep
periodic paralysis
periodic paralysis, thyrotoxic
peripheral blood smear
peripheral nerve, lesion of
periventricular leukomalacia
peroneal muscle atrophy, causes of
peroneal nerve
peroneal nerve palsy
peroneal nerve, lesion of
peroxisomal disease
peroxisomes
perseveration
personality change
pes cavus
phakomatoses
phenobarbital
phenylketonuria
phenylketonuria, adult onset
pheochromocytoma
phlebotomy
phocomelia
phonophobia
phosphorylase b kinase deficiency
photic sneeze reflex
photophobia
photosensitivity, skin
phytanic acid
Pick bodies
Pick's disease
pigmentary retinopathy
pigmented macules
pimozide
pineal, neoplasm
pineoblastoma
Pittsburgh Compound B
pituitary, adenoma
pituitary, hormones of
placebo effect
platelet aggregation
platelet inhibiting drugs
pleocytosis of cerebrospinal fluid
pleocytosis of cerebrospinal fluid, neutrophilic
pleural effusion
pneumonia
pneumothorax
poison, mercury
poison, neurologic problems with
POLG1 gene
POLR3B
polycystic kidneys
polycystic lipomembranous osteodysplasia
polycythemia, primary
polycythemia, secondary
polydactyly
polyglucosan body
polyglucosan body disease
polyhydramnios
polymerase chain reaction
polymerase chain reaction, false negative
polymerase chain reaction, false positive
polymicrogyria
polymyositis
polyneuropathy
polyneuropathy, chronic idiopathic
polyneuropathy, chronic inflammatory demyelinating
polyneuropathy, chronic relapsing
polyneuropathy, familial
polyps, gastrointestinal tract
Pompe's disease of glycogen storage
pons, atrophy
pons, hypoplasia
pons, lesion of
pontocerebellar atrophy
porphyria
port wine nevus
portal caval shunt
positional head-hanging test
positive sharp waves
post hemorrhagic hydrocephalus
posterior cerebral artery territory infarction
posterior column disease
posterior cortical atrophy
posterior fossa, lesion of
posterior leukoencephalopathy syndrome
postoperative neurologic complications
postpartum
postpartum coma
postural abnormality
potassium
potassium channel antibodies
potassium channel dysfunction
practice guidelines
Prader-Labhart-Willi syndrome
pramipexole
precipitating factors
preclinical
precocious puberty
pregnancy, anticonvulsants during
pregnancy, neurologic complications in
premature infant
premature infant, problems in
prenatal
prenatal diagnosis by amniocentesis
presenilin-1 gene
presenilin-2 gene
pretectal syndrome
prethrombotic state
prevention of neurologic disorders
primary episodic ataxia
primary lateral sclerosis
primary thrombocythemia
prion disease
prion protein gene
procyclidine
progeria
prognathism
prognosis
progressive infantile poliodystrophy
progressive multifocal leucoencephalopathy
progressive myoclonic epilepsy
progressive neurologic disorder
progressive pallidum atrophy
progressive spinal muscular atrophy
progressive subcortical gliosis
prolactin, elevated
propionic aciduria
propranolol
proprioception, abnormal
prostigmine
protein 14-3-3, cerebrospinal fluid
protein C deficiency
protein S deficiency
proteinopathy
proteinuria
proton pump inhibitors
proximal muscle atrophy
proximal myotonic myopathy
pruritus
pseudarthrosis
pseudobulbar palsy
pseudohypertrophy
pseudointernuclear ophthalmoplegia
pseudomyasthenia
pseudomyotonia
pseudoretinitis pigmentosa
pseudotumor
pseudoxanthoma elasticum
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychological testing, children
psychological testing, neurologic problems
psychomotor retardation
psychosis
psychosis, acute
psychosis, childhood
psychosocial aspects
psychotic behavior
ptosis
ptosis, bilateral
ptosis, familial
ptosis, unilateral
puerperium
Puerto Rico
pull test
pulmonary disease
pulmonary embolism
pulmonary hypertension
pulmonary infiltrates
pulmonary stenosis
pulvinar sign
pupil
pupil, abnormality in neurologic disorders
pupil, dilated and fixed, bilateral
