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Differential
(Click to cross reference)
acalculia
agnosia
agnosia, visual
agraphia
akinetic mute
alexia
alexia with agraphia
Alzheimer's disease
Alzheimer's disease, visual variant
amyloid angiopathy, cerebral
amyloid angiopathy, cerebral, inflammatory type
amyloid plaques
anemia
aneurysm, intracranial
aneurysm, multiple intracranial
angular gyrus
angular gyrus syndrome
anomic aphasia
aphasia
aphasia, transcortical
aphasia, transcortical-sensory
apolipoprotein E
areflexia
arterial dissection, carotid
arteriopathy
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, truncal
automobile accidents
Balint's syndrome
blacks
bovine spongiform encephalopathy
burning paresthesia
carotid angiogram
carotid artery occlusion, neck
CAT scan
CAT scan, abnormal
CAT scan, angiography
CAT scan, dense artery sign
central nervous system, infection of
cerebellar atrophy, primary
cerebellar degeneration
cerebellar plaques, amyloid
cerebral cortex
cerebral cortical atrophy
cerebral dominance
cerebrovascular accident
cerebrovascular accident, multiple
cerebrovascular accident, thrombolytic agents in treatment
cerebrovascular accident, young adult
Clinical Pathologic Conference(C.P.C.)
confusion
deep gray nuclei
degenerative diseases of CNS
dementia
dementia, differential diagnosis of
dementia, familial
dementia, presenile
dementia, rapidly progressive
dementia, transmissible
depression
dexterity, impaired
diagnostic criteria
dysarthria
dyspraxia
epidemic
epidemiology of neurology
familial
fatal familial insomnia
fibrinolytic agents
finger agnosia
finger naming
gait disorder
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic testing
Gerstmann syndrome
Gerstmann-Straussler-Scheinker disease
headache
headache, severe
hemoglobin abnormality, neurologic complications of
heralding manifestation
Howell-Jolly bodies
hyperbilirubinemia
hyporeflexia
iatrogenic neurologic disorders
immunosuppressive agents
intellectual deterioration
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, variant
jaundice
kuru
lactic dehydrogenase(LDH)
left-right orientation
leukoencephalopathy
lobar atrophy
memory, defect of recent
mental status, abnormal
microhemorrhage, intracerebral
molecular genetics
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, disappearing lesion on
neurofibrillary degeneration
neurologic disease, diagnoses of
neurologic examination, focal
neurologic signs
neuropathology
neuropathology, brain
nystagmus
paresthesias
Parkinson disease
Parkinsonism syndrome
peripheral blood smear, abnormal
perseveration
polymerase chain reaction
posterior cortical atrophy
prion disease
prion protein gene
progressive neurologic disorder
protein 14-3-3, cerebrospinal fluid
psychosis
pursuit eye movements, abnormal
pyramidal tract dysfunction
review article
scrapie
seizure
sickle cell crisis
sickle cell disease
single photon emission computed tomography
spongy degeneration of brain
tandem gait, ataxic
target red cells
thalamus, lesion of
tissue plasminogen activator, intravenous
treatment of neurologic disorder
vasculopathy
virus, slow
visual loss
weight loss
Western immunoblot test
white matter disease
Showing articles 0 to 22 of 22

Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
Neurol 92:101-103, Kang, M.J.,et al, 2019

Clinicopathologic Conference, Cerebral Infarction from Internal Carotid Occlusion Related to Sickle Cell Arteriopathy
NEJM 374:1265-1275, Case 10-2016, 2016

A Case of Subacute Cognitive Decline in a 76-year-old Man
Neurol 87:e124-e128, MacLellan, A.,et al, 2016

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Gertsmann-Straussler Schneinker Syndrome
Adams & Victors Principles of Neurology, Chp 33, pg 773, Ropper, A.H.,et al, 2014

Early Clinical Signs and Imaging Findings in Gerstmann-Straussler-Scheinker Syndrome (Pro102Leu)
Neurol 66:1672-1678, Arata,H.,et al, 2006

Transmissible Spongiform Encephalopathies
Lancet 363:51-61, Collins,S.J.,et al, 2004

Posterior Cortical Atrophy:Neuropathologic Correlations
Arch Neurol 51:269-274, Victoroff,J.,et al, 1994

Human Prion Diseases
Ann Neurol 35:385-395, Prusiner,S.B.&Hsiao,K.K., 1994

Gerstmann-Straussler-Schneinker Syndrome:MR Findings
J Comput Assist Tomogr 17:326-327, Wimberger,D.,et al, 1993

Gerstmann's Syndrome
Arch Neurol 49:445-447, Benton,A.L., 1992

The Spongiform Encephalopathies, Editorial
JNNP 54:761-763, Will,R.G., 1991

Prion Dementia Without Characteristic Pathology
Lancet 336:7-9, 21-221990., Collinge,J.,et al, 1990

Inherited Human Prion Diseases
Neurol 40:1820-1827, Hsiao,K.&Prusiner,S.B., 1990

Diagnosis of Gerstmann-Straussler Syndrome in Familial Dementia with Prion Protein Gene Analysis
Lancet 2:15-17, Collinge,J.,et al, 1989

Gerstmann-Straussler-Scheinker Disease, I, Extending the Clinical Spectrum
Neurol 39:1446-1452, Farlow,M.R.,et al, 1989

Gerstmann-Straussler-Scheinker Disease, II, Neurofibrillary Tangles & Plaques with PrP-amyloid in an Affected Family
Neurol 39:1453-1461, Ghetti,B.,et al, 1989

Posterior Cortical Atrophy
Arch Neurol 45:789-793, Benson,D.F.,et al, 1988

Prions & Neurodegenerative Diseases
NEJM 317:1571-1581, 15971987., Prusiner,S.B., 1987

Diagnosis of Creutzfeldt-Jakob Disease by Western Blot Identification of Marker Protein in Human Brain Tissue
NEJM 314:547-551, Brown,P.,et al, 1986

Gerstmann-Straussler-Scheinker Disease:Autopsy Study of a Familial Case
Ann Neurol 20:540-543, Vinters,H.V.,et al, 1986

Gerstmann-Straussler-Scheinker Disease with Coincidental Familial Onset
Ann Neurol 14:670-678, Hudson,A.J.,et al, 1983

Angular Gyrus Syndrome Simulating Alzheimer's Disease
Arch Neurol 39:616-620, Benson,D.F.,et al, 1982



Showing articles 0 to 22 of 22