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Differential
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abdominal distention
abducens nerve paralysis
abscess, intracerebral
abscess, intracranial
abscess, perivalvular
absence
acid maltase deficiency
acid maltase deficiency, adult
acrocyanosis
acromicria
acyl CoA dehydrogenase deficiency
Addison's disease
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
adrenomyeloneuropathy
adult-onset leukodystrophy, with neuroaxonal spheroids
advances in neurology
adverse drug reaction
agammaglobulinemia
agoraphobia
Aicardi-Goutieres syndrome
alcohol
Alexanders disease
Alexanders disease, adult onset
algorithm
alpha-fetoprotein
alternating hemiplegia
alternating hemiplegia of childhood
Alzheimer's disease
Alzheimer's disease, preclinical
amniocentesis
amyloid angiopathy, cerebral
amyloid beta protein
amyloidosis
amyloidosis, oculoleptomeningeal, familial
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, misdiagnosis
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
angiitis
angiitis, granulomatous of CNS
angiitis, isolated of CNS
angiography, cerebral
angioid streaks
anterior horn cell disease
antibiotic prophylaxis
anticonvulsants
anticonvulsants, discontinuation in seizure-free epileptics
anticonvulsants, selection of
anxiety
aortic valve, bicuspid
aortic valve, lesion of
aphasia
aphasia, progressive, primary
apraxia of eye movements
arachnodactyly
areflexia
arm weakness
arrhythmia, cardiac
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
arteritis, temporal
aspiration
asymptomatic
asystole
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, truncal
ataxic gait
athetosis
atrial myxoma
attention deficit disorder with hyperactivity
atypical
autonomic dysfunction
axonal spheroid
Babinski sign
bacterial endocarditis, neurologic manifestations of
bacterial infection
bacterial infection, CNS
basal ganglia, calcification of
basal ganglia, infarction
basal ganglia, lesion of
behavior, combative
behavioral disorder
benign essential tremor
benign familial nocturnal alternating hemiplegia of childhood
beta adrenergic blocker
biologic markers
biopterin deficiency
bitemporal visual field defect
blepharospasm
blindness
blood dyscrasias, neurologic findings with
bone marrow transplantation
botulinum toxin
brachial plexus
brachial plexus neuropathy
bradycardia
bradykinesia
brain atrophy
brain biopsy
brainstem, infarction of
brainstem, lesion of
brainstem, neoplasms of
brucellosis
brucellosis, nervous system involvement with
bruising
bulbar palsy
cachexia
CAG repeats
calcification, intracranial
calcifications, intracranial, punctate
calf hypertrophy
cane
carbamazepine
carcinoembryonic antigen
carcinoma
carcinoma of pancreas
cardiac surgery
cardiomegaly
cardiomyopathy
caries
carotid angiogram
carotid artery occlusion, bilateral
CAT scan
CAT scan, abnormal
CAT scan, angiography
CAT scan, emission
CAT scan, emission, abnormal
CAT scan, false negative
CAT scan, serial
cataracts
cauda equina
cauda equina, lesion of
cavernous hemangioma
cavernous sinus
cavernous sinus, lesion of
central nervous system, infection of
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar infarction
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 embolism
cerebral infarction
cerebral infarction, small, deep
cerebral infarction, subcortical
cerebral ischemia
cerebral palsy
cerebral venous thrombosis
cerebritis
cerebroretinal vasculopathy
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, biochemical markers of CNS disease
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, red cells in
cerebrospinal fluid, xanthochromia of
cerebrotendinous xanthomatosis
cerebrovascular accident
cerebrovascular accident, cardiac disease causing
cerebrovascular accident, familial occurrence
cerebrovascular accident, infancy and childhood
cerebrovascular accident, mimics
cerebrovascular accident, multiple
cerebrovascular accident, non atherosclerotic cause of
cerebrovascular accident, nonvascular territory
cerebrovascular accident, recurrent
cerebrovascular accident, young adult
cerebrovascular disease
ceruloplasmin, serum
Charcot-Marie-Tooth
cherry red spot-myoclonus syndrome
