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D E Bulman

Showing results (31-40 of 52) with videos related to

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American Journal of Human Genetics|May 1, 1992
Somatic reversion/suppression in Duchenne muscular dystrophy (DMD): evidence supporting a frame-restoring mechanism in rare dystrophin-positive fibersC J Klein, D D Coovert, D E Bulman, et al.
Neuromuscular Disorders : NMD|March 1, 1993
Sarcolemmal distribution of abnormal dystrophin in Xp21 carriersM Vainzof, L V Nicholson, D E Bulman, et al.
British Medical Bulletin|July 1, 1989
Myogenic regulation of dystrophin gene expressionH J Klamut, E E Zubrzycka-Gaarn, D E Bulman, et al.
Neurology|December 22, 1999
A novel sodium channel mutation in a family with hypokalemic periodic paralysisD E Bulman, K A Scoggan, M D van Oene, et al.
American Journal of Medical Genetics|April 1, 1991
Screening of male patients with autosomal recessive Duchenne dystrophy through dystrophin and DNA studiesM Vainzof, R C Pavanello, I Pavanello-Filho, et al.
Neurology|May 1, 1991
Dystrophin expression and somatic reversion in prednisone-treated and untreated Duchenne dystrophy. CIDD Study GroupK L Burrow, D D Coovert, C J Klein, et al.
Experimental Cell Research|January 1, 1991
Dystrophin is tightly associated with the sarcolemma of mammalian skeletal muscle fibersE E Zubrzycka-Gaarn, O F Hutter, G Karpati, et al.
Journal of Medical Genetics|October 1, 1996
X linked spondyloepiphyseal dysplasia: a clinical, radiological, and molecular study of a large kindredJ J MacKenzie, J Fitzpatrick, P Babyn, et al.
Human Molecular Genetics|June 1, 1993
Characterization of translational frame exception patients in Duchenne/Becker muscular dystrophyA V Winnard, C J Klein, D D Coovert, et al.
The New England Journal of Medicine|December 25, 1986
A population-based study of multiple sclerosis in twinsG C Ebers, D E Bulman, A D Sadovnick, et al.
Pageof 6

Showing results (31-40 of 52) with videos related to

Sort By:
Pageof 6
American Journal of Human Genetics|May 1, 1992
Somatic reversion/suppression in Duchenne muscular dystrophy (DMD): evidence supporting a frame-restoring mechanism in rare dystrophin-positive fibersC J Klein, D D Coovert, D E Bulman, et al.
Neuromuscular Disorders : NMD|March 1, 1993
Sarcolemmal distribution of abnormal dystrophin in Xp21 carriersM Vainzof, L V Nicholson, D E Bulman, et al.
British Medical Bulletin|July 1, 1989
Myogenic regulation of dystrophin gene expressionH J Klamut, E E Zubrzycka-Gaarn, D E Bulman, et al.
Neurology|December 22, 1999
A novel sodium channel mutation in a family with hypokalemic periodic paralysisD E Bulman, K A Scoggan, M D van Oene, et al.
American Journal of Medical Genetics|April 1, 1991
Screening of male patients with autosomal recessive Duchenne dystrophy through dystrophin and DNA studiesM Vainzof, R C Pavanello, I Pavanello-Filho, et al.
Neurology|May 1, 1991
Dystrophin expression and somatic reversion in prednisone-treated and untreated Duchenne dystrophy. CIDD Study GroupK L Burrow, D D Coovert, C J Klein, et al.
Experimental Cell Research|January 1, 1991
Dystrophin is tightly associated with the sarcolemma of mammalian skeletal muscle fibersE E Zubrzycka-Gaarn, O F Hutter, G Karpati, et al.
Journal of Medical Genetics|October 1, 1996
X linked spondyloepiphyseal dysplasia: a clinical, radiological, and molecular study of a large kindredJ J MacKenzie, J Fitzpatrick, P Babyn, et al.
Human Molecular Genetics|June 1, 1993
Characterization of translational frame exception patients in Duchenne/Becker muscular dystrophyA V Winnard, C J Klein, D D Coovert, et al.
The New England Journal of Medicine|December 25, 1986
A population-based study of multiple sclerosis in twinsG C Ebers, D E Bulman, A D Sadovnick, et al.
Pageof 6