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Differential
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abdominal distention
abdominal reflex, absent
abducens nerve paralysis
abscess, intracerebral
acanthocytosis
acanthosis nigricans
acetazolamide
acetylcholine
achilles tendon, enlarged
acoustic nerve
acoustic neurinoma, bilateral
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome myelopathy
acromicria
acyl CoA dehydrogenase deficiency
Addison's disease
adrenoleukodystrophy
adrenoleukodystrophy, carrier
adrenomyeloneuropathy
adult polyglucosan body disease
adult-onset leukodystrophy, with neuroaxonal spheroids
advances in neurology
adverse drug reaction
Africa
aggression
akathisia
akinetic mute
albinism
alcohol
alcohol intolerance
alcohol, neurologic complications with
alcoholism
Alexanders disease
Alexanders disease, adult onset
algorithm
alkylating agents
alopecia
alpha-fetoprotein
altered states of consciousness
alternating rapid movement
alternating rapid movement, impaired
Alzheimer's disease
aminoacidopathies
aminoacidurias
amniocentesis
amyloid plaques
amyotrophic lateral sclerosis
anemia
Angelman syndrome
aniridia
ankle edema
ankle reflex, absent
anosmia
anterior horn cell disease
anterior tibial muscle weakness
antibodies to voltage-gated calcium channels
anticholinergic drugs
anticholinesterase
anticonvulsants
anticonvulsants, effectiveness
anticonvulsants, selection of
antimetabolite
antioxidant
anxiety
aphasia
apnea
apnea, primary central
apraxia
apraxia of eye movements
areflexia
arm weakness
Arnold Chiari malformation
arrhythmia, cardiac
arterial dissection, carotid
arterial dissection, multiple
arteriovenous malformation
arteriovenous malformation, pulmonary
arylsulfatase A
ascites
asparginase
aspiration
astrogliopathy
asymptomatic
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
atonic bladder
ATP1A3 gene
attention span
atypical
auditory evoked brainstem potentials
autism
autoimmune disease
autonomic dysfunction
autosomal rcessive spastic ataxia of Charlevoix-Saguenay
axonal spheroid
B 12 deficiency
Babinski sign
baclofen
bacterial infection
basal ganglia
basal ganglia, calcification of
basal ganglia, degeneration
basal ganglia, lesion of
basal ganglia, lesion, bilateral
Bassen-Kornzweig syndrome
behavior, combative
behavioral disorder
benign essential tremor
biologic markers
biopterin deficiency
biotin deficiency
biotinidase deficiency
bladder dysfunction
blindness
blinking, reduced
blood dyscrasias, neurologic findings with
bone marrow biopsy
brachycephaly
bradykinesia
brain atrophy
brain biopsy
brain biopsy, stereotaxic
brainstem, atrophy
brainstem, lesion of
brainstem, neoplasms of
Brown-Vialetto-Van Laere syndrome
bulbar palsy
cachexia
cafe au lait spots
CAG repeats
calcification, intracranial
calcium channel dysfunction
calf hypertrophy
camptocormia
cane
carbamazepine
carcinoembryonic antigen
carcinoma
cardiomyopathy
carotid artery disease
CAT scan
CAT scan, abnormal
CAT scan, chest
CAT scan, emission
CAT scan, emission, abnormal
cataplexy
cataracts
cataracts, congenital
caudate nucleus, atrophy
caudate nucleus, lesion of, bilateral
celiac disease, adult
central core disease
cerebellar ataxia, autosomal recessive
cerebellar ataxia, children
cerebellar ataxia, children, differential diagnosis of
cerebellar ataxia, hereditary
cerebellar ataxia, neuropathy and vestibular areflexia syndrome
cerebellar ataxia, primary
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar hemangioma
cerebellar hypoplasia
cerebellar lesion
cerebellar plaques, amyloid
cerebellar vermis
cerebellum
cerebellum, disease of
cerebellum, neoplasms of
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 infarction, subcortical
cerebral palsy
cerebro hepato renal syndrome
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, pressure low
cerebrospinal fluid, xanthochromia of
cerebrotendinous xanthomatosis
cerebrovascular accident
cerebrovascular accident, genetic
cerebrovascular accident, mimics
cerebrovascular accident, recurrent
cerebrovascular accident, young adult
ceruloplasmin, serum
cervical spondylosis
channelopathy
