Glial cytoplasmic inclusions in the CNS of patients with multiple system atrophy (striatonigral degeneration, olivopontocerebellar atrophy and Shy-Drager syndrome)

MI Papp, JE Kahn, PL Lantos - Journal of the neurological sciences, 1989 - Elsevier
Glial cytoplasmic inclusions (GCIs) were demonstrated by silver staining,
immunocytochemistry and by electron microscopy in the central nervous system (CNS) of 11 …

Preliminary NINDS neuropathologic criteria for Steele‐Richardson‐Olszewski syndrome (progressive supranuclear palsy)

JJ Hauw, SE Daniel, D Dickson, DS Horoupian… - Neurology, 1994 - AAN Enterprises
We present the preliminary neuropathologic criteria for progressive supranuclear palsy
(PSP) as proposed at a workshop held at the National Institutes of Health, Bethesda, MD …

HIV-associated disease of the nervous system: review of nomenclature and proposal for neuropathology-based terminology

H Budka, CA Wiley, P Kleihues, J Artigas… - Brain …, 1991 - mayoclinic.elsevierpure.com
HIV-associated disease of the nervous system: Review of nomenclature and proposal for
neuropathology-based terminology — Mayo Clinic Skip to main navigation Skip to search Skip …

Filamentous α-synuclein inclusions link multiple system atrophy with Parkinson's disease and dementia with Lewy bodies

MG Spillantini, RA Crowther, R Jakes, NJ Cairns… - Neuroscience …, 1998 - Elsevier
α-Synuclein forms the major component of Lewy bodies and Lewy neurites, the defining
neuropathological characteristics of Parkinson's disease and dementia with Lewy bodies …

Neuropathological diagnostic criteria for Creutzfeldt‐Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases)

H Budka, A Aguzzi, P Brown, JM Brucher… - Brain …, 1995 - Wiley Online Library
Neuropathological diagnostic criteria for Creutzfeldt‐Jakob disease (CJD) and other human
transmissible spongiform encephalopathies (prion diseases) are proposed for the following …

Investigation of variant Creutzfeldt-Jakob disease and other human prion diseases with tonsil biopsy samples

AF Hill, RJ Butterworth, S Joiner, G Jackson… - The Lancet, 1999 - thelancet.com
Background Prion diseases are associated with the accumulation of an abnormal isoformof
cellular prion protein (PrP Sc), which is the principal constituent of prions. Prions replicate in …

Office of Rare Diseases neuropathologic criteria for corticobasal degeneration

DW Dickson, C Bergeron, SS Chin… - … of Neuropathology & …, 2002 - academic.oup.com
A working group supported by the Office of Rare Diseases of the National Institutes of Health
formulated neuropathologic criteria for corticobasal degeneration (CBD) that were …

Validity of current clinical criteria for Alzheimer's disease, vascular dementia and dementia with Lewy bodies

C Holmes, N Cairns, PL Lantos… - The British Journal of …, 1999 - cambridge.org
BackgroundFollowing the success of the NINCDS–ADRDA criteria for Alzheimer's disease,
groups interested in vascular dementia and dementia with Lewy bodies have now adopted …

Species-barrier-independent prion replication in apparently resistant species

AF Hill, S Joiner, J Linehan… - Proceedings of the …, 2000 - National Acad Sciences
Transmission of prions between mammalian species is thought to be limited by a “species
barrier,” which depends on differences in the primary structure of prion proteins in the …

Validity and reliability of the preliminary NINDS neuropathologic criteria for progressive supranuclear palsy and related disorders

I Litvan, JJ Hauw, JJ Bartko, PL Lantos… - … of Neuropathology & …, 1996 - academic.oup.com
We investigated the validity and reliability of diagnoses made by eight neuropathologists
who used the preliminary NINDS neuropathologic diagnostic criteria for progressive …