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Differential
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achilles tendon, enlarged
acute ataxia of childhood
acute cerebellar ataxia
agitation
akinetic mute
alcohol intolerance
alcoholism
alternating rapid movement
alternating rapid movement, impaired
ammonia
ANA
anasarca
anemia
angiography, cerebral
ankle edema
anorexia
anti Yo antibody
aphasia
aphonia
areflexia
ascites
ataxia
ataxia telangiectasia
ataxia, acute onset
ataxia, cerebellar
ataxia, progressive
ataxia, sensory
ataxia, truncal
ataxic gait
atypical
autoantibodies
autoimmune encephalopathy
automobile accidents
B 12 deficiency
Babinski sign
bacterial infection
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavior, combative
behavioral disorder
belligerent
biologic markers
blepharospasm
bradykinesia
brain biopsy
brainstem, atrophy
brainstem, lesion of
CAG repeats
carbon monoxide poisoning
carcinoma
carcinoma of breast
cardiomyopathy
CAT scan
CAT scan, angiography
CAT scan, angiography, false negative
CAT scan, perfusion
CAT scan, venography
cataracts
cerebellar ataxia, autosomal recessive
cerebellar ataxia, hereditary
cerebellar ataxia, neuropathy and vestibular areflexia syndrome
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar cognitive affective syndrome
cerebellar degeneration
cerebellar lesion
cerebellitis
cerebellitis, autoimmune
cerebellum, disease of
cerebral cortex
cerebral cortical atrophy
cerebrospinal fluid, oligoclonal IgG in
cerebrovascular accident
cerebrovascular accident, complications with
cerebrovascular accident, location of
cerebrovascular accident, multiple
cerebrovascular accident, silent
ceruloplasmin, serum
choking
chromosomal abnormality
chromosome 17
Clinical Pathologic Conference(C.P.C.)
clonus
cognition
cognition, slowed
coma
complications
confusion
cortical infarction
cough
cranial nerve palsies
cranial neuropathy, multiple
Creutzfeldt-Jakob disease, genetic
crying, pathologic
cystatin C mutation
deep gray nuclei
delay in diagnosis
delirium
delusion
dementia
dementia, familial
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
dementia, thalamic
dementia, transmissible
depression
dexterity, impaired
diabetes mellitus
diarrhea
diet
differential diagnosis
difficulty climbing stairs
diplopia
disability, neurological
disorientation
dizziness
down-beat nystagmus
down-beat nystagmus, primary position of gaze
DPPX
DPPX, antibodies, encephalitis
drooling
dural arteriovenous malformation
dysarthria
dysdiadochokinesia
dysgraphia
dysmetria
dysphagia
dystonia
dystonia, face
dystonia, focal
ear, pain in
echolalia
edema, pedal
EDTA(ehtylenediamine tetraacetic acid)
ejection fraction, abnormal
electroencephalogram, abnormalities of
electroencephalogram, periodic complexes
electromyogram
emotional lability
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalomyelitis, postinfectious
encephalopathy
encephalopathy, delayed
encephalopathy, progressive
Epstein-Barr virus
Erdheim-Chester disease
esophageal varices
euphoria
executive dysfunction
eye movement, disorders of
facial expression abnormality
falling
false negative
familial
fatigue
fever
fine motor function, impaired
finger nose finger test
finger numbness
fistula, arterio-venous, dural
foam cells
food-borne infection
Friedreich's ataxia
frontal lobe, atrophy
gait disorder
gammaglobulin therapy, intravenous
gastric partitioning
gaze palsy, horizontal
gene
gene mutation
genetic neurologic disorders
genetic testing
Gerstmann-Straussler-Scheinker disease
grandiosity
hallucination
hand weakness
hands, fisted
handwriting
head nodding
headache
heel swelling
heel-knee-shin test
hemidystonia
hemorrhage, thalamic
hepatic encephalopathy
hepatic failure
hepatolenticular degeneration(Wilson's disease)
hepatolenticular degeneration(Wilson's disease), presymptomatic
heralding manifestation
hiccoughs
hiccoughs, intractable
histiocytosis
hoarseness
hyperammonemic encephalopathy
hyperesthesia
hyperhomocysteinemia
hyperosmolality
hyperreflexia
hypersomnia
hypoalbuminemia
hypometric saccades
hypotonia
iatrogenic neurologic disorders
imbalance
imbalance, postural
immunohistochemistry
impulsivity
inattention
incarceration
incontinence, fecal
