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Human Gene Therapy|July 31, 1999
Polylysine modification of adenoviral fiber protein enhances muscle cell transductionK Bouri, W G Feero, M M Myerburg, et al.Fetal Diagnosis and Therapy|March 1, 1995
In utero fetal muscle biopsy alters diagnosis and carrier risks in Duchenne and Becker muscular dystrophyM I Evans, E L Krivchenia, M P Johnson, et al.Annals of Neurology|March 1, 1994
Elevated basic fibroblast growth factor in the serum of patients with Duchenne muscular dystrophyP A D'Amore, R H Brown, P T Ku, et al.Genomics|May 18, 1999
Human bHLH transcription factor gene myogenin (MYOG): genomic sequence and negative mutation analysis in patients with severe congenital myopathiesB S Tseng, S T Cavin, E P Hoffman, et al.Pediatric Research|May 1, 1995
Medium chain acyl-CoA dehydrogenase deficiency in Pennsylvania: neonatal screening shows high incidence and unexpected mutation frequenciesR Ziadeh, E P Hoffman, D N Finegold, et al.American Journal of Medical Genetics|March 31, 1997
Asymptomatic dystrophinopathyA Morrone, E Zammarchi, P C Scacheri, et al.Annals of Neurology|March 1, 1995
Hyperkalemic periodic paralysis with cardiac dysrhythmia: a novel sodium channel mutation?J L Baquero, R A Ayala, J Wang, et al.Journal of the Neurological Sciences|July 1, 1992
Dystrophin deficiency causes lethal muscle hypertrophy in catsF P Gaschen, E P Hoffman, J R Gorospe, et al.Neurology|February 28, 2002
Novel mutations in collagen VI genes: expansion of the Bethlem myopathy phenotypeP C Scacheri, E M Gillanders, S H Subramony, et al.Neurology|April 2, 1999
Calpain III mutation analysis of a heterogeneous limb-girdle muscular dystrophy populationF L Chou, C Angelini, D Daentl, et al.Pageof 19