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Differential
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abdominal protrusion
abortion, spontaneous
acanthocytosis
agenesis of aqueduct of Sylvius
alpha-fetoprotein
aneurysm
aneurysm, asymptomatic
aneurysm, intracranial
angiography, cerebral
aniridia
anterior tibial muscle weakness
antibodies to voltage-gated calcium channels
apraxia of eye movements
aqueduct of Sylvius, stenosis
aqueductal stenosis
areflexia
arenavirus
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, congenital
ataxia, paroxysmal
ataxia, truncal
ataxic gait
bacterial endocarditis, neurologic manifestations of
Bassen-Kornzweig syndrome
blindness
blood cultures
blue tongue virus
brain biopsy
brainstem, atrophy
brainstem, lesion of
bulbar palsy
bulbar palsy, progressive
calcification, intracranial
calcification, periventricular
calcium channel dysfunction
carcinoembryonic antigen
carcinoma
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
cataracts
cataracts, congenital
central core disease
central nervous system, infection of
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar ataxia, primary
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar hypoplasia
cerebellar infarction
cerebellar lesion
cerebellar vermis
cerebral cortical atrophy
cerebral embolism
cerebral infarction
cerebral infarction, hemorrhagic
cerebral ischemia
cerebral palsy
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, red cells in
cerebrovascular accident
children
chloride channel dysfunction
chorea
choreoathetosis
chorioretinitis
chromosomal abnormality
chromosome 11
Clinical Pathologic Conference(C.P.C.)
Coats syndrome
Cockayne's syndrome
coma
congenital infection, CNS
congenital infection, viral
congenital malformation
congenital myopathy
congenital paresis
consanguinity
cornea, abnormal
cyst
cyst, parenchymal
cyst, porencephalic
cyst, subcortical
Dandy Walker malformation
Dandy Walker malformation, adult
deafmute
deafness
degenerative diseases of CNS
dementia
dental procedure, neurologic complications with
diabetes mellitus
difficulty climbing stairs
drooling
dwarfism
dysarthria
dysphagia
dyspnea
dystonia
electroencephalogram, abnormalities of
electromyogram
electron microscopy
embolism
embolism, septic
embolism, systemic
embryogenesis
encephalitis
encephalitis, viral
encephalopathy
endocarditis
endocarditis, neurologic manifestations with
endocarditis, subacute bacterial
eye movement, disorders of
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
familial
familial hemiplegic migraine
fever
fibrillations
foot deformity
foot drop
Friedreich's ataxia
gait disorder
gait, spastic
gargoylism
gene
gene mutation
genetic linkage
genetic neurologic disorders
Gillespie syndrome
glaucoma
growth retardation
Hallgren's syndrome
hand flapping
head circumference
headache
hearing loss
heart block
hematoma, intracerebral
hepatosplenomegaly
herpes simplex virus
histochemistry of muscle
Hurler's syndrome
hydranencephally
hydrocephalus
hydrocephalus, congenital
hydrocephalus, non-communicating(obstructive)
hydrocephalus, treatment of
hypokalemic periodic paralysis
hypotonia
immunodeficiency
immunohistochemistry
immunosuppression
incoordination
influenza A virus
intellectual deterioration
intracerebral hemorrhage
intrauterine
intrauterine infection
intrauterine infection, viral
intrauterine infection, viral of CNS
iris, abnormal
jittery baby
juvenile paresis
Kearns-Sayre syndrome
keratoconus
Laurence-Moon-Bardet-Biedl syndrome
leukemia
lid closure, weakness of
lymphocytic choriomeningitis
lymphoma
maculopathy
malformation, CNS, congenital
malignant hyperpyrexia
Marinesco-Sjogren syndrome
mental retardation
microcephaly
migraine
migraine, hemiplegic
mimics
misdiagnosis
mitral valve lesion
mitral valve prolapse
mitral valve regurgitation
monoclonal gammopathy
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
mucopolysaccharidoses
multiple system atrophy
mumps virus
muscle biopsy
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, differential diagnosis of
muscular dystrophy, facioscapulohumeral
myasthenic syndrome
mycotic aneurysm
myelomalacia
myeloschisis
myoclonic jerks
myoclonus, epilepsy
myopathy
myopia
myotonia congenita
nausea and vomiting
neck pain
nemaline rod myopathy
nemaline rod myopathy, adult onset
neonatal infection, viral
neuritis
neurocutaneous disease
neuroendocrinology
neurologic disease
neurologic disease, diagnoses of
neurologic signs
neuropathology
neuropathology, brain
neuropathy
nystagmus
obesity
ocular motility, disorders of
ocular myopathy
old age, neurology of
pachygyria
papilledema
paramyotonia congenita
paraspinal muscle
paraspinal muscle weakness
paroxysmal neurologic deficits
parvovirus
pathology
periodic paralysis
personality change
pleocytosis of cerebrospinal fluid
polydactyly
Poretti-Boltshauser syndrome
posterior fossa, lesion of
potassium channel antibodies
potassium channel dysfunction
progeria
prognosis
progressive neurologic disorder
pseudoaneurysm
pseudoretinitis pigmentosa
psychiatric disorder
psychomotor retardation
radiation hypersensitivity
respiratory failure
retinal degeneration
retinitis pigmentosa
retinopathy
review article
rubella encephalitis
rubella encephalitis, progressive
rubella syndrome
rubella virus
rubeola virus
schizophrenia
seizure
serologic testing
serologic testing of cerebrospinal fluid
shunt procedure, ventricular
shunt procedure, ventriculo-peritoneal
skin, lesions in neurologic disorders
sloped shoulders
slow virus infection of CNS
sodium channel dysfunction
spasticity
Spielmeyer Vogt syndrome
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 6
standing difficulty
stem cell transplantation
stooped posture
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
subarachnoid hemorrhage
superior cerebellar artery infarction
sweating
telangiectases
teratogenesis
teratogenesis, viral
thyroiditis
titubation
transplacental virus infections
transverse smile
treatment of neurologic disorder
unconsciousness
urinary incontinence
Usher's syndrome
vasculitides
vertigo
viral infection
viral infection, CNS
viral isolation
virus, slow
visual field defect
visual fields, constricted
walking, difficulty with
weakness
weakness, progressive
weakness, proximal
weight loss
wheelchair
white matter disease
wide based gait
winging of scapula
Showing articles 200 to 250 of 2255 << Previous Next >>

