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M Vainzof

Showing results (51-60 of 85) with videos related to

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Neuromuscular Disorders : NMD|March 1, 1993
Sarcolemmal distribution of abnormal dystrophin in Xp21 carriersM Vainzof, L V Nicholson, D E Bulman, et al.
Journal of the Neurological Sciences|April 1, 1991
Serum creatine-kinase (CK) and pyruvate-kinase (PK) activities in Duchenne (DMD) as compared with Becker (BMD) muscular dystrophyM Zatz, D Rapaport, M Vainzof, et al.
American Journal of Medical Genetics|December 18, 1998
Absence of correlation between skewed X inactivation in blood and serum creatine-kinase levels in Duchenne/Becker female carriersD R Sumita, M Vainzof, S Campiotto, et al.
American Journal of Human Genetics|January 1, 1995
High proportion of new mutations and possible anticipation in Brazilian facioscapulohumeral muscular dystrophy familiesM Zatz, S K Marie, M R Passos-Bueno, et al.
Neuromuscular Disorders : NMD|January 1, 1991
Dystrophin immunofluorescence pattern in manifesting and asymptomatic carriers of Duchenne's and Becker muscular dystrophies of different agesM Vainzof, R C Pavanello, I Pavanello, et al.
Journal of the Neurological Sciences|April 1, 1991
Exclusion of the gene responsible for facioscapulohumeral muscular dystrophy (FSH) at 6q23-q27M R Passos-Bueno, B Byth, D Love, et al.
Neuromuscular Disorders : NMD|July 23, 2014
Milder course in Duchenne patients with nonsense mutations and no muscle dystrophinM Zatz, R C M Pavanello, M Lazar, et al.
Neuropediatrics|August 1, 1997
Deficiency of alpha-actinin-3 (ACTN3) occurs in different forms of muscular dystrophyM Vainzof, C S Costa, S K Marie, et al.
Anaesthesia Reports|July 10, 2025
Association between joint dislocation and malignant hyperthermiaA O Gomes, P V Andrade, J M Santos, 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.
Pageof 9

Showing results (51-60 of 85) with videos related to

Sort By:
Pageof 9
Neuromuscular Disorders : NMD|March 1, 1993
Sarcolemmal distribution of abnormal dystrophin in Xp21 carriersM Vainzof, L V Nicholson, D E Bulman, et al.
Journal of the Neurological Sciences|April 1, 1991
Serum creatine-kinase (CK) and pyruvate-kinase (PK) activities in Duchenne (DMD) as compared with Becker (BMD) muscular dystrophyM Zatz, D Rapaport, M Vainzof, et al.
American Journal of Medical Genetics|December 18, 1998
Absence of correlation between skewed X inactivation in blood and serum creatine-kinase levels in Duchenne/Becker female carriersD R Sumita, M Vainzof, S Campiotto, et al.
American Journal of Human Genetics|January 1, 1995
High proportion of new mutations and possible anticipation in Brazilian facioscapulohumeral muscular dystrophy familiesM Zatz, S K Marie, M R Passos-Bueno, et al.
Neuromuscular Disorders : NMD|January 1, 1991
Dystrophin immunofluorescence pattern in manifesting and asymptomatic carriers of Duchenne's and Becker muscular dystrophies of different agesM Vainzof, R C Pavanello, I Pavanello, et al.
Journal of the Neurological Sciences|April 1, 1991
Exclusion of the gene responsible for facioscapulohumeral muscular dystrophy (FSH) at 6q23-q27M R Passos-Bueno, B Byth, D Love, et al.
Neuromuscular Disorders : NMD|July 23, 2014
Milder course in Duchenne patients with nonsense mutations and no muscle dystrophinM Zatz, R C M Pavanello, M Lazar, et al.
Neuropediatrics|August 1, 1997
Deficiency of alpha-actinin-3 (ACTN3) occurs in different forms of muscular dystrophyM Vainzof, C S Costa, S K Marie, et al.
Anaesthesia Reports|July 10, 2025
Association between joint dislocation and malignant hyperthermiaA O Gomes, P V Andrade, J M Santos, 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.
Pageof 9