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Differential
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akinetic mute
amyloid plaques
areflexia
ataxia
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ataxia, hereditary
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bovine spongiform encephalopathy
burning paresthesia
central nervous system, infection of
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cerebellar plaques, amyloid
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deep gray nuclei
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fatal familial insomnia
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genetic counselling
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genetic neurologic disorders
genetic testing
Gerstmann-Straussler-Scheinker disease
heralding manifestation
hyporeflexia
iatrogenic neurologic disorders
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, variant
kuru
molecular genetics
MRI
MRI, abnormal
MRI, diffusion weighted
neurofibrillary degeneration
neurologic disease, diagnoses of
neurologic signs
neuropathology
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Parkinsonism syndrome
polymerase chain reaction
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
single photon emission computed tomography
spongy degeneration of brain
tandem gait, ataxic
virus, slow
visual loss
weight loss
Western immunoblot test
Showing articles 0 to 22 of 22

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

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

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

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

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

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

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

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

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

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