Charcot-Marie-Tooth
Chediak-Higashi syndrome
chemotherapy, CNS treatment and complications with
cherry red spot-myoclonus syndrome
chewing movements
children
chloride channel dysfunction
choking
cholestanol
chorea
chorea, causes of
chorea, familial
choreoathetosis
chromosomal abnormality
chromosome 11
chromosome 12
chromosome 14
chromosome 15
chromosome 18
chromosome 19
chromosome 2
chromosome 20
chromosome 21
chromosome 6
chromosome 9
chronic progressive external ophthalmoplegia
ciguatera poisoning
cirrhosis
cisterna magna, enlarged
Clinical Pathologic Conference(C.P.C.)
clonus
clubfoot as related to neurologic disease
Coats syndrome
cobalamin C deficiency
Cockayne's syndrome
coenzyme Q10 deficiency
cognition
cognition, slowed
cogwheel rigidty
cold hands sign
Collier's sign
color vision, impaired
coma
coma, episodic
complications
cone-rod dystrophy
confabulation
congenital myopathy
congestive heart failure
conjunctival biopsy
conjunctivitis
consanguinity
constipation
contractures, joint
controversies in neurology
conus medullaris, lesion of
copper metabolism, abnormal
cornea, abnormal
corpus callosum
corpus callosum, atrophy of
corpus callosum, lesion of
corpus callosum, thinning
cortical blindness
cough
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
cranio-cervical junction
C-reactive protein, elevated
creatine phosphokinase(CPK)elevated
Creutzfeldt-Jakob disease, genetic
crossed adductor reflex
cry, abnormal
cry, weak
Cuba
cultured skin fibroblasts
cyclic vomiting
cyst
cyst, peritumoral
cyst, neoplastic cerebellum
deafmute
deafness
deep gray nuclei
deep tendon reflexes
degenerative diseases of CNS
delay in diagnosis
delayed dentition
dementia
dementia, childhood
dementia, familial
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
dementia, transmissible
demyelinating disease
dental procedure, neurologic complications with
dentate nuclei, lesion of
dentatorubral-pallidoluysian atrophy
depression
dermatoglyphics
developmental disability
developmental milestones
developmental milestones, loss of
developmental retardation
dexterity, impaired
diabetes insipidus
diabetes mellitus
diabetes mellitus, chemical
diabetes mellitus, neurologic manifestations of
diagnostic criteria
diaphragmatic paralysis
diarrhea
diet
differential diagnosis
difficulty climbing stairs
dilantin
diplopia
disability, neurological
distal muscle atrophy
distal muscle weakness
diurnal variation
dizziness
DNA probes
dopa responsive dystonia
dopamine agonist
down-beat nystagmus
down-beat nystagmus, primary position of gaze
Dravet syndrome
drooling
dropped head syndrome
drug abuse, inhalation
drug induced neurologic disorders
dwarfism
dysarthria
dysdiadochokinesia
dysmetria
dysmorphic
dysphagia
dyspnea
dyspraxia
dyssynergia cerebellaris myoclonica
dystonia
dystonia musculorum deformens
dystonia, focal
dystonia, treatment of
dystrophin
EAST syndrome
eating disorder
edema, pedal
electrical sensation
electrocardiogram, abnormal
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
electron microscopy
electronystagmography
electroretinograph
ELISA
emergency room
encephalitis
encephalitis, viral
encephalopathy
encephalopathy, progressive
endemic area
enzyme, defect
enzyme, muscle disease
epicanthal folds
epidemiology of neurology
epileptic encephalopathy
episodic disorders
episodic neurologic deficits
epistaxis
equinovarus
erectile dysfunction
esophageal varices
ethics in neurology
evoked potentials
excitotoxin
exercise
exercise intolerance
exome sequencing
extraocular muscle lesion
eye movement, disorders of
Fabry's disease
facial appearance, abnormal
facial expression abnormality
facial nerve palsy, bilateral
facial pain
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
failure to thrive
falling
false negative
familial
familial hemiplegic migraine
familial periodic ataxia
family planning
FARS2 deficiency
fasciculation
fatal familial insomnia
fatigue
fatty acid, elevated plasma content
feeding disorder
fever
fine motor function, impaired
finger nose finger test
finger tapping
fingerprint bodies
fish
fistula, arterio-venous, pulmonary
fluorescene in situ hybridization
fluorouracil
