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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 100 to 150 of 754 << Previous Next >>

Dural Arteriovenous Fistula Presenting with Reversible Dementia
Ann Neurol 90:512-513, Yoon, J.Y.,et al, 2021

Facial Numbness, Dysarthria, Muscle Atrophy, and Weakness in a Young Patient
JAMA Neurol 78:1273-1274, Liu, Y.,et al, 2021

Sporadic Creutzfeldt-Jakob Disease in a Very Young Person
Neurol 97:813-816,801, Appleby, B.S.,et al, 2021

Automated Brain Perfusion Imaging in Acute Ischemic Stroke: Interpretation Pearls and Pitfalls
Stroke 52:3728-3738, Nicolas-Jilwan, M. & Wintermark, M., 2021

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

A 71-Year-Old Man Presenting with Acute Onset Dysarthria and Dysphagia
Neurol 96:180-184, Spagni, G.,et al, 2021

Which Imaging Approach Should be Used for Stroke of Unknown Time of Onset?
Stroke 52:373-380, Simonsen, C.Z.,et al, 2021

Clinicopathologic conference, Frontotemporal Lobar Degeneration with tau-positive inclusions consistent with Picks disease
NEJM 383:2666-2675, Case 41-2020, 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

A 42-year-old Woman with Progressive Cognitive Difficulties and Gait Imbalance
Neurol 94:e1219-e1226, Slama, M.C.C.,et al, 2020

An 81-year-old Woman with Decreased Consciousness and Fluctuating Right Facial Droop
Neurol 94:843-848, Van Ommeren, R.,et al, 2020

Carotid-Cavernous Fistula Presenting with Bilateral Abducens Palsy
Stroke 51:e107-e110, Peng, T.J.,et al, 2020

Ears of the Lynx Magnetic Resonance Imaging Sign
Ann Neurol 88:16-17, Baghbanian, S.M.,et al, 2020

Tapia Syndrome at the Time of the COVID-19 Pandemic
Neurol 95:312-313, Decavel, P.,et al, 2020

Clinicopathologic Conference, Borrelia Miyamotoi Infection
NEJM 383:1578-1586, Case 32-2020, 2020

Bornavirus Encephalitis Shows a Characteristic Magnetic Resonance Phenotype in Humans
Ann Neurol 88:723-735, Finck, T.,et al, 2020

Dressing Apraxia as Initial Manifestation of Creutzfeldt-Jakob Disease
Tremor and Other Hyperkinetic Movements 10:1-3, Heckmann, J.G.,et al, 2020

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

Intravenous Alteplase for Stroke with Unknown Time of Onset Guided by Advanced Imaging:Systematic Review and Meta-Analysis of Individual Patient Data
Lancet 396:1574-1585, Thomalla,G.,et al, 2020

Multimodal CT or MRI for IV thrombolysis in ischemic stroke with unknown time of onset
Neurol 95:e2954-e2964, Macha, K.,et al, 2020

Clinical features, prognostic factors, and antibody effects in anti-mGluR1 encephalitis
Neurol 95:e3012-e3025, Spatola, M.,et al, 2020

Recent Administration of Iodinated Contrast Renders Core Infarct Estimation Inaccurate Using RAPID Software
AJNR 41:2235-2242, Copelan, A.Z.,et al, 2020

Immunocompetent Patient with Multiple Cranial Nerve Palsies, Ataxia, and Cognitive Decline
Neurol 94:e225-e229, Nigam, M.,et al, 2020

Rapidly Progressive Gait Disorder and Cranial Nerves Involvement in a 9-year-old boy
Neurol 94:e330-e334, Lipp, A.,et al, 2020

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

Palatal Myoclonus, Abnormal Eye Movements, and Olivary Hypertrophy in GAD65-Related Disorder
Neurol 94:273-275, Macaron, G.,et al, 2020

Homonymous Hemianopia with Normal Magnetic Resonance Imaging
JAMA Ophthalmol doi:10.1001/JAMAOphthalmol.2020.0447, Cai, S.,et al, 2020

Functional Neurological Disorder
Stroke 51:1629-1635, Popkirov, S., et al, 2020

A 47-year-old Man with Rapidly Progressive Ataxia and Vitiligo
Neurol 94:e1664-e1669, Han, F.,et al, 2020

Rapid Progression of Prion Disease Associated with Transverse Myelitis
Neurol 94:e1670-e1672, Hussein, O.,et al, 2020

Clinicopathologic Conference, AA Amyloidosis, Complicated by Cerebral Mucormycosis
NEJM 382:1457-1466, Case 11-2020, 2020

Clinicopathologic Conference, Amyotrophic Lateral Sclerosis
NEJM 380:1566-1574, Case 12-2019, 2019

Thrombolysis Guided by Perfusion Imaging up to 9 Hours after Onset of Stroke
NEJM 380:1795-1803,1865, Ma, H.,et al, 2019

Toxic Diffuse Isolated Cerebellar Edema from Over-the-Counter Health Supplements
Neurol 92:965-966, Kim, D.D.,et al, 2019

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

A 47-year-old Man with Diffuse White Matter Disease and Rapidly Progressive Dementia
Neurol 92:e2832-e2837, Di Luca, D.G.,et al, 2019

Extending Thrombolysis to 4.5-9 h and Wake-Up Stroke Using Perfusion Imaging: A Systematic Review and Meta-Analysis of Individual Patient Data
Lancet 394:139-147,97, Campbell, B.C.V.,et al, 2019

A 68-year-old Man with Rapid Cognitive Decline
Neurol 93:315-318, Berth, S.H.,et al, 2019

Childhood Primary Angiitis of the Central Nervous System
www.UptoDate.com, Dec, Twilt, M. & Benseler, S., 2019

Clinicopathologic Conference, Powassan Virus Encephalitis
NEJM 380:380-387, Case 3-2019, 2019

Automated CT Perfusion Imaging for Acute Ischemic Stroke
Neurol 93:888-898, Vagal, A.,et al, 2019

No-Cutoff Large Vessel Occlusion Stroke
Neurol 93;1014-1015, Atchaneeyasakul, K.,et al, 2019

Orofacial Dyskinesia in a Young Man
JAMA Neurol 76:1517-1518, Tian, X.,et al, 2019

Automated ASPECTS in Acute Ischmeic Stroke: A Comparative Analysis with CT Perfusion
AJNR 40:2033-2038, Sundaram, V.K.,et al, 2019

Rapidly Progressive Vision Loss in a Patient with Breast Cancer
JAMA 322:1098-1099, Izzo, M.C.,et al, 2019

Clinicopathologic Conference, Adenovirus Meningoencephalitis
NEJM 381:1459-1470, Case 31-2019, 2019

Central Nervous System Infections Due to Coccidioidomycosis
J Fungi 5:2-12, Jackson, N.R.,et al, 2019

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

Wilson Disease
NIDDK Oct2018, , 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



Showing articles 100 to 150 of 754 << Previous Next >>