chilbran skin lesions
children
cholestanol
chorea
choreoathetosis
chromosomal abnormality
chromosome 1
chromosome 11
chromosome 14
chromosome 15
chromosome 17
chromosome 19
chronic progressive external ophthalmoplegia
cigarette smoking
cirrhosis
Clinical Pathologic Conference(C.P.C.)
clonazepam
clubbing of fingers
coagulopathy
cognition
cogwheel rigidty
collagen vascular disease
coloboma
coma
complications
compression neuropathy
compression neuropathy, recurrent
confusion
congenital heart disease
congenital malformation
congenital malformation, non CNS
congestive heart failure
consanguinity
controversies in neurology
copper metabolism, abnormal
corpus callosum
corpus callosum, lesion of
corpus callosum, thinning
cortical blindness
cortical blindness, transient
cost effectiveness
cranial nerve enlargement
cranial nerves
cranial neuropathy
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
cry, abnormal
cry, weak
crying, pathologic
cultured skin fibroblasts
cyclic vomiting
DARS
D-dimer
deafness
deep gray nuclei
degenerative diseases of CNS
Dejerine-Sottas syndrome
delay in diagnosis
delusion
dementia
dementia, age at onset
dementia, cerebrovascular disease causing
dementia, childhood
dementia, familial
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
dementia, subcortical
demyelinating disease
dental procedure, neurologic complications with
dentate nuclei, lesion of
dentatorubral-pallidoluysian atrophy
depression
developmental milestones, loss of
developmental retardation
diabetes mellitus
diagnostic criteria
diaphragmatic paralysis
diarrhea
diet
differential diagnosis
difficulty climbing stairs
dilated aortic root
diplopia
disinhibition-dementia-parkinsonism-amyotrophic complex
distal muscle atrophy
distal muscle weakness
diurnal variation
dizziness
dopa responsive dystonia
dopamine agonist
drooling
dropped head syndrome
drug induced neurologic disorders
dying
dysarthria
dysarthria-clumsy hand syndrome
dysdiadochokinesia
dysmorphic
dysphagia
dyspnea
dystonia
dystonia musculorum deformens
dystonia, children
dystonia, classification
dystonia, etiology of
dystonia, evaluation of
dystonia, face
dystonia, focal
dystonia, painful
dystonia, treatment of
dystrophin
dystrophin associated proteins
DYT1 mutation
ear, pain in
ears of the Lynx MR sign
eating disorder
echocardiogram
echocardiogram, transesophageal, false negative
echocardiogram, transthoracic
echocardiogram, transthoracic, false negative
Ehlers-Danlos syndrome
Ehlers-Danlos syndrome, classification
electrocardiogram, abnormal
electroencephalogram
electroencephalogram, abnormalities of
electroencephalogram, video monitoring with
electromyogram
electron microscopy
electroretinograph
ELISA
embolism, air
embolism, paradoxical
embolism, septic
embolization, therapeutic
emotional lability
encephalopathy
encephalopathy, anoxic
encephalopathy, metabolic
encephalopathy, neonatal
encephalopathy, progressive
endocarditis
endocarditis, acute bacterial
endovascular therapy
enzyme treatment
enzyme, defect
epidemiology of neurology
epileptic encephalopathy
epistaxis
epistaxis, recurrent
esophageal varices
exercise
exercise intolerance
exome sequencing
extraocular muscle lesion
eye movement, disorders of
eye, pain in
Fabry's disease
facial appearance, abnormal
facial nerve palsy
facial weakness
facial weakness, bilateral
factor VII, deficiency
failure to thrive
falling
false negative
familial
familial rectal pain
FARS2 deficiency
fasciculation
fatigue
fatty acid, elevated plasma content
feeding disorder
fever
fibrillations
fibromuscular dysplasia
fine motor function, impaired
fingers, abnormal
fistula, arterio-venous
fistula, arterio-venous, carotid-cavernous
fistula, arterio-venous, dural
fistula, arterio-venous, pulmonary
fluency
flunarizine
flushing
foot drop
Friedreich's ataxia
Friedreich's ataxia, late onset
frontotemporal dementia, behavioral variant
fundus, abnormality of
funduscopic exam
gabapentin
gait disorder
gastrointestinal bleeding
gastrointestinal disease, neurologic complications
gastrointestinal motility
gastrointestinal perforation
gastroparesis
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gender
