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American Journal of Medical Genetics|October 1, 1992
Additional dystrophin fragment in Becker muscular dystrophy may result from proteolytic cleavage at deletion junctionsA H Beggs, E P Hoffman, L M KunkelClinical Chemistry|July 1, 1989
Molecular genetics of Duchenne and Becker muscular dystrophy: emphasis on improved diagnosisL M Kunkel, A H Beggs, E P HoffmanJournal of the Neurological Sciences|January 1, 1996
Recruitment of mast cells to muscle after mild damageJ R Gorospe, B K Nishikawa, E P HoffmanNeuromuscular Disorders : NMD|July 17, 1999
Prenatal diagnosis in a family affected with beta-sarcoglycan muscular dystrophyE Pegoraro, M Fanin, C Angelini, et al.Radiology|June 1, 1980
Computed tomography in acute pyelonephritis associated with diabetesE P Hoffman, R E Mindelzun, R U AndersonHuman Molecular Genetics|September 1, 1994
Pathophysiology of sodium channelopathies: correlation of normal/mutant mRNA ratios with clinical phenotype in dominantly inherited periodic paralysisJ Zhou, S J Spier, J Beech, et al.The Journal of Cell Biology|December 21, 2000
Expression profiling in the muscular dystrophies: identification of novel aspects of molecular pathophysiologyY W Chen, P Zhao, R Borup, et al.Neuromuscular Disorders : NMD|July 1, 1994
Dystrophin-deficient myofibers are vulnerable to mast cell granule-induced necrosisJ R Gorospe, M Tharp, T Demitsu, et al.American Journal of Medical Genetics|October 6, 1999
Unique PABP2 mutations in "Cajuns" suggest multiple founders of oculopharyngeal muscular dystrophy in populations with French ancestryP C Scacheri, C Garcia, R Hébert, et al.The American Journal of Physiology|January 14, 1999
Hyperkalemic periodic paralysis M1592V mutation modifies activation in human skeletal muscle Na+ channelC V Rojas, A Neely, G Velasco-Loyden, et al.Pageof 19