pupil, dilated, bilateral
pupil, dilated, episodic
pupil, ectopic-congenital
pupil, light reflex, abnormal
Purkinje cell
pursuit eye movements, abnormal
putamen, lesion of
putamen, lesion of, bilateral
pyramidal
pyramidal tract
pyramidal tract dysfunction
pyramidal tract, uncrossed
pyridoxine
pyridoxine deficiency
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
quadriceps atrophy
quadriceps weakness
quadriparesis
quadriparesis, acute
quadriplegia
quadriplegia, transient
quality of life
radial nerve, palsy of
radiation hypersensitivity
radiation therapy, CNS treatment and complications with
radiation therapy, stereotactic
radiculopathy
ragged-red fibers
Rankin score
raphe nuclei
rapid onset dystonia parkinsonism
rapidly fatal neurologic illness
rapidly progressing neurologic illness
rash
reaction time
reading disorder, acquired
reading problem, causes of
real-time quaking-induced conversion
recombinant DNA
recruitment
recruitment, reduced
rectal biopsy
recurrent
Red flags
reduplicative paramnesia
refractive errors
Refsum's disease
regional enteritis
release phenomena
REM sleep
remote effect of cancer on the nervous system
renal biopsy
renal cell carcinoma
renal cyst
renal dysplasia
renal failure
renal failure, acute
renal infarct
renal stones
renal transplantation
renal tubular acidosis
repetitive nerve stimulation
research
respirations in CNS disease
respirator
respiratory depression
respiratory failure
respiratory tract infection
restless leg syndrome
retina, abnormal
retinal artery tortuosity
retinal degeneration
retinal detachment
retinal dysplasia
retinal hamartoma
retinal hemangioma
retinal hemorrhages
retinal ischemia
retinal lesion
retinal microvascular disease
retinal tumor
retinal vasculitis
retinal vasculopathy
retinal vasculopathy with cerebral leukodystrophy
retinitis pigmentosa
retinoblastoma
retinopathy
retrocollis
retroperitoneal mass
retropulsion
Rett's syndrome
reversible neurologic disorder
review article
RFLPs
rhabdomyolysis
rhabdomyoma, cardiac
rhabdomyosarcoma of heart
rheumatoid arthritis
rheumatoid arthritis, neurologic complications of
rhizomelia
riboflavin
riboflavin transporter deficiency
rickets
Rieger's anomaly
rigid spine syndrome
rigidity
Riley-Day syndrome
riluzole
rippling muscle disease
risk factors
risk factors, modification
risk-benefit assessment
risus sardonicus
ritalin
rituximab
Romano-Ward syndrome
Romberg's sign
root lesion, nerve
Rosenthal fibers
Roussy Levy syndrome
rubella syndrome
running
saccadic eye movements
saccadic eye movements, abnormal
saddle nose
safety
salivation, excessive
Sandhoff's disease
Sanfilippo syndrome
sarcoglycan
sarcoidosis
sarcoidosis, CNS
sarpropterin
Saudi Arabia
Schilder's disease
schizophrenia
schwannoma
sclerae, blue
sclerosis, bone
sclerosteosis
SCN1A gene
scoliosis
scoliosis, neurologic association with
scotoma
scotoma, central
scrapie
screaming
screening
sea-blue histiocytes
second wind phenomena
sedimentation rate, elevated
seizure
seizure, advice to parents and teachers regarding
seizure, bathing induced
seizure, cardiac arrhythmia causing
seizure, children
seizure, classification of
seizure, complications following
seizure, diagnosis of
seizure, differential diagnosis of
seizure, drug resistance
seizure, drug-induced
seizure, etiology of
seizure, familial
seizure, febrile
seizure, focal
seizure, hereditary
seizure, incidence of
seizure, injury following
seizure, intractable
seizure, intractable, treatment of
seizure, maternal
seizure, neonatal
seizure, nocturnal
seizure, nonepileptic
seizure, paradoxical
seizure, photosensitive
seizure, precipitating factors
seizure, pregnancy
seizure, prevalence of
seizure, prognosis in adults
seizure, prognosis in childhood
seizure, psychomotor-temporal lobe
seizure, psychosocial aspects of
seizure, pyridoxine dependent
