Electroretinogram in Duchenne/Becker Muscular Dystrophy
- 1 April 1998
- journal article
- research article
- Published by Elsevier in Pediatric Neurology
- Vol. 18 (4) , 315-320
- https://doi.org/10.1016/s0887-8994(97)00208-7
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- Duchenne muscular dystrophy: negative electroretinograms and normal dark adaptation. Reappraisal of assignment of X linked incomplete congenital stationary night blindness.Journal of Medical Genetics, 1995
- Correlation between electroretinogram findings and molecular analysis in the Duchenne muscular dystrophy phenotype.British Journal of Ophthalmology, 1994
- Retinal signal transmission in Duchenne muscular dystrophy: evidence for dysfunction in the photoreceptor/depolarizing bipolar cell pathway.Journal of Clinical Investigation, 1994
- Characterization of the Ocular Phenotype of Duchenne and Becker Muscular DystrophyOphthalmology, 1994
- Dystrophin expression in the human retina is required for normal function as defined by electroretinographyNature Genetics, 1993
- The structural and functional diversity of dystrophinNature Genetics, 1993
- The Electroretinogram in Infants and Young ChildrenJournal Of Clinical Neurophysiology, 1992
- Dystrophin: Localization and presumed functionMuscle & Nerve, 1991
- Detection of 98% of DMD/BMD gene deletions by polymerase chain reactionHuman Genetics, 1990
- Standard for Clinical ElectroretinographyArchives of Ophthalmology (1950), 1989