flush syndrome
foam cells
foot deformity
foot drop
foot drop, bilateral
fornix, lesion of
Fragile-X associated tremor/ataxia-syndrome
fragile-X syndrome
fragile-X syndrome, carrier
frataxin
Friedreich's ataxia
Friedreich's ataxia, late onset
frontotemporal dementia, behavioral variant
fundus, abnormality of
gadolinium
gait disorder
gait, apraxic
gait, festinating
gait, spastic
gait, waddling
galactosemia
gangliosidosis GM1
gargoylism
gastrointestinal disease, neurologic complications
gastrointestinal motility
gastroparesis
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gender
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
genu of corpus callosum
geographic location
Gerstmann-Straussler-Scheinker disease
GFAP gene
Gillespie syndrome
glabellar sign
glaucoma
gliosis
globus pallidus
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glucose tolerance test, abnormal
GLUT1 deficiency syndrome
glutamate dehydrogenase deficiency
glutamic acid
glycogen storage disease
gout
Gowers maneuver
granular osmiphilic material
gray hair
grimacing
growth hormone deficiency
growth retardation
Guillain Barre syndrome
Hallervorden Spatz disease
Hallervorden Spatz disease, late onset
Hallgren's syndrome
hallucination
hammertoes
hand clapping
hand deformity
hand flapping
hand wringing
handwriting
head injury
head nodding
headache
headache, sudden onset of
headache, throbbing
hearing loss
hearing problems in children
heart block
heel-knee-shin test
hemangioblastoma
hematuria, gross
hemidiaphragm, paralysis of
hemiparesis
hemiplegia
hemochromatosis
hemochromatosis, primary
hemophagocytic lymphohistiocytosis, cerebromeningeal
hemophagocytosis
hepatic encephalopathy
hepatic failure
hepatitis
hepatolenticular degeneration(Wilson's disease)
hepatolenticular degeneration(Wilson's disease), presymptomatic
hepatolenticular degeneration(Wilson's disease), screening for
hepatolenticular degeneration, non-Wilsonian
hepatomegaly
hepatosplenomegaly
heralding manifestation
hereditary hemorrhagic telangiectasia(HHT)
hereditary myopathy with early respiratory failure
herniated disc, thoracic
HLA
homocystinuria
hot cross bun sign
human T-lymphotropic virus type I(HTLV-I)
human T-lymphotropic virus type II(HTLV-II)
huntingtin
Huntington's chorea
Huntington's chorea, late onset
Huntington's chorea, misdiagnosis of
Huntington's disease, children
Hurler's syndrome
hydrocephalus
hydroxytryptophan L-5(L-5 HTP)
hyperactivity
hyperammonemic encephalopathy
hyperglycemia
hyperhidrosis
hyperhomocysteinemia
hyperphagia
hyperpigmentation of skin
hyperreflexia
hypertension
hyperthermia
hyperthyroidism
hypertonia
hypertriglyceridemia
hypoalbuminemia
hypocholesterolemia
hypodontia
hypofibrinogenemia
hypogonadism
hypokalemia
hypokalemic periodic paralysis
hypometric saccades
hypomyelination
hyponatremia
hypopigmentation of skin
hyporeflexia
hyposmia
hypotonia
hypotonia, infants
hypoxia
iatrogenic neurologic disorders
imbalance
imbalance, postural
immunodeficiency
immunohistochemistry
immunologic disease
immunosuppression
impotence
impulsivity
inability to sit up
inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with
inappropriate behavior
inattention
inborn errors of metabolism
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, eosinophilic intranuclear
inclusion bodies, intracytopasmic
inclusion bodies, intranuclear
inclusion bodies, ubiquitin
incontinence, fecal
incoordination
infection
insight, loss
insomnia
insulin resistance
intellectual deficit
intellectual deterioration
internal capsule
internuclear ophthalmoplegia
internuclear ophthalmoplegia, bilateral
intestinal pseudoobstruction
intracerebral hemorrhage
intracranial pressure, increased
iris, abnormal
iron, brain
irritability
isoniazid
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
jaundice
jaw pain
Jewish
karyotyping
Kayser-Fleischer ring
Kearns-Sayre syndrome
keratoconus
kinesia paradoxica
Korsakoff's psychosis
kyphoscoliosis, neurologic causes of
kyphosis
lactic acidemia
lacunar infarction
Lafora's disease
lathyrism
laughing, pathologic
Laurence-Moon-Bardet-Biedl syndrome
L-dopa
learning disability
