Pial-glial barrier abnormalities in fetuses with Fukuyama congenital muscular dystrophy
- 1 January 1997
- journal article
- case report
- Published by Elsevier in Brain & Development
- Vol. 19 (1) , 35-42
- https://doi.org/10.1016/s0387-7604(96)00056-3
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- Fukuyama congenital muscular dystrophy: Cortical dysplasia of the cerebrum in a 20 week fetusNeuropathology, 1996
- Dystrophin–glycoprotein complex: Its role in the molecular pathogenesis of muscular dystrophiesMuscle & Nerve, 1994
- Fukuyama Type Congenital Progressive Muscular Dystrophy (FCMD) – Special Comment on the Relationship Between the Case Reported by Nakayama et a1 and FCMD –Neuropathology, 1993
- Localization of a gene for Fukuyama type congenital muscular dystrophy to chromosome 9q31–33Nature Genetics, 1993
- Abnormal localization of laminin subunits in muscular dystrophiesJournal of the Neurological Sciences, 1993
- Destruction of meningeal cells over the newborn hamster cerebellum with 6-hydroxydopamine prevents foliation and lamination in the rostral cerebellumNeuroscience, 1986
- Meningeal cells are involved in foliation, lamination, and neurogenesis of the cerebellum: Evidence from 6-hydroxydopamine-induced destruction of meningeal cellsDevelopmental Biology, 1985
- Congenital progressive muscular dystrophy of the fukuyama type — clinical, genetic and pathological considerations —Brain & Development, 1981
- Congenital Muscular Dystrophy as a Disease of the Central Nervous SystemArchives of Neurology, 1976
- Neuronal migration, with special reference to developing human brain: a reviewBrain Research, 1973