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Neurology|November 9, 2000
A novel laminin alpha2 isoform in severe laminin alpha2 deficient congenital muscular dystrophyE Pegoraro, M Fanin, C P Trevisan, et al.Journal of the American Veterinary Medical Association|August 15, 1996
Laryngeal and pharyngeal dysfunction in horses homozygous for hyperkalemic periodic paralysisE A Carr, S J Spier, G D Kortz, et al.Journal of the Neurological Sciences|September 1, 1996
alpha-Sarcoglycan (adhalin) deficiency: complete deficiency patients are 5% of childhood-onset dystrophin-normal muscular dystrophy and most partial deficiency patients do not have gene mutationsD J Duggan, M Fanin, E Pegoraro, et al.Nature|June 30, 1988
Immunoelectron microscopic localization of dystrophin in myofibresS C Watkins, E P Hoffman, H S Slayter, et al.The New England Journal of Medicine|February 27, 1997
Mutations in the sarcoglycan genes in patients with myopathyD J Duggan, J R Gorospe, M Fanin, et al.Neurology|May 1, 1990
Enormous dystrophin in a patient with Becker muscular dystrophyC Angelini, A H Beggs, E P Hoffman, et al.The Journal of Clinical Investigation|April 1, 1997
RNA metabolism in myotonic dystrophy: patient muscle shows decreased insulin receptor RNA and protein consistent with abnormal insulin resistanceA Morrone, E Pegoraro, C Angelini, et al.Neurology|September 1, 1991
The frequency of patients with dystrophin abnormalities in a limb-girdle patient populationE Arikawa, E P Hoffman, M Kaido, et al.American Journal of Human Genetics|October 1, 1992
Fluorescent multiplex linkage analysis and carrier detection for Duchenne/Becker muscular dystrophyL S Schwartz, J Tarleton, B Popovich, et al.American Journal of Human Genetics|June 1, 1989
Dystrophin analysis in clonal myoblasts derived from a Duchenne muscular dystrophy carrierO Hurko, E P Hoffman, L McKee, et al.Pageof 19