learning disability, in children
Leber's hereditary optic neuropathy
leg weakness, bilateral
Leigh's disease
Leigh's disease, adult variety
lenticular nucleus, lesion of, bilateral
leukemia
leukemia, neurologic findings assoc.with
leukocyte enzyme abnormality
leukocyte peroxidase
leukocytosis
leukodystrophy
leukoencephalopathy
leukoencephalopathy, adult onset, sporadic
leukoencephalopathy, differential diagnosis
leukoencephalopathy, hereditary diffuse
leukopenia
Lewy body
Lhermitte's sign
libido, decreased
lid closure, weakness of
life expectancy
linear lesion
lipid storage disorder of CNS
lipid storage myopathy
liver disease
liver function enzymes
liver transplantation
lordosis
lymphadenopathy
lymphoma
lysosomal storage disease
macrocephaly
macrognathia
macular degeneration
Maghreb
malabsorption
malformation, CNS, congenital
malignant hyperpyrexia
maple syrup urine disease
marche a petits pas
Marinesco-Sjogren syndrome
masked facies
MELAS syndrome
memory, defect of recent
memory, impairment of
meningismus
meningitis, CSF cell count-normal
meningoencephalopathy
mental retardation
MERRF syndrome
mesial temporal lobe
metabolic acidosis
metabolic disorder, primary
metachromatic leukodystrophy
metachromatic leukodystrophy, adult onset
metachromatic leukodystrophy, juvenile
methotrexate
methylhydrazine derivatives
methylmalonic acidemia
Mexican
microcephaly
microdontia
micrographia
microhemorrhage, intracerebral
midbrain, atrophy
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
migraine
migraine, hemiplegic
mimics
Minamata disease
mirror writing
misdiagnosis
mitochondrial disease
mitochondrial disease, pathogenesis
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
monoamine oxidase inhibitors
monoparesis
mood change
mortality
motor cortex
motor neuron disease
movement disorder
movement disorder, extrapyramidal
movement disorder, treatment of
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, eye of tiger sign
MRI, FLAIR
MRI, high signal intensity of basal ganglia
MRI, muscle
MRI, negative
MRI, paramagnetic effect
MRI, perfusion
MRI, punctate pattern
MRI, serial
MRI, spinal cord
MRI, spine
MRI, susceptibility weighted
MRI, T1 weighted high signal foci
MRS
mucopolysaccharidoses
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, misdiagnosis
multiple system atrophy
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle pain
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, cardiovascular changes with
muscular dystrophy, central nervous system abnormality
muscular dystrophy, differential diagnosis of
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
mutism
myasthenic syndrome
myelomalacia
myeloneuropathy
myelopathy
myelopathy, chronic progressive
myelopathy, hepatic
myelopathy, vacuolar
myoclonic jerks
myoclonus
myoclonus, cortical
myoclonus, epilepsy
myoclonus, stimulus sensitive
myoglobinuria
myokymia
myopathy
myopathy, distal
myopathy, distal Laing
myopathy, genetic
myopathy, hereditary
myopathy, metabolic
myopathy, mitochondrial
myopathy, vacuolar
myopia
myotonia
myotonia congenita
myotonia dystrophica
N-acetylcysteine
Native Americans
nausea and vomiting
neck weakness
negative
neonatal screening, genetic neurologic disorders
neoplasm, metastatic to CNS
neoplasm, primary intracranial
neoplasm, primary of CNS
neoplasm, primary of CNS-surgical treatment of
nerve biopsy
nerve conduction studies
nerve growth factor
neuritis
neuroaxonal dystrophy
neuroaxonal dystrophy, infantile
neuroaxonal dystrophy, juvenile
neuroaxonal leukodystrophy
neurocutaneous disease
neuroendocrinology
neurofibrillary degeneration
neurofibromatosis 1
neurogenic bladder
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic disease, tempo
neurologic examination
neurologic examination, focal
neurologic signs
neurologic symptoms
neurologic testing
neuromuscular disease, electrodiagnosis of
neuromyotonia
neuronal ceroid-lipofuscinosis
neuronal intranuclear inclusion disease
neuronal migration disorder
neuronopathy
neuronopathy, sensory
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
neuropathy, amyloid
neuropathy, ataxia, retinitis pigmentosa
neuropathy, ataxic
