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Neurology|October 1, 1996
Myotonia and the muscle chloride channel: dominant mutations show variable penetrance and founder effectP P Koty, E Pegoraro, G Hobson, et al.Gene Therapy|July 1, 1997
Selection and use of ligands for receptor-mediated gene delivery to myogenic cellsW G Feero, S Li, J D Rosenblatt, et al.Proceedings of the National Academy of Sciences of the United States of America|September 1, 1989
Dystrophin diagnosis: comparison of dystrophin abnormalities by immunofluorescence and immunoblot analysesK Arahata, E P Hoffman, L M Kunkel, et al.American Journal of Obstetrics and Gynecology|September 11, 1991
In utero fetal muscle biopsy for the diagnosis of Duchenne muscular dystrophyM I Evans, A Greb, L M Kunkel, et al.The Journal of Gene Medicine|March 30, 2000
Herpes simplex virus vector-mediated dystrophin gene transfer and expression in MDX mouse skeletal muscleG R Akkaraju, J Huard, E P Hoffman, et al.American Journal of Human Genetics|July 1, 1991
Exploring the molecular basis for variability among patients with Becker muscular dystrophy: dystrophin gene and protein studiesA H Beggs, E P Hoffman, J R Snyder, et al.Neuromuscular Disorders : NMD|March 27, 1999
Cardiac transplantation in a Duchenne muscular dystrophy carrierP Melacini, M Fanin, A Angelini, et al.Annals of Neurology|June 21, 2001
Gentamicin treatment of Duchenne and Becker muscular dystrophy due to nonsense mutationsK R Wagner, S Hamed, D W Hadley, et al.Journal of Medical Genetics|January 16, 1998
Genetic epidemiology of muscular dystrophies resulting from sarcoglycan gene mutationsM Fanin, D J Duggan, M L Mostacciuolo, et al.American Journal of Obstetrics and Gynecology|September 25, 2001
A novel X chromosome-linked genetic cause of recurrent spontaneous abortionM C Lanasa, W A Hogge, C J Kubik, et al.Pageof 19