seizure, risk factors for
seizure, stimulus sensitive
seizure, surgical treatment of
seizure, teenager
seizure, tonic-clonic
seizure, treatment of
seizure, treatment of, monotherapy
seizure, women
seizure, workup of
self-mutilation
sella turcica, enlargement of
semialdehyde dehydrogenase deficiency
senile plaques
sensorineural hearing loss
sensory ganglia
sensory ganglia, abnormal
sensory loss
sensory loss, truncal
sensory nerve action potentials
sensory polyneuropathy
sensory tricks
serologic testing
seronegative
serotonin
serratus anterior muscle, weakness
sexual behavior, disorder of
sexual intercourse
shagreen patch
shaking
short neck
short stature
shoulder, numbness
shoulder, pain in
shoulder-girdle wasting
shunt procedure, lumboperitoneal
shunt procedure, ventricular
shunt procedure, ventricular-complications of
shunt procedure, ventriculo-amniotic
Shy-Drager syndrome
sibling
sick sinus syndrome
sickle cell disease
simian crease
simultanagnosia
sinemet
single photon emission computed tomography
Sjogren-Larsson syndrome
skin, biopsy
skin, darkening of
skin, hyperextensible
skin, lesions in neurologic disorders
skin, thin
skin, translucent
skull x-ray, abnormal
skull x-ray, bony defect on
sleep
sleep apnea
sleep apnea, obstructive
sleep paralysis
sleep pathology and physiology
slit lamp examination
sloped shoulders
slow virus infection of CNS
slurred speech
small vessel disease
smell
Smell Identification Test
smiling
SMN1 gene
SNCA duplication
Sneddon's syndrome
sneeze
snoring
snout reflex
socialisation
sodium channel dysfunction
sodium valproate
somatosensory evoked potentials
somatostatin
somnolence
sore throat
South America
Southern immunoblot test
spartin
spastic ataxia
spastic diplegia
spastic dysphonia
spastic paraplegia, type 11
spastic paraplegia, type 15
spastic paraplegia, type 7
spasticity
spastin
speech disorder
speech disorder, childhood
speech disorder, non aphasic
speech, delayed development of
speech, loss of
speech, slowed
speech, soft
sphingolipodoses
sphingomyelin
Spielmeyer Vogt syndrome
spina bifida
spinal cord
spinal cord degeneration
spinal cord, compression of
spinal cord, extramedullary cyst of
spinal cord, infarction of
spinal cord, lesion of
spinal cord, neoplasm
spinal cord, neoplasm, extramedullary
spinal cord, neoplasm, extramedullary intradural
spinal cord, neoplasm, intramedullary
spinal cord, neoplasm, neurofibroma
spinal cord, pathologic exam of
spinal cord, vascular disorders Affecting
spinal cord, vascular malformation of
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, classification
spinal muscular atrophy, intermediate form
spinal stenosis
spinal stenosis, familial
spinal xanthomatosis
spine, metastasis to
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 10
spinocerebellar ataxia type 12
spinocerebellar ataxia type 14
spinocerebellar ataxia type 16
spinocerebellar ataxia type 17
spinocerebellar ataxia type 2
spinocerebellar ataxia type 3/Machado Joseph disease
spinocerebellar ataxia type 5
spinocerebellar ataxia type 6
spinocerebellar ataxia type 7
spinocerebellar ataxia type 8
spinocerebellar degeneration
spinopontine atrophy, dominant
spirochete infection
splenium of corpus callosum
splenomegaly
spondylolisthesis
spondylolysis
spondylosis
spongy degeneration of brain
spontaneous muscle activity
spontaneous remission
sports medicine, neurology of
spreading cortical depression
SPRED1 mutation
squirrels
staggering
standing difficulty
staphylococcus aureus
stare
startle myoclonus
startle reaction
status epilepticus
steatorrhea
stem cell transplantation
stent, venous sinus
steppage gait
stereotaxic surgery
stereotyped behavior
stereotyped behavior, drug induced
stereotypy
steroid
steroid therapy, CNS treatment and complications with
stimulant drugs
stimulation, deep brain
