The congenital muscular dystrophies in 2004: a century of exciting progress
- 1 October 2004
- journal article
- review article
- Published by Elsevier in Neuromuscular Disorders
- Vol. 14 (10) , 635-649
- https://doi.org/10.1016/j.nmd.2004.06.009
Abstract
No abstract availableKeywords
This publication has 95 references indexed in Scilit:
- Mutations of the Selenoprotein N Gene, Which Is Implicated in Rigid Spine Muscular Dystrophy, Cause the Classical Phenotype of Multiminicore Disease: Reassessing the Nosology of Early-Onset MyopathiesAmerican Journal of Human Genetics, 2002
- Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophyNature, 2002
- Post-translational disruption of dystroglycan–ligand interactions in congenital muscular dystrophiesNature, 2002
- Deficiency of α-Dystroglycan in Muscle–Eye–Brain DiseaseBiochemical and Biophysical Research Communications, 2002
- Congenital Muscular Dystrophy with Secondary Merosin Deficiency and Normal Brain MRI: A Novel Entity?Neuropediatrics, 2000
- Interaction of agrin with laminin requires a coiled-coil conformation of the agrin-binding site within the laminin gamma 1 chainThe EMBO Journal, 1999
- Laminin-2/Integrin Interactions Enhance Myelin Membrane Formation by OligodendrocytesMolecular and Cellular Neuroscience, 1999
- Changes of laminin β2 chain expression in congenital muscular dystrophyNeuromuscular Disorders, 1997
- 41st ENMC international workshop on congenital muscular dystrophy 8–10 March 1996, Naarden, The NetherlandsNeuromuscular Disorders, 1996
- Familial concordance of brain magnetic resonance imaging changes in congenital muscular dystrophyNeuromuscular Disorders, 1995