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M Vainzof

Showing results (61-70 of 85) with videos related to

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Nature Genetics|October 1, 1996
Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan geneV Nigro, E de Sá Moreira, G Piluso, et al.
Neuromuscular Disorders : NMD|January 1, 1992
A deletion including the brain promoter of the Duchenne muscular dystrophy gene is not associated with mental retardationD Rapaport, M R Passos-Bueno, R I Takata, et al.
Revista Medica De Chile|October 29, 2000
[Post exercise myalgias as presentation form of dystrophinopathy]K Kleinsteuber, P Rocco, L Herrera, et al.
Brain & Development|July 7, 1999
Merosin-positive congenital muscular dystrophy in two siblings with cataract and slight mental retardationU C Reed, A M Tsanaclis, M Vainzof, et al.
Genomics|May 1, 1995
Confirmation of the 2p locus for the mild autosomal recessive limb-girdle muscular dystrophy gene (LGMD2B) in three families allows refinement of the candidate regionM R Passos-Bueno, R Bashir, E S Moreira, et al.
Journal of Medical Genetics|May 1, 1993
Evidence of genetic heterogeneity in the autosomal recessive adult forms of limb-girdle muscular dystrophy following linkage analysis with 15q probes in Brazilian familiesM R Passos-Bueno, I Richard, M Vainzof, et al.
Human Molecular Genetics|November 1, 1993
Genetic heterogeneity for Duchenne-like muscular dystrophy (DLMD) based on linkage and 50 DAG analysisM R Passos-Bueno, J R Oliveira, E Bakker, et al.
Biochemical and Biophysical Research Communications|July 11, 2001
Characterization of human skeletal muscle Ankrd2A Pallavicini, S Kojić, C Bean, et al.
Human Molecular Genetics|July 1, 1995
A common missense mutation in the adhalin gene in three unrelated Brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophyM R Bueno, E S Moreira, M Vainzof, et al.
Journal of the Neurological Sciences|March 10, 1997
Absence of calpain 3 in a form of limb-girdle muscular dystrophy (LGMD2A)M J Spencer, J G Tidball, L V Anderson, et al.
Pageof 9

Showing results (61-70 of 85) with videos related to

Sort By:
Pageof 9
Nature Genetics|October 1, 1996
Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan geneV Nigro, E de Sá Moreira, G Piluso, et al.
Neuromuscular Disorders : NMD|January 1, 1992
A deletion including the brain promoter of the Duchenne muscular dystrophy gene is not associated with mental retardationD Rapaport, M R Passos-Bueno, R I Takata, et al.
Revista Medica De Chile|October 29, 2000
[Post exercise myalgias as presentation form of dystrophinopathy]K Kleinsteuber, P Rocco, L Herrera, et al.
Brain & Development|July 7, 1999
Merosin-positive congenital muscular dystrophy in two siblings with cataract and slight mental retardationU C Reed, A M Tsanaclis, M Vainzof, et al.
Genomics|May 1, 1995
Confirmation of the 2p locus for the mild autosomal recessive limb-girdle muscular dystrophy gene (LGMD2B) in three families allows refinement of the candidate regionM R Passos-Bueno, R Bashir, E S Moreira, et al.
Journal of Medical Genetics|May 1, 1993
Evidence of genetic heterogeneity in the autosomal recessive adult forms of limb-girdle muscular dystrophy following linkage analysis with 15q probes in Brazilian familiesM R Passos-Bueno, I Richard, M Vainzof, et al.
Human Molecular Genetics|November 1, 1993
Genetic heterogeneity for Duchenne-like muscular dystrophy (DLMD) based on linkage and 50 DAG analysisM R Passos-Bueno, J R Oliveira, E Bakker, et al.
Biochemical and Biophysical Research Communications|July 11, 2001
Characterization of human skeletal muscle Ankrd2A Pallavicini, S Kojić, C Bean, et al.
Human Molecular Genetics|July 1, 1995
A common missense mutation in the adhalin gene in three unrelated Brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophyM R Bueno, E S Moreira, M Vainzof, et al.
Journal of the Neurological Sciences|March 10, 1997
Absence of calpain 3 in a form of limb-girdle muscular dystrophy (LGMD2A)M J Spencer, J G Tidball, L V Anderson, et al.
Pageof 9