stooped posture
storage disease of CNS
strabismus
straight sinus
streptococcal infection
streptococcus viridans
stress, emotional
striatal encephalitis
striatonigral degeneration
striatonigral degeneration, infantile
striatum, lesion of
striatum, lesion of, bilateral
striopallidodentate calcifications, familial idiopathic
strokelike episodes
stuporous
Sturge-Weber syndrome
stuttering
subarachnoid hemorrhage
subarachnoid hemorrhage, familial
subarachnoid hemorrhage, prognosis
subarachnoid hemorrhage, recurrent
subcortical U fibers
subdural hematoma
subependymal nodules
substance P
substantia nigra
subthalamic nucleus
subthalamic nucleus deep brain stimulation
succinate dehydrogenase deficiency
suck reflex
suck, poor
sudden death
sudden infant death syndrome
suicide
sulfite oxidase deficiency
superior sagittal sinus thrombosis
superoxide dismutase
suprascapular neuropathy
sural nerve
survival motor neuron gene
swallow evaluation
sweating
sweating, abnormality of
symmetric brain lesions
sympathetic nervous system
syncope
syncope, recurrent
syncope, triggers of
syndactyly
synkinesis
synophrys
syringobulbia
syringomyelia
syringomyelia, familial
systemic illness
systemic lupus erythematosus
systemic lupus erythematosus, neurologic complications with
T cell lymphoma
tachycardia
tachypnea
tandem gait, ataxic
Tangier's disease
tapetoretinal degeneration
tardive dystonia
tau protein
tauopathy
Tay-Sachs disease
TDP-43 proteinopathy
teeth, abnormal
teeth, number of in infants
teeth, wide-spaced
telangiectases
telangiectases, retinal
temozolomide
temper tantrums
temporal artery, biopsy
temporal lobe, atrophy
temporal lobe, lesion
temporal lobe, lesion, bilateral
temporalis muscle wasting
temporalis muscle weakness
temporomandibular joint
temporomandibular joint, dislocation
temporomandibular joint, pain
tendon, enlarged
tensilon test
tensilon test, false negative
tension headache
tentorium cerebelli
teratogenesis
teratogenic drugs
term infant
testicular atrophy
testicular biopsy
testicular enlargement
tetany
tetrahydrobiopterin
thalamotomy
thalamus, focused ultrasound ablation
thalamus, atrophy of
thalamus, lesion of
thalamus, lesion of-bilateral
thalassemia
thalassemia/mental retardation syndrome
thiamine
thiazide diuretic
third nerve palsy
thromboangiitis obliterans cerebri
thrombocytopenia
thrombophlebitis
thrombotic microangiopathy
thrombotic thrombocytopenia purpura
thymoma
thyroid function tests
thyrotoxicosis
thyroxine
tic
tic, chronic multiple
tinnitus
tinnitus, pulsatile
tissue plasminogen activator, intravenous
titinopathy
titubation
tocainide
toe walking
tolazamide
tomaculous neuropathy
tone, muscle, increased
tongue, atrophy
tongue, biting
tongue, discoloration
tongue, enlarged
tongue, fasciculations of
tongue, protrusion of
tongue, red papules
tongue, weakness
tonic foot response
tonic spasms
tonsillitis
topiramate
torsades de points
torticollis
torticollis, familial
torticollis, post traumatic
toxins, nervous system
transient global amnesia
transient ischemic attack
transient ischemic attack, recurrent
transient neurologic deficit
transketolase
transverse smile
trauma
travel, foreign
treatment of neurologic disorder
treatment resistant
tremor
tremor, cerebellar
tremor, intention
tremor, jaw
tremor, leg
tremor, postural
tremor, resting
tremor, surgical treatment of
tremor, thalamic stimulation for suppression of
tremor, treatment of
tremor, voice
tremor, wing beating
tremor, writing
tremulousness
trichopoliodystrophy
tricresylphosphate
trientine dihydrochloride
trigeminal nerve
trigeminal nerve, lesion of
trigeminal neuralgia
trigeminal neuralgia, familial
trigeminal neuropathy
trigeminovascular system
trinucleotide repeats
tripping
trisomes
trisomy 18
trisomy 9p
trochlear nerve
trochlear nerve palsy
tuber, cortical
tuberin
tuberous sclerosis