incoordination
infection
infectious mononucleosis
infectious mononucleosis, neurologic findings with
inferior olivary nucleus
insomnia
intellectual deficit
intellectual deterioration
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
Jakob-Creutzfeldt disease, variant
Kayser-Fleischer ring
lactic dehydrogenase(LDH)
lateropulsion
laughing, pathologic
leg swelling
leukoencephalopathy
leukopenia
level of consciousness, decreased
listeria monocytogenes
listeriosis, CNS
liver disease
liver function enzymes
lobar atrophy
logopenia
lumbar puncture, complications of
lymphoma
lymphoma involving CNS
lymphoma, primary of CNS
manganese intoxication
mania
masked facies
medulla oblongata, lesion of
memory, defect of recent
memory, impairment of
meningitis-encephalitis PCR panel
mental status, abnormal
methylmalonic acid, serum
methylmalonic acidemia
micrographia
microhemorrhage, intracerebral
midbrain, atrophy
middle cerebellar peduncle, lesion
misdiagnosis
molecular genetics
mood change
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, angiography
MRI, angiography, false negative
MRI, contrast enhanced
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, false negative
MRI, negative
MRI, punctate pattern
MRI, ring sign
MRI, T1 weighted high signal foci
MRI, venography
multiple sclerosis, differential diagnosis of
multiple sclerosis, misdiagnosis
muscle biopsy
mutism
myelinolysis, extrapontine
myelomalacia
myoclonic jerks
myoclonus
myoclonus, stimulus sensitive
nausea and vomiting
neck pain
neoplastic angioendotheliosis
nerve conduction studies
neurologic disease, diagnoses of
neurologic signs
neuronopathy, sensory
neuropathology
neuropathy
neuropathy, sensory
next-generation sequencing
nutritional deficiency
nystagmus
olivary degeneration, hypertrophic
ophthalmoplegia, progressive external
optic atrophy
osmotic demyelination syndrome
otitis, neurologic complications with
palatal myoclonus
paraneoplastic cerebellar degeneration
paranoia
paraphasias
paresthesias
paresthesias, hands
Parkinson disease
Parkinson disease, L-dopa nonresponsive
Parkinsonism syndrome
pathologic reflex
penicillamine
pernicious anemia
personality change
pleocytosis of cerebrospinal fluid
POLG1 gene
polymerase chain reaction
pons, lesion of
positional head-hanging test
post infectious cerebellar ataxia
postinfectious
postural abnormality
pregnancy, neurologic complications in
prion disease
prion protein gene
prisoner
prognosis
progressive ataxia and palatal tremor
progressive neurologic disorder
protein 14-3-3, cerebrospinal fluid
pseudobulbar palsy
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
psychotic behavior
ptosis
ptosis, bilateral
pull test
pursuit eye movements, abnormal
RAPID CT perfusion maps
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
reading disorder, acquired
real-time quaking-induced conversion
rehabilitation for neurologic disorders
release phenomena
remote effect of cancer on the nervous system
renal stones
retropulsion
reversible neurologic disorder
review article
rigidity
Romberg's sign
saccadic eye movements, abnormal
seizure
sleep pathology and physiology
slit lamp examination
slurred speech
spasticity
speech disorder
speech disorder, non aphasic
speech, loss of
speech, pressured
speech, slowed
spinocerebellar ataxia
spinocerebellar ataxia type 7
splenomegaly
spongy degeneration of brain
spontaneous remission
square wave jerks
staggering
startle myoclonus
startle reaction
suicide
swallow evaluation
symmetric brain lesions
systemic illness
tandem gait, ataxic
tangential
tau protein
tauopathy
thalamus, lesion of
thalamus, lesion of-bilateral
thrombocytopenia
titubation
tongue, numbness of
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, intention
trientine dihydrochloride
trinucleotide repeats
upgaze, paralysis of
urinary incontinence
venous hypertension
venous ischemia
vertigo
vestibulopathy
vibratory sensation, abnormal
viral infection
viral infection, CNS
vision, blurred
visual acuity, decreased
vitamin E deficiency
voice, abnormality of
walking frame
walking, difficulty with
weight loss
welder
wheelchair
white matter disease
wide based gait
work loss
workup
writing
zinc
Showing articles 150 to 200 of 754 << Previous Next >>