Bilateral Cavernous Carotid Aneurysms: Atypical Presentation of a Rare Cause of Mass Effect
Front Neurol doi:10.3389/fneur.2018.0069, Gagliardi, D.,et al, 2018

Subacute Progressive Ptosis, Ophthalmoplegia, Gait Instability, and Cognitive Changes
JAMA Neurol 75:1284-1285, Lin, J.,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

Pyruvate Dehydrogenase Deficiency (PDCD)
eMedicine.medscape,com, Aug, Frye,R.E.,et al, 2018

Heart Transplantation in a Patient with Myotonic Dystrophy Type 1 and End-Stage Dilated Cardiomyopathy: A Short Term Follow-up
Acta Myologica 37:267-271, Papa, A.A.,et al, 2018

Congenital Asymmetric Crying Facies Syndrome, A Case Report
Medicine 97:31(e11403), Liang,X. & He,B., 2018

Clinical Reasoning: A 49-year-old man with Progressive Numbness, Weakness, and Evidence of Leptomeningeal Enhancement
Neurol 90:e90-e93, Lovett, A.,et al, 2018

The Laser Shoes
Neurol 90:e164-e171, Barthel, C.,et al, 2018

Recurrent Dysarthria and Ataxia in a Young Girl
JAMA Neurol 75:125-126, Romba, 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

Persistent Postural-Perceptual Dizziness (PPPD): A Common, Characteristic and Treatable Cause of Chronic Dizziness
Pract Neurol 18:5-13, Popkirov, S.,et al, 2018

Subacute Paresis in a 28-year-old man with HIV
Neurol 90:432-435, Harada, Y.,et al, 2018

A 52-year-old woman with a 3 weeks of progressive gait ataxia and dysarthria
Neurol 90:e985-e989, Ly, C.,et al, 2018

Long-Term Risk of Hemorrhagic Stroke In Young Patients with Congenital Heart Disease
Stroke 49:1155-1162, Giang, K.W.,et al, 2018

A 60-year-old woman with ataxia
Neurol 90:e1627-e1630, Dandapat, S.,et al, 2018

Disability in adults with arthrogryposis is severe, partly invisible, and varies by genotype
Neurol 90:e1596-e1604, Dai, S.,et al, 2018

Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy
Neurol 90:e1827-e1831, Xiao, F.,et al, 2018

Review of the Neurological Implications of von Hippel-Lindau Disease
JAMA Neurol 75:620-627, Dornbos, D.,et al, 2018

Dyke-Davidoff-Masson syndrome
Neurol 90:e2097-e2098, Durcan, R.,et al, 2018

IgLON5-mediated neurodegeneration is a differential diagnosis of CNS Whipple disease
Neurol 90:1113-1115, Morales-Briceno, H.,et al, 2018