neuropathy, hereditary peripheral
neuropathy, hypertrophic
neuropathy, onion bulb
neuropathy, peripheral
neuropathy, sensory
neurotoxin
neurotransmitter
neutropenia
next-generation sequencing
Niemann-Pick disease
night blindness
nitrogen mustard
nitrous oxide
NOTCH2NLC
nutritional deficiency
nystagmus
nystagmus, gaze-evoked
nystagmus, gaze-paretic
nystagmus, hereditary
nystagmus, periodic
nystagmus, primary position of gaze
nystagmus, rotary
nystagmus, upbeating-in primary position of gaze
nystagmus, vertical
obesity
ochronosis
ocular motility, disorders of
ocular myopathy
oculodentodigital dysplasia
old age, neurology of
ophthalmoplegia
ophthalmoplegia, progressive external
opisthotonus
optic atrophy
optic atrophy, hereditary
optic nerve
optic neuropathy
optical coherence tomography
optokinetic nystagmus, abnormal
orbit, tomograms of
orthopnea
orthostatic hypotension
oscillopsia
osteoarthrosis
osteoporosis
pain
pain, abdominal
pain, foot
pain, leg
palatal myoclonus
palilalia
pancytopenia
PANK2 mutation
papilledema
paralysis
paramyotonia congenita
paranoia
paraparesis
paraparesis, familial spastic
paraparesis, familial spastic, classification
paraparesis, spastic
paraparesis, spastic, tropical
paraplegia
paraplegin
paresthesias
Parkinson disease
Parkinson disease, differential diagnosis of
Parkinson disease, familial
Parkinson disease, freezing phenomena in
Parkinson disease, juvenile
Parkinson disease, pathogenesis of
Parkinson disease, surgical treatment of
Parkinson disease, treatment of
Parkinsonism multiple-system atrophy
Parkinsonism syndrome
paroxysmal neurologic deficits
PAS positive
PAS positive material in the brain
past pointing
pathology
patient information and support
Pelizaeus Merzbacher
penicillamine
periodic paralysis
peroxisomal disease
personality change
pes cavus
pheochromocytoma
phlebotomy
photophobia
photosensitivity, skin
physostigmine
phytanic acid
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
pneumonia
poison, mercury
poison, neurologic problems with
POLG1 gene
POLR3B
polydactyly
polyglucosan body
polyglucosan body disease
polymerase chain reaction
polyneuropathy
pons, atrophy
pons, lesion of
pontocerebellar atrophy
portal caval shunt
positional head-hanging test
postural abnormality
potassium channel antibodies
potassium channel dysfunction
Prader-Labhart-Willi syndrome
precipitating factors
pregnancy, neurologic complications in
prenatal diagnosis by amniocentesis
pretectal syndrome
prevention of neurologic disorders
primary episodic ataxia
primary lateral sclerosis
prion disease
prion protein gene
prisoners of war, neurologic complications in
procarbazine
progeria
prognathism
prognosis
progressive infantile poliodystrophy
progressive myoclonic epilepsy
progressive neurologic disorder
progressive pallidum atrophy
proprioception, abnormal
protein 14-3-3, cerebrospinal fluid
proteinuria
proximal muscle atrophy
pseudobulbar palsy
pseudohypertrophy
pseudoretinitis pigmentosa
pseudoxanthoma elasticum
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychological testing, neurologic problems
psychomotor retardation
psychosis
ptosis
ptosis, bilateral
pulmonary embolism
Purkinje cell
pursuit eye movements, abnormal
putamen, lesion of
putamen, lesion of, bilateral
pyramidal
pyramidal tract
pyramidal tract dysfunction
pyruvate metabolism, abnormality of
quadriparesis
quadriplegia
radiation hypersensitivity
radiation therapy, CNS treatment and complications with
radiation therapy, stereotactic
ragged-red fibers
rapidly progressing neurologic illness
rash
reading disorder, acquired
real-time quaking-induced conversion
Red flags
refractive errors
Refsum's disease
rehabilitation for neurologic disorders
remote effect of cancer on the nervous system
renal failure
renal stones
renal tubular acidosis
respiratory failure
reticulum cell sarcoma
retina, abnormal
retinal degeneration
retinal hemangioma
retinal lesion
retinitis pigmentosa
retinopathy
Rett's syndrome
reversible neurologic disorder
review article
rhabdomyolysis
riboflavin
riboflavin transporter deficiency
rigidity
Riley-Day syndrome
risk factors
Romberg's sign
Rosenthal fibers