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
gests antagoniste
GLUT1
GLUT1 deficiency syndrome
glycogen storage disease
Gowers maneuver
gram negative rod
granular osmiphilic material
granulomatosis with polyangiitis
growth hormone deficiency
growth retardation
gynecomastia
hallucination
hand flapping
head lag
head nodding
headache
headache, persistent
headache, positional
headache, severe
headache, throbbing
headache, unilateral
hearing loss
hearing loss, bilateral
hearing problems in children
heart murmur
heart valve surgery
hemangioblastoma
hematuria, gross
hematuria, microscopic
hemianopia
hemianopia, transient
hemiparesis
hemiparesis, transient
hemiplegia
hemoglobin abnormality, neurologic complications of
hemoptysis
hemorrhage, putamenal
hemorrhage, thalamic
hemorrhagic diathesis
hemosiderosis of CNS, superficial
hepatic encephalopathy
hepatic failure
hepatolenticular degeneration(Wilson's disease)
hepatomegaly
hepatosplenomegaly
heralding manifestation
hereditary hemorrhagic telangiectasia(HHT)
herpes simplex encephalitis
herpes simplex encephalitis, differential diagnosis of
hippocampus
homocystinuria
hormone replacement
Horner's syndrome
human immunodeficiency virus type 1
human T-lymphotropic virus type I(HTLV-I)
Huntington's chorea
Huntington's chorea, late onset
Huntington's chorea, misdiagnosis of
Huntington's chorea, sporadic form
hyperactivity
hyperhomocysteinemia
hyperphagia
hyperpigmentation of skin
hyperpyrexia, CNS disorder causing
hyperreflexia
hypertension
hypertonia
hypoglycorrhachia
hypogonadism
hypopigmentation of skin
hyporeflexia
hypotonia
hypotonia, infants
hypoxia
hypoxia, newborn
hypoxic encephalopathy
iatrogenic neurologic disorders
imbalance
immunodeficiency
immunosuppression
impulsivity
inborn errors of metabolism
incoordination
infection
inflexibility, mental
intellectual deficit
intellectual deterioration
interferon alpha
interobserver agreement
intestinal pseudoobstruction
intracerebral hemorrhage
intracerebral hemorrhage, familial
intracerebral hemorrhage, young adult
intracranial hemorrhage
intrauterine
intrinsic hand muscles, wasting of
iron, brain
iron, serum
irritability
ischemic exercise test
islet cell tumor
jaw closure weakness
Jervell Lange-Neilson syndrome
joint hypermobility
juvenile myoclonus epilepsy
Kayser-Fleischer ring
Kearns-Sayre syndrome
ketogenic diet
Kluver-Bucy syndrome
lactate
lactic acidemia
lacunar infarction
Lafora's disease
laughing, pathologic
L-dopa
learning disability
learning disability, in children
Leber's congenital amaurosis
Leber's hereditary optic neuropathy
leg atrophy
leg spasms
leg spasms, painful
lens, dislocation of
leukemia
leukodystrophy
leukoencephalopathy
leukoencephalopathy, adult onset, sporadic
leukoencephalopathy, differential diagnosis
Lewy body
Lewy body disease, diffuse
lifestyle modification
lipid storage disorder of CNS
liver disease
liver function enzymes
lobar atrophy
long QT syndrome
Lorenzo's oil
low back pain
lumbar puncture
lymphoma
malaise
malformation, vascular
malformation, vascular, cerebral
malformation, vascular, familial
malformation, vascular, screening for
mania
manic-depressive
Marfan syndrome
masked facies
masseter muscle weakness
McArdle's disease
MELAS syndrome
memory, impairment of
meningeal enhancement
meningitis, brucellosis
meningitis, CSF cell count-normal
mental retardation
mental status, abnormal
MERRF syndrome
metabolic disorder, primary
metoprolol
microangiopathy, brain
microcephaly
microhemorrhage, intracerebral
migraine
migraine with aura
migraine, hemiplegic
mimics
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
mitral valve prolapse
MNGIE syndrome
molecular genetics
molybdenum cofactor deficiency
monomelic amyotrophy
mononeuropathy
mononeuropathy multiplex
mortality
motor neuron disease
movement disorder
movement disorder, drug induced
movement disorder, extrapyramidal
movement disorder, treatment of
moyamoya
MRI
MRI pattern
MRI, abnormal
MRI, angiography
MRI, contrast enhanced
MRI, cranial nerves
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, false negative
MRI, muscle
MRI, negative
MRI, ring sign
MRI, serial
MRI, spinal cord
MRI, spine
