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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 250 to 300 of 754 << Previous Next >>

A 72-year-old Man with Rapid Cognitive Decline and Unilateral Muscle Jerks
Neurol 82:e194-e197, Duncan, M.,et al, 2014

Motor Neurone Disease
BMJ 349:g4052, Nageshwaran, S.,et al, 2014

Effect of Rituximab in Patients with Leucine-Rich, Glioma-Inactivated 1 Antibody-Associated Encephalopathy
JAMA Neurol 71:896-900, Irani, S.R.,et al, 2014

A 32-year-old Woman with Right-Sided Numbness and Word-Finding Difficulties
Neurol 83:e98-e102, Busza, A.,et al, 2014

An Unusual Headache
BMJ 349:g5602, Graham, U.M.,et al, 2014

A Cause of Intractable Vomiting
Neurol 83:e141-e144, Yeo, L.L.L.,et al, 2014

A Case of Early-Onset Rapidly Progressive Dementia
JAMA Neurol 71:1445-1449, Cachia, D.,et al, 2014

Primary Sjogren Syndrome Presenting as Isolated Lesion of Medulla Oblongata
Neurol 84:e5-e6, Chen, J.,et al, 2014

Extensive Striatal, Cortical, and White Matter Brain MRI Abnormalities in Wilson Disease
Neurol 81:1557, Trocello, J.M.,et al, 2013

A Welsh-Sparing Dysphasia
Lancet 382: 1608, Rice, S.P.,et al, 2013

Cognitive Delay in a 7-year-old Girl
Neurol 81: e148-e150, Cachia, D. & Stine, C., 2013

Limbic Encephalitis as the Presenting Feature of Sj�gren Syndrome
Neurol Clin Pract 3:165-167, Finelli, P. & Inoa, V., 2013

Brain Abnormalities as an Initial Manifestation of Neuromyelitis Optica Spectrum Disorder
MSJ 17:1107-1112, Kim, W.,et al, 2013

Perfusion imaging of cerebral hyperfusion syndrome following revascularization
Neurol 81:e25-e26, Kalra, V.B.,et al, 2013

Cerebral Hyperperfusion Syndrome: A Novel Presentation of Internal Carotid Artery Dissection
Neurol 81:599-601, Pinho, J.,et al, 2013

Aspergillus Meningitis: A Rare Clinical Manifestation of Central Nervous System Aspergillosis
J Infect 66:218-238, Antinori, S.,et al, 2013

Clinical Reasoning: A 13-year-old Boy Presenting with Dystonia,Myoclonus,and Anxiety
Neurol 78:e72-e76, Blackburn,J.S. and Cirillo,M.L., 2012

Acute Stroke Imaging: What is Sufficient for Triage to Endovascular Therapies?
AJNR 33:790-792, Lev, M.H., 2012

Acute Stroke Imaging: CT with CT Angiography and CT Perfusion before Management Decisions
AJNR 33:792-794, Fox, A.J.,et al, 2012

Clinical Reasoning: A Young Man with Reversible Paralysis, Cerebral White Matter Lesions, and Peripheral Neuropathy
Neurol 79: e70-e72, Zhong, L.,et al, 2012

Clinicopathologic Conference, Acute Ischemic Stroke due to Basilar Artery Embolism. Patent Foramen Ovale
NEJM 367:1450-1460, Case 31-2012, 2012

Evidence-based Guideline: Diagnostic accuracy of CSF 14-3-3 Protein in Sporadic Creutzfeldt-Jakob Disease
Neurol 79:1499-1506, Muayqil, T.,et al, 2012

Differential Diagnosis of Jakob-Creutzfeldt Disease
Arch Neurol 69:1578-1582,1554, Paterson, R.,et al, 2012

Myasthenia Gravis
BMJ 345:e8497, Spillane, J.,et al, 2012

Heterozygous de-Novo Mutations in ATP1A3 in Patients with Alternating Hemiplegia of Childhood:A Whole-Exome Sequencing Gene-Identification Study
Lancet Neurol 11:764-773, Rosewich,H.,et al, 2012

