Fukuyama congenital muscular dystrophy: Cortical dysplasia of the cerebrum in a 20 week fetus
- 1 September 1996
- journal article
- Published by Wiley in Neuropathology
- Vol. 16 (3) , 184-189
- https://doi.org/10.1111/j.1440-1789.1996.tb00180.x
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Are breaches in the glia limitans the primary cause of the micropolygyria in Fukuyama-type congenital muscular dystrophy (FCMD)? - Pathological study of the cerebral cortex of an FCDM fetusActa Neuropathologica, 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
- Gross and Microscopic Development of the Central Nervous SystemPublished by Springer Nature ,1989
- 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