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, familial
multiple sclerosis, misdiagnosis
multiple system atrophy
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle hypertrophy
muscle pain
muscle phosphorylase deficiency
muscle stiffness
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, cardiovascular changes with
muscular dystrophy, central nervous system abnormality
muscular dystrophy, Duchenne
muscular dystrophy, dystrophin normal
muscular dystrophy, limb-girdle
mutism
myasthenia gravis
myasthenia gravis, congenital
myasthenia gravis, differential diagnosis
myasthenia gravis, misdiagnosis of
myasthenia gravis, seronegative
myasthenia gravis, treatment of
myelitis, longitudinal
myelomalacia
myelopathy
myelopathy, chronic progressive
myocardial abscess
myoclonic jerks
myoclonus
myoclonus, epilepsy
myoglobinuria
myopathy
myopathy, genetic
myopathy, metabolic
myopathy, mitochondrial
myopathy, vacuolar
myotonic discharges
nausea and vomiting
neck pain
negative
neoplasm, primary of CNS
neoplasm, primary of CNS-familial occurrence
nerve conduction studies
nerve hypertrophy
nerve root enhancement
nerve root hypertrophy
neuroaxonal leukodystrophy
neurocutaneous disease
neuroendocrinology
neurofibromatosis 1
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic examination, focal
neurologic history
neurologic signs
neurologic symptoms
neuromuscular blockade
neuromuscular disease, electrodiagnosis of
neuromuscular junction, abnormality of
neuronal ceroid-lipofuscinosis
neuronopathy
neuroophthalmology
neuropathology
neuropathy
neuropathy, hereditary peripheral
neuropathy, hypertrophic
neuropathy, vasculitic, systemic
next-generation sequencing
Niemann-Pick disease
normal
nose, abnormal
Notch3 gene
obesity
obsessive-compulsive disorder
occipital lobe, infarction
occipital lobe, lesion of
ocular motility, disorders of
old age, neurology of
ophthalmoplegia
ophthalmoplegia, progressive external
opiate
optic atrophy
optic nerve, lesion of
optic neuropathy
optic neuropathy, bilateral
optic neuropathy, hereditary
optokinetic nystagmus, abnormal
organ rupture
orthopnea
osteogenesis imperfecta
pain
pain, abdominal
pain, anal
pain, back
pain, flank
pain, head
pain, increased response
palatal myoclonus
palliative care
pallido-ponto-nigral degeneration
panic attacks
papilledema
paraparesis
paraparesis, familial spastic
paraparesis, familial spastic, classification
paraparesis, spastic
paraparesis, spastic, tropical
paraplegia
paraspinal muscle
paresthesias
Parkinson disease
Parkinson disease, arteriosclerotic
Parkinson disease, diagnosis
Parkinson disease, differential diagnosis of
Parkinson disease, drug induced
Parkinson disease, juvenile
Parkinson disease, misdiagnosis
Parkinsonism multiple-system atrophy
Parkinsonism syndrome
paroxysmal extreme pain disorder
paroxysmal neurologic deficits
PAS positive
PAS positive material in the brain
pathology
patient information and support
penicillamine
peroxisomal disease
perseveration
personality change
phenylketonuria
phenylketonuria, adult onset
pheochromocytoma
phosphorylase b kinase deficiency
pleocytosis of cerebrospinal fluid
pneumonia
pneumothorax
polycystic kidneys
polycythemia, primary
polymerase chain reaction
polyneuropathy, chronic inflammatory demyelinating
Pompe's disease of glycogen storage
portal caval shunt
posterior cerebral artery territory infarction
postural abnormality
Prader-Labhart-Willi syndrome
pramipexole
precipitating factors
preclinical
pregnancy, neurologic complications in
prenatal
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
primary lateral sclerosis
progeria
prognosis
progressive myoclonic epilepsy
progressive neurologic disorder
progressive subcortical gliosis
progressive supranuclear palsy
proprioception, abnormal
proptosis
prostigmine
protein C deficiency
protein S deficiency
proteinuria
pseudobulbar palsy
pseudomyasthenia
pseudotumor
pseudoxanthoma elasticum
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
psychosis, acute
psychosocial aspects
ptosis
pulmonary embolism
pyramidal tract
pyramidal tract dysfunction
quadriparesis
quadriplegia
radiation hypersensitivity
radiation therapy, stereotactic
