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Journal of Virology|November 1, 1996
The basal lamina is a physical barrier to herpes simplex virus-mediated gene delivery to mature muscle fibersJ Huard, W G Feero, S C Watkins, et al.
Obstetrics and Gynecology|December 1, 1994
Fetal muscle biopsy: collaborative experience with varied indicationsM I Evans, E P Hoffman, C Cadrin, et al.
Neurology|April 11, 2001
A new mutation in a family with cold-aggravated myotonia disrupts Na(+) channel inactivationF F Wu, M P Takahashi, E Pegoraro, et al.
Neurology|April 14, 2004
Large-scale disruption of microtubule pathways in morphologically normal human spastin muscleA Molon, S Di Giovanni, Y W Chen, et al.
Annals of Neurology|September 1, 1995
Primary adhalin deficiency as a cause of muscular dystrophy in patients with normal dystrophinA Ljunggren, D Duggan, E McNally, et al.
American Journal of Medical Genetics|January 30, 1995
Duchenne muscular dystrophy and myotonic dystrophy in the same patientA L Dubrovsky, A L Taratuto, G Sevlever, et al.
American Journal of Medical Genetics|June 28, 1996
Genetic counseling of isolated carriers of Duchenne muscular dystrophyE P Hoffman, E Pegoraro, P Scacheri, et al.
Annals of Neurology|November 1, 1990
Quadriceps myopathy: forme fruste of Becker muscular dystrophyN Sunohara, K Arahata, E P Hoffman, et al.
Neurology|March 24, 2004
Indian Agarwal megalencephalic leukodystrophy with cysts is caused by a common MLC1 mutationJ R Gorospe, B S Singhal, T Kainu, et al.
Human Molecular Genetics|May 20, 1999
Myotonic dystrophy: tissue-specific effect of somatic CTG expansions on allele-specific DMAHP/SIX5 expressionZ Korade-Mirnics, J Tarleton, S Servidei, et al.
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