saccadic eye movements, abnormal
salivation, excessive
schizophrenia
scissors gait
sclerae, hyperpigmented
SCN1A gene
scoliosis
scoliosis, neurologic association with
screaming
screening
sea-blue histiocytes
seizure
seizure, children
seizure, familial
seizure, febrile
seizure, intractable
seizure, neonatal
seizure, paradoxical
seizure, photosensitive
seizure, psychomotor-temporal lobe
seizure, tonic-clonic
seizure, treatment of
self-mutilation
semialdehyde dehydrogenase deficiency
sensorineural hearing loss
sensory ganglia
sensory ganglia, abnormal
sensory loss
serologic testing
short stature
Shy-Drager syndrome
sinemet
skin, biopsy
skin, darkening of
skin, lesions in neurologic disorders
sleep apnea
sleep pathology and physiology
slit lamp examination
sloped shoulders
slurred speech
small vessel disease
smiling
sodium channel dysfunction
somatosensory evoked potentials
spartin
spastic ataxia
spastic diplegia
spastic paraplegia, type 7
spasticity
spastin
speech disorder
speech disorder, childhood
speech disorder, non aphasic
speech, delayed development of
speech, loss of
speech, soft
sphingolipodoses
Spielmeyer Vogt syndrome
spinal cord
spinal cord, lesion of
spinal cord, neoplasm
spinal cord, pathologic exam of
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, intermediate form
spinal xanthomatosis
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
splenomegaly
spondylolysis
spongy degeneration of brain
staggering
stare
startle myoclonus
status epilepticus
steatorrhea
steppage gait
stereotaxic surgery
stereotyped behavior
stereotypy
steroid therapy, CNS treatment and complications with
stiff legs
storage disease of CNS
strabismus
stress, emotional
striatonigral degeneration
striatonigral degeneration, infantile
striatum, lesion of
striopallidodentate calcifications, familial idiopathic
strokelike episodes
stuttering
subarachnoid hemorrhage
substantia nigra
suck, poor
sudden death
suicide
survival motor neuron gene
symmetric brain lesions
syndactyly
syphilis, neurologic complications with
systemic illness
tachycardia
tandem gait, ataxic
tapetoretinal degeneration
tauopathy
Tay-Sachs disease
teeth, abnormal
teeth, number of in infants
teeth, wide-spaced
telangiectases
temper tantrums
temporal lobe, lesion
tendon, enlarged
term infant
tetrahydrobiopterin
thalamus
thalamus, lesion of
thalamus, lesion of-bilateral
thrombocytopenia
thrombophlebitis
tinnitus
titinopathy
titubation
toe walking
tongue, protrusion of
tonic foot response
topiramate
toxins, nervous system
transient ischemic attack
transient ischemic attack, recurrent
transient neurologic deficit
transverse smile
trazodone
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, intention
tremor, postural
tremor, resting
tremulousness
trientine dihydrochloride
trinucleotide repeats
tripping
trisomes
trisomy 9p
tubulopathy
twins
undiagnosed
Unverricht-Lundborg disease
upgaze, paralysis of
urea-cycle enzymopathies
urinary frequency
urinary incontinence
urinary urgency
urine test for metabolic disorders
urine, dark
Usher's syndrome
vasculopathy
venous thrombosis, non-cerebral
vertigo
vertigo, episodic
vertigo, treatment of
vestibulopathy
vibratory sensation, abnormal
vinblastine
vincristine neurotoxicity
violent behavior
viral isolation
vision, failure of in childhood
visual acuity, decreased
visual evoked response
visual field defect
visual fields, constricted
visual loss
visual loss, progressive
visual loss, slow
vital capacity
vitamin A
vitamin deficiency
vitamin E
vitamin E deficiency
vitamin K
vitamin supplementation
vitiligo
vocal cord paralysis
voice, abnormality of
Von Hippel Lindau
walking
walking frame
walking, difficulty with
war
weakness
weakness, acute
weakness, focal
weakness, generalized
weakness, progressive
weakness, proximal
weaning from respirator, failure to
web sites
weight loss
Western immunoblot test
wheelchair
white matter disease
white matter disease, subcortical
wide based gait
winging of scapula
Wolfram syndrome
work loss
workup
wrist drop
writing
xanthoma, tendon
xeroderma pigmentosa
X-linked bulbospinal neuronopathy
zinc
Showing articles 0 to 50 of 2698 Next >>