ragged-red fibers
rapidly progressing neurologic illness
Red flags
release phenomena
renal cell carcinoma
renal cyst
renal failure
renal infarct
respiratory failure
restless leg syndrome
retina, abnormal
retinal hemangioma
retinal hemorrhages
retinal lesion
retinal tumor
retinopathy
reversible neurologic disorder
review article
riboflavin
rigidity
risk factors
risk factors, modification
risk-benefit assessment
Rosenthal fibers
sarcoglycan
Saudi Arabia
Schilder's disease
schizophrenia
screaming
screening
second wind phenomena
seizure
seizure, cardiac arrhythmia causing
seizure, children
seizure, diagnosis of
seizure, differential diagnosis of
seizure, familial
seizure, intractable
seizure, neonatal
seizure, nonepileptic
seizure, paradoxical
seizure, prognosis in adults
seizure, psychomotor-temporal lobe
seizure, stimulus sensitive
seizure, treatment of
sensorineural hearing loss
sensory loss
sensory polyneuropathy
sensory tricks
seronegative
shaking
short stature
sibling
sickle cell disease
sinemet
single photon emission computed tomography
skin, biopsy
skin, darkening of
skin, hyperextensible
skin, lesions in neurologic disorders
skin, thin
skin, translucent
skull x-ray, abnormal
small vessel disease
sodium channel dysfunction
sodium valproate
spastic ataxia
spastic diplegia
spastic paraplegia, type 11
spasticity
speech disorder
speech disorder, childhood
speech, delayed development of
speech, loss of
spinal cord
spinal cord, compression of
spinal cord, lesion of
spinal cord, neoplasm
spinal cord, vascular malformation of
spinal muscular atrophy
splenomegaly
spontaneous remission
staphylococcus aureus
stare
startle reaction
stereotyped behavior
steroid
steroid therapy, CNS treatment and complications with
stimulation, deep brain
strabismus
streptococcal infection
streptococcus viridans
stridor
strokelike episodes
subarachnoid hemorrhage
subarachnoid hemorrhage, familial
subarachnoid hemorrhage, prognosis
subarachnoid hemorrhage, recurrent
subdural hematoma
suck, poor
sudden death
superior sagittal sinus thrombosis
symmetric brain lesions
syncope
syncope, triggers of
systemic illness
tardive dystonia
telangiectases
telangiectases, retinal
temper tantrums
temporal artery, biopsy
temporal lobe, lesion
temporal lobe, lesion, bilateral
testicular atrophy
tetrahydrobiopterin
thrombocytopenia
thrombophlebitis
toe walking
tomaculous neuropathy
tongue, enlarged
tongue, fasciculations of
tongue, impaired movements of
tongue, protrusion of
tongue, weakness
torsades de points
torticollis
transient ischemic attack
transient ischemic attack, recurrent
transient neurologic deficit
trauma
treatment of neurologic disorder
tremor
tremor, postural
tremulousness
trigeminal nerve
trigeminal nerve, hypertrophy
trinucleotide repeats
tripping
tuberous sclerosis
twins
undiagnosed
Unverricht-Lundborg disease
upgaze, paralysis of
uric acid, low
urinary incontinence
urine, dark
vasculitides
vasculopathy
ventricular tachycardia
very long chain fatty acids
vibratory sensation, abnormal
vision, failure of in childhood
visual acuity, decreased
visual field defect
visual loss
visual loss, congenital
visual loss, slow
vital capacity
Von Hippel Lindau
walking, difficulty with
weakness
weakness, fatiguable
weakness, generalized
weakness, progressive
weaning from respirator, failure to
weight loss
wheelchair
white matter disease
white matter disease, subcortical
wide based gait
word-finding difficulty
workup
wound healing, poor
X-linked bulbospinal neuronopathy
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Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
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Adult Patient Presenting with Spine Pain Following a Motor Vehicle Accident
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A 48-Year-Old Man With Spasticity and Progressive Ataxia
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Ehlers-Danlos Syndromes
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Congenital Myasthenic Syndromes in Adult Neurology Clinic
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Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
NEJM 376:1668-1678, CASE 13-2017, 2017