tuberous sclerosis, screening for
tubular aggregates, muscle
tubulopathy
tumor suppressor gene
Turcot syndrome
Turner's syndrome
twins
type 1 muscle fiber
type 2 muscle fiber
tyrosine
tyrosine hydroxylase deficiency
tyrosinemia
ubiquilin 1
ulcerative colitis
ulnar neuropathy
ultrasonography
ultrasonography, carotid artery
ultrasonography, head
ultrasonography, head, fetus-neonate
ultrasonography, nerve
umbilical-cord blood transplantation
uncal herniation
unconsciousness
unconsciousness, transient
undiagnosed
Unverricht-Lundborg disease
upgaze, paralysis of
upright-tilt test
urea-cycle enzymopathies
uremia
uric acid, low
urinalysis, abnormal
urinary casts
urinary catecholamines
urinary incontinence
urinary sulfatidase excretion
urinary urgency
urine test for metabolic disorders
urine, dark
Usher's syndrome
uveitis
vaccine
valvulopathy
vanadium
vanishing white matter
varicella zoster virus
varicella zoster virus, encephalitis
varicose veins
vasculitides
vasculopathy
vasovagal episode
vegetarianism
vein of Galen
Vemurafenib
venous hemangioma
venous thrombosis, non-cerebral
ventricular enlargement
ventricular garlands
ventricular septal defect
ventricular tachycardia
ventriculostomy, endoscopic
verapamil
vertebral-basilar insufficiency
vertigo
vertigo, episodic
vertigo, migraine causing
vertigo, treatment of
very long chain fatty acids
vestibular function, tests of
vestibulopathy
vibratory sensation
vibratory sensation, abnormal
violent behavior
viral infection
viral infection, CNS
viral isolation
Virchow-Robin spaces, dilated
visceral neuropathy
vision loss, sequential
vision, blurred
vision, failure of in childhood
visual acuity
visual acuity, decreased
visual acuity, decreased, monocular
visual evoked response
visual field defect
visual field testing
visual fields, constricted
visual impairment
visual loss
visual loss, congenital
visual loss, progressive
visual loss, slow
visual loss, sudden
visual loss, transient
visual obscurations, transient
visual tracking
visuospatial disturbance
vital capacity
vitamin A
vitamin deficiency
vitamin E
vitamin E deficiency
vitamin K
vitamin supplementation
vitamin, multiple
vitiligo
vitreous opacities
voice, abnormality of
vomiting, recurrent
Von Hippel Lindau
Von Hippel Lindau, carrier
Von Hippel Lindau, screening protocol for
von Hippel-Lindau, screening
Walker-Warburg syndrome
walking
walking frame
walking, delayed
walking, difficulty with
water channel antibodies
weakness
weakness, acute
weakness, chronic
weakness, episodic
weakness, fatiguable
weakness, fluctuating
weakness, focal
weakness, generalized
weakness, infant
weakness, progressive
weakness, proximal
weaning from respirator, failure to
web sites
weight loss
Werdnig-Hoffman disease
Wernicke's aphasia
Wernicke's encephalopathy
West disease
Western immunoblot test
wheelchair
Whipple's disease
whistle, inability to
white freckles
white matter disease
white matter disease, location
white matter disease, pattern
white matter disease, subcortical
white matter disease, unilateral
wide based gait
Wildervanck's syndrome
Williams syndrome
winging of scapula
Wiskott-Aldrich syndrome
Wolfram syndrome
Wood's light
word-finding difficulty
workup
wound healing, poor
wrist drop
writers cramp
writing
xanthelasma
xanthoma, tendon
xeroderma pigmentosa
xerophthalmia
X-linked bulbospinal neuronopathy
X-linked dystonia-parkinsonism syndrome
x-linked hydrocephalus
x-linked intellectual deficit
X-linked lissencephaly
x-linked mental retardation
X-linked myopathy
x-linked myopathy with excessive autophagy
X-linked neuropathy
x-ray, cervical spine
Zika virus infection
zinc
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Adult Patient Presenting with Spine Pain Following a Motor Vehicle Accident
Neurol 100:1025-1031, Sharma,V. & Soto,O, 2023