Facial Myokymia and Myorhythmia in Anti-IgLON5 Disease
Neurol 91:e1659, Vetter, E.,et al, 2018

Pantothenate Kinase - Associated Neurodegeneration (PKAN)
Emedicine.Medscape Sept, Hanna, P.A. & Benbadis, S.R., 2018

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

Rapid Progression of Reversible Cognitive Impairment in an 80-year-old Man
Neurol 91:1109-1113, Bouthour, W.,et al, 2018

Clinicopathological Conference, Insulinoma
NEJM 379:376-384, Case 23-2018, 2018

Use of Imaging to Select Patients for Late Window Endovascular Therapy
Stroke 49:2256-2260, Albers, G.W., 2018

Atypical Parkinsonian Syndromes: A General Neurologists Perspective
Eur J Neurol 25:41-58, Deutschlander, A.B.,et al, 2018

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

Young Adult with Dysphagia and Severe Weight Loss
Neurol 91:e1083-e1086, Irumudomon, O. & Ghosh, P.S., 2018

Endovascular Stroke Therapy in the Late Time Window
Stroke 49:2559-2561, Schellinger, P.D. & Demaerschalk, B.M., 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

Thrombectomy 6 to 24 Hours after Stroke with a Mismatch between Deficit and Infarct
NEJM 378:11-22,81, Nogueira, R.G.,et al, 2018

Recurrent Dysarthria and Ataxia in a Young Girl
JAMA Neurol 75:125-126, Romba, M.,et al, 2018

Enlightenment and Challenges Offered by DAWN Trial (DWI or CTP Assessment with Clinical Mismatch in the Triage of Wake Up and Late Presenting Strokes Undergoing Neurointervention with Trevo)
Stroke 49:498-500, Saposnik, G.,et al, 2018

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

Thrombectomy for Stroke at 6 to 16 Hours with Selection by Perfusion Imaging
NEJM 378:708-718, Albers, G.W.,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

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

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

An unusual neuropsychiatric manifestation of systemic lupus erythematosus
Neurol 90:e1929-e1932, Dongkyung, D.,et al, 2018

Magnetic Resonance Imaging Selection for Endovascular Stroke Therapy
Stroke 49:1402-1406, Simonsen, C.Z.,et al, 2018

Clinical Pathologic Conference, West Nile Virus Encephalitis
NEJM 377:1878-1886, Case 34-2017, 2017

Clinical Imaging Factors Associated with Infarct Progression in Patients with Ischemic Stroke During Transfer for Mechanical Thrombectomy
JAMA Neurol 74:1361-1367,1298, Boulouis, G.,et al, 2017

Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
NEJM 377:2376-2385, Case 38-2017, 2017

Diagnosis and Management of Dementia with Lewy Bodies
Neurol 89:88-100, McKeith, I.G.,et al, 2017

A 54-year-old woman with Dementia, Myoclonus, and Ataxia
Neurol 89:e7-e12, Ali, F.,et al, 2017

Migraine
NEJM 377:553-561, Charles, A., 2017

Cerebral Amyloid Angiopathy-Related Inflammation Presenting with Isolated Leptomeningitis
Neurol 89:e66-e67, Kang, P.,et al, 2017

DAWN: Thrombectomy Effective Up to 24 Hours after Stroke
Medscape May, Hughes, S., 2017

Computed Tomographic Perfusion to Predict Response to Recanalization in Ischemic Stroke
Ann Neurol 81:849-856, Lansberg, M.G.,et al, 2017

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

Intracranial Dural Arteriovenous Fistulae
Stroke 48:1424-1431, Reynolds, M.R.,et al, 2017

Primary Angiitis of the Central Nervous System
Stroke 48:1248-1255, Boulouis, G.,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

Man with Recurrent Paralysis and Cerebral White Matter Lesions
JAMA Neurol 74:599-600, Xiao, F., 2017

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

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

Clinicopathologic Conference, Primary Progressive Aphasia, Semantic Variant, due to TAR DNA Binding Protein 43 associated Frontotemporal Lobar Degen
NEJM 376:158-167, Case 1-2017, 2017

Endovascular Treatment for Patients with Acute Stroke Who Have a Large Ischemic Core and Large Mismatch Imaging Profile
JAMA Neurol 74:34-40, Rebello, L.C.,et al, 2017

Clinicopathologic Conference, Posterior Cortical Atrophy with Frontotemporal Lobe Dementia with Gene Mutation
JAMA Neurol 74:114-118, , 2017

Clinicopathologic Conference, Granulomatous Amebic Encephalitis and Sarcoidosis (Inactive)
NEJM 376:368-379, Case 3-2017, 2017

Characteristics in Limbic Encephalitis with Anti-Adenylate Kinase 5 Autoantibodies
Neurol 88:514-524,508, Do, L. & Chanson, E., 2017

Cranial Nerve Hypertrophy in IgG4 Anti-Neurofascin 155 Antibody-Positive Polyneuropathy
Neurol 88:e52, Franques, J.,et al, 2017

Intractable Epilepsy and Progressive Cognitive Decline in a Young Man
JAMA Neurol 74:737-740, Cohen, A.L.,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

Powassan Virus-A New Reemerging Tick-Borne Disease
Front Public Health 5:342, Fatmi,S.S., et al, 2017

Wernekink Commissure Syndrome Secondary to Bilateral Caudal Paramedian Midbrain Infarction Presenting with a Unique "Heart or V" Appearance Sign:Case Report and Review of the Literature
Front Neurol soi.10.3389/fneur.2017.00376,Aug, Zhou,C.,et al, 2017



Showing articles 150 to 200 of 754 << Previous Next >>