rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
2
|
pubmed:dateCreated |
1997-7-17
|
pubmed:abstractText |
Orthochromatic leukodystrophy with pigmented glia and scavenger cells is a rare leukodystrophy of unknown etiology. This report describes a 42-year-old man with a history of depression, dementia and parkinsonism having the pathological features of orthochromatic leukodystrophy with pigmented glia.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
May
|
pubmed:issn |
0317-1671
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:volume |
24
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
146-50
|
pubmed:dateRevised |
2004-11-17
|
pubmed:meshHeading |
pubmed-meshheading:9164693-Adult,
pubmed-meshheading:9164693-Brain,
pubmed-meshheading:9164693-Brain Diseases,
pubmed-meshheading:9164693-Fatal Outcome,
pubmed-meshheading:9164693-Glial Fibrillary Acidic Protein,
pubmed-meshheading:9164693-Humans,
pubmed-meshheading:9164693-Kidney,
pubmed-meshheading:9164693-Liver,
pubmed-meshheading:9164693-Male,
pubmed-meshheading:9164693-Microscopy, Electron,
pubmed-meshheading:9164693-Neuroglia,
pubmed-meshheading:9164693-Pigmentation,
pubmed-meshheading:9164693-Spleen
|
pubmed:year |
1997
|
pubmed:articleTitle |
A rare form of adult onset leukodystrophy: orthochromatic leukodystrophy with pigmented glia.
|
pubmed:affiliation |
Department of Pathology, University of Toronto, Ontario, Canada.
|
pubmed:publicationType |
Journal Article,
Case Reports
|