Autoimmune Encephalopathy
Semin Neurol 31:144-157, Flanagan, E.,et al, 2011

Cortical Restricted Diffusion as the Predominant MRI Finding in Sporadic Creutzfeldt-Jakob Disease
Acta Radiologica 52:336-339, Talbott,S.D.,et al, 2011

Rapidly Progressive Corticobasal Degeneration Syndrome
Case Rep Neurol 3:185-190, Herrero Valverde, A.,et al, 2011

Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis
NEJM 364:1062-1074, Case 8-2011, 2011

The Evaluation of Rapidly Progressive Dementia
The Neurologist 17:67-74, Rosenbloom,M.H. &Atri,A., 2011

Multimodal Imaging Does Not Delay Intravenous Thrombolytic Therapy in Acute Stroke
AJNR 32:864-68, Salottolo, K.M.,et al, 2011

Diffusion-weighted MRI hyperintensity patterns differentiate CJD from other rapid dementias
Neurol 76:1711-1719, Vitali, P.,et al, 2011

A Case of Hashimoto Encephalopathy Clinical Manifestation, Imaging, Pathology, Treatment, and Prognosis
The Neurologist 17:141-143, Zhao, W.,et al, 2011

Intravenous Thrombolytic Therapy for Acute Ischemic Stroke
NEJM 364:22, Wechsler, L.R., 2011

Late onset autism and anti-NMDA-receptor encephalitis
Lancet 378:98;378, Creten, C.,et al, 2011

Advanced Brain Imaging Studies Should Be Performed in Patients With Suspected Stroke Presenting Within 4.5 Hours of Symptom Onset
Stroke 42-2666-2667,2670, Parsons, M.W., 2011

Advanced Brain Imaging Studies Should Not Be Performed in Patients With Suspected Stroke Presenting Within 4.5 Hours of Symptom Onset
Stroke 42:2668-2669,2670, Lyden, P.D., 2011

Rapidly Progressive Alzheimer Disease
Arch Neurol 68:1124-1130, Schmidt, C.,et al, 2011

Treatable Neurological Disorders Misdiagnosed as Creutzfeldt-Jakob Disease
Ann Neurol 70:437-444, Chitravas, N.,et al, 2011

Folic Acid Supplements in Pregnancy and Severe Language Delay in Children
JAMA 36:1566-1573, Roth, C.,et al, 2011

A Strange Case of Waitress Headache
Lancet 378:1824, Libera, D.D.,et al, 2011

Acutely Injured Patients on Dabigatran
NEJM 365:2039-2040, Cotton, B.A.,et al, 2011

Cerebral Blood Flow is the Optimal CT Perfusion Parameter for Assessing Infarct Core
Stroke 42:3435-3440, Campbell, B.C.V.,et al, 2011

Clinicopathologic Conference, Thymoma with Paraneoplastic Myasthenia Gravis, Polymyositis and Myocarditis, and Brain Stem Encephalitis
NEJM 365:2413-2422, Case 39-2011, 2011

Genetic Susceptibility to Stuttering
NEJM 362:750-752, Fisher,S.E. &Phil,D., 2010

Clinicopath Conf, Intravascular Large-B-Cell Lympoma
NEJM 362:1129-1138, Case 9-2010, 2010

Functional Contrast-Enhanced CT for Evaluation of Acute Ischemic Stroke Does not Increase the Risk of Contrast-Induced Nephropathy
AJNR 31:817-821, Lima,F.O., et al, 2010

Cost-Effectiveness of Multimodal CT for Evaluation Acute Stroke
Neurol 75:1678-1685, Young,K.C.,et al, 2010

Clinical and Radiological Features of Rotavirus Cerebellitis
AJNR 31:1591-1595, Takanashi,J.,et al, 2010

Profound Deafness in Childhood
NEJM 363:1438-1450, Kral,A.,et al, 2010



Showing articles 250 to 300 of 754 << Previous Next >>