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

Neuroimaging Features of Biotinidase Deficiency
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Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
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A 48-Year-Old Man With Spasticity and Progressive Ataxia
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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

A 6-Year-Old Girl with Progressive Toe Walking
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Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
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More Than a Little Unsteady
NEJM 387:e9, Kraft, A.W.,et al, 2022

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 Middle-Aged Man with Progressive Gait Abnormalities
Neurol 97:e2423-e2428, Lin, J.,et al, 2021

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

Cervical Spondylotic Myelopathy Secondary to Ochronotic Vertebral Arthropathy
Neurol 96:627-628, Pinto, W.,et al, 2021

Clinicopathologic Conference, Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome
NEJM 385:165-175, Case 20-2021, 2021

A 72-year-old Man with a Progressive Cognitive and Cerebellar Syndrome
Neurol 95:e2707-e2710, Lad, M. & Griffiths, T.D., 2020

Hypointensity of the Basal Ganglia in Adults with Glucose Transporter Protein Type 1 Deficiency Syndrome: A Novel Magnetic Resonance Imaging Finding
Ann Neurol 87:10-11, Van Samkar, A.,et al, 2020

Duchenne Muscular Dystrophy
BMJ 368:L7012, Fox, H.,et al, 2020

A 45-Year-Old Man with Progressive Insomia and Psychiatric and Motor Symptoms
Neurol 94:e1213-e1218, Lima, J.E.E.,et al, 2020

