A case of progressive subcortical gliosis associated with deposition of abnormal prion protein (PrP)
Open Access
- 1 June 1995
- journal article
- Published by BMJ in Journal of Neurology, Neurosurgery & Psychiatry
- Vol. 58 (6), 759-760
- https://doi.org/10.1136/jnnp.58.6.759
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1Nature Genetics, 1994
- Absence of disease related prion protein in neurodegenerative disorders presenting with Parkinson's syndrome.Journal of Neurology, Neurosurgery & Psychiatry, 1994
- Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1Nature Genetics, 1993
- Dominantly inherited olivopontocerebellar atrophy from eastern CubaJournal of the Neurological Sciences, 1989
- A case of progressive subcortical gliosis presenting clinically as Steele-Richardson-Olszewski syndrome.Journal of Neurology, Neurosurgery & Psychiatry, 1988
- Low lumbar CSF levels of homovanillic acid and 5-hydroxyindoleacetic acid in multiple system atrophy with autonomic failure.Journal of Neurology, Neurosurgery & Psychiatry, 1988
- PROGRESSIVE SUBCORTICAL GLIOSIS, A RARE FORM OF PRESENILE DEMENTIABrain, 1967