DARS-Associated Leukoencephalopathy can Mimic a Steroid-Responsive Neuroinflammatory Disorder
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Corticosteroid-Induced Paraplegia - A Diagnostic Clue for Spinal Dural Arterial Venous Fistula
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Non-Alzheimers Dementia 1 Frontotemporal Dementia
Lancet 386:1672-1682, Bang, Jee.,et al, 2015

Molybdenum Cofactor Deficiency
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Degenerative Diseases of the Nervous System, Kennedy Syndrome (X-Linked Bulbospinal Muscular Atrophy)
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Vertebral Artery Dissection in Patients with Autosomal Dominant Polycystic Kidney Disease
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Treat Alzheimer Disease Before It Is Symptomatic
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Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
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Optimal Screening Strategy for Familial Intracranial Aneurysms: A Cost-Effectiveness Analysis
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Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
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Clinicopath Conf, Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL)
NEJM 360:1656-1665, Case 12-2009, 2009

Screening for Intracranial Aneurysms in ADPKD: A More Accurate Risk Assignment Model Is Needed
BMJ 339:706-707, Ong,A., 2009

Aicardi-Gouti�res Syndrome
Br Med Bull 89:183-201, Orcesi, S.,et al, 2009

Two Sets of Identical Twins with Cervical Artery Dissection Concordant for Temporal Artery Pathology
Neurol 71:1035-1037, V�lker,W.,et al, 2008

Seizures on Hearing the Alarm Clock
Lancet 370:2172, Vollmar,C.,et al, 2007

Wilson Disease: Description of 282 Patients Evaluated Over 3 Decades
Medicine 86:112-121, Taly,A.B., et al, 2007

Amyotrophic Lateral Sclerosis
Lancet 369:2031-2041, Mitchell,J.D. & Borasio,G.D., 2007

Paroxysmal Extreme Pain Disorder (Previously Familial Rectal Pain Syndrome)
Neurol 69:586-595, Fertleman,C.R.,et al, 2007

Angelman Syndrome Revisited
Neurologist 13:305-312, Paprocka,J.,et al, 2007

Clinicopath Conf, Dopamine-Responsive-Dystonia Caused by a Mutation in the GCH1 Gene
NEJM 355:831-839, Case 26-2006, 2006

Dystonia
NEJM 355:818-829, Tarsy,D. &Simon,D.K., 2006

Common Misdiagnosis of a Common Neurological Disorder: How Are We Misdiagnosing Essential Tremor?
Arch Neurol 63:1100-1104, Jain,S.,et al, 2006

Restless Legs Syndrome: Is Treatable But Under-Recognised
BMJ 333:457-458, Medcalf,P. &Bhatia,K.P., 2006

Familial Cervical Artery Dissections: Clinical, Morphologic, and Genetic Studies
Stroke 37:2924-2929, Martin,J.J.,et al, 2006

Metabolic Disease and Stroke: MELAS
emedicine.com, Mandava,P.,et al, 2006

Dopamine-Responsive Dystonia
eMedicine (Apr), Nikhar,N.K., 2006

Adrenoleukodystrophy
JAMA 294:3131-3134, Moser,H.W.,et al, 2005

Psychosocial Impact of Screening for Intracranial Aneurysms in Relatives with Familial Subarachnoid Hemorrhage
Stroke 36:836-840, Wermer,M.J.H.,et al, 2005

Migraine and Cerebral White Matter Lesions
The Neurologist 11:19-29, Gladstone,J.P. &Dodick,D.W., 2005



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