Complex Ataxia
Neurol 95:136-141, Abkur, T.,et al, 2020

GGC Repeat Expansion of NOTCH2NLC in Adult Patients with Leukoencephalopathy
Ann Neurol 86:962-968,809, Okubo, M.,et al, 2019

When MRI is a Clue in Episodic Ataxia
Neurol 93:e2074-e2075, Dhawan, S.R.,et al, 2019

Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
Neurol 92:101-103, Kang, M.J.,et al, 2019

Leg Weakness and Stiffness at the Emergency Room
Neurol 92:e622-e625, af Edholm, K.,et al, 2019

A 54-year-old man with Dyspnea and Muscle Weakness
Neurol 92:e1136-e1140, Chertcoff, A.,et al, 2019

Strokelike Episodes in a Patient with Chronic Gait Abnormalities
JAMA Neurol 76:621-622, Santoro, J.D. & Chitnis, T., 2019

Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement
AJNR 40:903-907, Hartin, I.,et al, 2019

Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019

An Unusual Fundus Finding in a Teenage Girl
JAMA Neurol 75:1566-1567, Filho, F.M.R.,et al, 2018

FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance
Mol Genet Metab 125:281-291, Almannai, M.,et al, 2018

Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss
Neurol 90:e625-e631, Set, K.K.,et al, 2018

A Curable Myopathy Manifesting as Exercixe Intolerance and Respirtory Failure
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Huntington Disease: Clinical Features and Diagnosis
UptoDate Dec 2017, Oksana Suchowersky, 2017

A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
Neurol 89:e220-e223, Xiao, F. & Wang, X.F., 2017

Sudden-Onset Pulsatile Headache in a Previously Healthy Young Man
Neurol 88:e26-e29, Qin, C.,et al, 2017

Gradually Progressive Spastic Ataxia in a Young Man Steadily Unsteady
JAMA Neurol 74:238-241, Dubey, D.,et al, 2017

A 13-year-old boy with Chronic Ataxia and Developmental Delay
Neurol 88:e116-e121, Libdeh, A.A.,et al, 2017

Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
NEJM 376:1668-1678, CASE 13-2017, 2017

A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis
JAMA Neurol 74:733-736, Kung, N.H.,et al, 2017

Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
Front Neurol doi:10.3389/fneur.2017.00472, Velazquez-Perez, L.C.,et al, 2017

Choreoathetosis, Dystonia, and Myoclonus in 3 Siblings with Autosomal Recessive Spinocerebellar Ataxia Type 16
JAMA Neurol 73:888-890, Kawarai, T.,et al, 2016

Neurological Management of Von Hippel-Lindau Disease
Neurologist 21:73-78, Hodgson, T.S.,et al, 2016

SPG7 Mutations Explain a Significant Proportion of French Canadian Spastic Ataxia Cases
Eur J Hum Genet 24:1016-1021, Choquet,K.,et al, 2016

A 40-year old Woman with Difficulty Going Down Stairs in High-Heeled Shoes
Ann Neurol 77:1-7, Scripko, P.,et al, 2015

A 28-year-old Woman with Lower Extremity Spasticity and Microcytic Anemia
Neurol 85:e11-e14, Bonda, C.,et al, 2015

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Gertsmann-Straussler Schneinker Syndrome
Adams & Victors Principles of Neurology, Chp 33, pg 773, Ropper, A.H.,et al, 2014

Neuronal Intranuclear Inclusion Disease Cases with Leukoencephalopathy Diagnosed via Skin Biopsy
JNNP 85:354-356, Sone, J.,et al, 2014

Cerebral Abnormalities in Adults with Ataxia-Telangiectasia
AJNR 35:119-123, Lin, D.D.M.,et al, 2014

Progressive Neuropsychiatric Symptoms and Motor Impairment
JAMA Neurol 71:794-798, Ghadiri, M.,et al, 2014



Showing articles 0 to 50 of 2698 Next >>