Risk of Ischemic and Hemorrhagic Strokes in Occult and Manifest Cancers
Stroke 49:1585-1592, Andersen, K.K. & Olsen, T.S., 2018

Progressive Weakness and Memory Impairment in a Middle-aged Man
JAMA 320:197-198, DeFilippis, E.M.,et al, 2018

A Curable Myopathy Manifesting as Exercixe Intolerance and Respirtory Failure
Neurol 91:187-190, Silva,A.M.S.,et al, 2018

Isolated Gait Dysfunction Due to Intracranial Hypotension
Neurol 91:271-272, Sasikumar,S.,et al, 2018

Coxa Saltans Misdiagnosed as Functional Gait Disorder
Neurol 91:276-277, Gilbert,D.L.,et al, 2018

A 54-year-old woman with Confusion and Visual Disturbances
Neurol 91:363-367, Rossi, K.C.,et al, 2018

Glutamate Receptor D2 Serum Antibodies in Pediatric Opsoclonus Myoclonus Ataxia Syndrome
Neurol 91:e714-e723, Berridge, G.,et al, 2018

Clnicopathologic Conference Anti-N-Methyl-D-Aspartate (NMDA) Receptor Encephalitis
NEJM 379:870-878, CASE 27-2018, 2018

A Child with Arthrogryposis
Neurol 91:e995-e998, Irumudomom, O. & Ghosh, P.S., 2018

A 58-year-old Woman with Systemic Scleroderma and Progressive Cervical Cord Compression
Neurol 91:e1262-e1264, Karschnia, P.,et al, 2018

Clinical Presentation and Cranial MRI Findings of Listeria Monocytogenes Encephalitis
Neurologist 23:198-203, Arslan, F.,et al, 2018

Congenital Myasthenic Syndromes in Adult Neurology Clinic
Neurol 91:e1770-e1777, Kao, J.C.,et al, 2018

Neuronal Intranuclear Inclusion Disease Showing Intranuclear Inclusions in Renal Biopsy 12 Years Earlier
Neurol 91:884-886, Motoki, M.,et al, 2018

A 35-year-old Woman with Diplopia, Ataxia, and Altered Mental Status
Neurol 91:e1942-e1946, Bauer, Z.,et al, 2018

Pontine Tegmental Cap Dysplasia in a Neonate
Neuol 91:e2100-e2101, Bilgin, N.,et al, 2018

Progressive Gait Difficulty and Incontinence in a 40-year-old Man with HIV
Neurol 91:1065-1070, Silverman, A.,et al, 2018

Neuro-Sweet Disease Presenting as Ischemic Stroke and Aseptic Meningitis
Neurol 91:e2197-e2199, Das, A.S.,et al, 2018

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

Cerebral Atrophy and Leukoencephalopathy in a Young Man Presenting with Encephalitic Episodes
JAMA Neurol 75:1563-1564, Xiao, F.,et al, 2018

Advances in Progressive Supranuclear Palsy: New Diagnostic Criteria, Biomarkers, and Therapeutic Approaches
Lancet Neurol 16:552-563, Boxer, A.L.,et al, 2017

Glial Fibrillary Acidic Protein Immunoglobulin G as Biomarker of Autoimmune Astrocytopathy: Analysis of 102 Patients
Ann Neurol 81:298-309, Flanagan, E.P.,et al, 2017

Huntington Disease: Clinical Features and Diagnosis
UptoDate Dec 2017, Oksana Suchowersky, 2017

Patient with Severe Moyamoya Disease Who Presents with Acute Cortical Blindness
Stroke 48:e126-e129, Sajja, A.,et al, 2017

A Child with Delayed Motor Milestones and Ptosis
Neurol 88:e158-e163, Ghosh, P.S., 2017

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

Clinical Manifestations of the anti-IgLON5 Disease
Neurol 88:1736-1743,1688, Gaig, C.,et al, 2017

Precipitous Deterioration of Motor Function, Cognition, and Behavior
JAMA Neurol 74:591-596, Fernandez-Fournier, M.,et al, 2017

Pregabalin Use Early in Pregnancy and the Risk of Major Congenital Malformations
Neurol 88:2020-2025, Patorno, E.,et al, 2017

Action Tremor, Impaired Balance, and Executive Dysfunction in Midlife
JAMA Neurol 74:603-604, Birch, R.C. & Trollor, J.N., 2017

A 27-year-old man with Acute-Onset Ataxia
Neurol 88:e207-e211, Risco, J. & Weiss, M., 2017



Showing articles 200 to 250 of 2255 << Previous Next >>