The Molecular Pathogenesis of Pelizaeus-Merzbacher Disease
- 1 October 1999
- journal article
- review article
- Published by American Medical Association (AMA) in Archives of Neurology
- Vol. 56 (10) , 1210-1214
- https://doi.org/10.1001/archneur.56.10.1210
Abstract
Review from JAMA Neurology — The Molecular Pathogenesis of Pelizaeus-Merzbacher DiseaseKeywords
This publication has 21 references indexed in Scilit:
- Axonal Swellings and Degeneration in Mice Lacking the Major Proteolipid of MyelinScience, 1998
- Duplication of the proteolipid protein gene is the major cause of Pelizaeus‐Merzbacher diseaseNeurology, 1998
- Disrupted Proteolipid Protein Trafficking Results in Oligodendrocyte Apoptosis in an Animal Model of Pelizaeus-Merzbacher DiseaseThe Journal of cell biology, 1998
- Proteolipid Protein Is Necessary in Peripheral as Well as Central MyelinNeuron, 1997
- Assembly of CNS Myelin in the Absence of Proteolipid ProteinNeuron, 1997
- A cellular mechanism governing the severity of Pelizaeus–Merzbacher diseaseNature Genetics, 1996
- X-Linked Developmental Defects of Myelination: From Mouse Mutants to Human Genetic DiseasesThe Neuroscientist, 1996
- Many naturally occurring mutations of myelin proteolipid protein impair its intracellular transportJournal of Neuroscience Research, 1994
- Genetics of Pelizaeus-Merzbacher DiseaseDevelopmental Neuroscience, 1993
- Pelizaeus-Merzbacher Disease: Clinical and Nosological StudyJournal of Child Neurology, 1986