Paroxysmal Exercise-Induced Dyskinesias Due to Pyruvate Dehydrogenase Deficiency
Neurol 101:46-49, deGusmao,C.M.,et al, 2023

Clinicopathologic Conference, Facioscapulohumeral Muscular Dystrophy
NEJM 388:2379-2387, Case 19-2023, 2023

Current and Emerging Issues in Wilsons Disease
NEJM 389:922-938, Roberts,E.A. & Schilsky, M.L., 2023

Focusing on the Eye Signs of Alport Syndrome in a 40-Year-Old Man Who Previously Had a Kidney Transplant and Hearing Loss
Lancet 401:e2, Kovalchuk,B. & Khoramnia,R., 2023

Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
JAMA Neurol 80:107-108, Bernaola,M.T.,et al, 2023

A Young Adult Man with Cognitive Changes, Gait Difficulty, and Renal Insufficiency
Neurol 100:206-212, Stamm,B.,et al, 2023

A 23-Year-Old Woman Presenting with Cognitive Impairment and Gait Disturbance
Neurol 99:997-1003, Chaity,D.K.,et al, 2022

Updates on Sturge-Weber Syndrome
Stroke 53:3769-3779, Yeom,S.E.&Comi,A.M., 2022

Spinal Muscular Atrophy
UpToDate, Oct, Bodamer,O.A., 2022

A 36-Year-Old Man With Asymmetric Muscle Weakness
Neurol 99"1057-1061, Harada,Y.,et al, 2022

Unilateral Leukoencephalopathy Revealing Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
Ann Neurol 91:889-890, Gollion, C.,et al, 2022

Bilateral Hearing Loss and Constricted Visual Fields
BMJ 378:e070672, Sachdeva, G. & Shafquat, S., 2022

More Than a Little Unsteady
NEJM 387:e9, Kraft, A.W.,et al, 2022

Clinicopathological Conference, Chronic Candida Albicans Meningitis
NEJM 387:641-650, Case 25-2022, 2022

Fragile X-Associated Tremor or Ataxia Syndrome in a Patient with Difficulty Walking, Falls, a Tremor, and Erectile Dysfunction
Lancet 400:1144, Sabino de Oliveira, D.,et al, 2022

Amyotrophic Lateral Sclerosis
Lancet 400:1363-1380, Feldman, E.L.,et al, 2022

Spectrum of Neuroradiologic Findings Associated with Monogenic Interferonopathies
AJNR 43:2-10, Benjamin, P.,et al, 2022

Multiple Cranial Nerve Gadolinium Enhancement in Norrie Disease
Ann Neurol 91:158-159, Jokela, M.,et al, 2022

A 31-Year-Old Man with Sequential Vision Loss
Neurol 98:163-169, Fortes, B.,et al, 2022

Thyrotoxic Periodic Paralysis
UptoDate Jan, Gutmann, L. & Conwit, R., 2022

A 6-Year-Old Girl with Progressive Toe Walking
Neurol 98:e769-e773, Libdeh, A.A. & Ibrahim, A., 2022

Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
NEJM 386;674-687, Case 5-2022, 2022

Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis
UptoDate 2022 Jan, Darras, B.T., 2022

Leber Hereditary Optic Neuropathy with Longitudinal Spinal Cord Lesion Mimicking Spinal Cord Infarction
Neurol 98:468-469, Zhao, B.,et al, 2022

Multicenter Consensus Approach to Evaluation of Neonatal Hypotonia in the Genomic Era
JAMA Neurol 79:405-413, Morton, S.U.,et al, 2022

Brain Tumors in Children
NEJM 386:1922-1931, Cohen, A.R., 2022

Sturge-Weber Syndrome
www.UptoDate.com,Dec, Patterson,M.C., 2022

"Disappearing Infarct" Is Late-Onset MELAS
Ann Neurol 90:1001-1002, Landis,T.M.,et al, 2021

Hypotonia and Delayed Teeth Eruption in a 2-Year-Old Girl
Neurol 97:875-878, Dinov, D.,et al, 2021

A 28-Year-Old Woman with Vision Loss and an Unusual Gait
Neurol 97:e1860-e1865, Dohlman, J.C.,et al, 2021

A 59-Year-Old Man with Progressive Proximal Weakness Since Childhood
Neurol 97:958-963, Davalos, L.,et al, 2021

A 6-Year-Old Boy with Muscle Twitching
Neurol 96:e301-e304, Lewis, H.S.,et al, 2021

Molecular Diagnostic Yield of Exome Sequencing in Patients with Cerebral Palsy
JAMA 325:467-475, Moreno-De-Luca, A.,et al, 2021

A Middle-aged Woman with Severe Scoliosis and Encephalopathy
JAMA Neurol 78:251-252, Mohan, G.,et al, 2021

Bilateral Temporal Pole Involvement in Adult-Onset X-Linked Adrenoleukodystrophy
JAMA Neurol 78:367-368, Liu, M.,et al, 2021

Brain and Skin Involvement in Erdheim-Chester Disease
Neurol 96:e1590-e1592, Budhram, A.,et al, 2021

Alzheimers Disease
Lancet 397:1577-1590, Scheltens, P.,et al, 2021



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