Merosin-deficient congenital muscular dystrophy associated with abnormal cerebral cortical gyration: an autopsy study
- 1 March 1999
- journal article
- case report
- Published by Elsevier in Neuromuscular Disorders
- Vol. 9 (2) , 86-94
- https://doi.org/10.1016/s0960-8966(98)00112-6
Abstract
No abstract availableKeywords
This publication has 25 references indexed in Scilit:
- Presence of Laminin α5 Chain and Lack of Laminin α1 Chain during Human Muscle Development and in Muscular DystrophiesJournal of Biological Chemistry, 1997
- Expression of Laminin Chains in Skin in Merosin-Deficient Congenital Muscular DystrophyNeuropediatrics, 1997
- Magnetic resonance imaging in classification of congenital muscular dystrophies with brain abnormalitiesAnnals of Neurology, 1997
- Intracellular detection of laminin α2 chain in skin by electron microscopy immunocytochemistry: Comparison between normal and laminin α2 chain deficient subjectsNeuromuscular Disorders, 1997
- Peripheral nerve involvement in merosin-deficient congenital muscular dystrophy and dy mouseNeuromuscular Disorders, 1997
- Pial-glial barrier abnormalities in fetuses with Fukuyama congenital muscular dystrophyBrain & Development, 1997
- Sequential study of central and peripheral nervous system involvement in an infant with merosin-deficient congenital muscular dystrophyNeuromuscular Disorders, 1996
- Fukuyama congenital muscular dystrophy: Cortical dysplasia of the cerebrum in a 20 week fetusNeuropathology, 1996
- Merosin-negative congenital muscular dystrophy, occipital epilepsy with periodic spasms and focal cortical dysplasia. Report of three Italian cases in two familiesBrain & Development, 1996
- Somatosensory and Visual Evoked Potentials in Congenital Muscular Dystrophy: Correlation with MRI Changes and Muscle Merosin StatusNeuropediatrics, 1995