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S K Marie

Showing results (21-30 of 45) with videos related to

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Journal of the Neurological Sciences|May 1, 1994
Assessment of the 50-kDa dystrophin-associated glycoprotein in Brazilian patients with severe childhood autosomal recessive muscular dystrophyM Zatz, K Matsumura, M Vainzof, et al.
American Journal of Medical Genetics|May 8, 2000
Brazilian family with pure autosomal dominant spastic paraplegia maps to 8q: analysis of muscle beta 1 syntrophinP Rocco, M Vainzof, S C Froehner, et al.
Neuropediatrics|December 1, 1995
Deficiency of merosin (laminin M or alpha 2) in congenital muscular dystrophy associated with cerebral white matter alterationsM Vainzof, S K Marie, U C Reed, et al.
Annals of the New York Academy of Sciences|September 18, 2009
Anti-C1q antibodies in juvenile-onset systemic lupus erythematosusA A Jesus, C A Silva, M Carneiro-Sampaio, et al.
Arquivos De Neuro-Psiquiatria|March 1, 1995
Autosomal recessive nondystrophic myotonia. Report of a case with unusual clinical courseU C Reed, S K Marie, M W Brotto, 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.
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.
The Journal of Pathology|May 1, 2001
Histopathological findings in skeletal muscle used in human dynamic cardiomyoplastyP S Gutierrez, W O Pires, S K Marie, 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.
Pageof 5

Showing results (21-30 of 45) with videos related to

Sort By:
Pageof 5
Journal of the Neurological Sciences|May 1, 1994
Assessment of the 50-kDa dystrophin-associated glycoprotein in Brazilian patients with severe childhood autosomal recessive muscular dystrophyM Zatz, K Matsumura, M Vainzof, et al.
American Journal of Medical Genetics|May 8, 2000
Brazilian family with pure autosomal dominant spastic paraplegia maps to 8q: analysis of muscle beta 1 syntrophinP Rocco, M Vainzof, S C Froehner, et al.
Neuropediatrics|December 1, 1995
Deficiency of merosin (laminin M or alpha 2) in congenital muscular dystrophy associated with cerebral white matter alterationsM Vainzof, S K Marie, U C Reed, et al.
Annals of the New York Academy of Sciences|September 18, 2009
Anti-C1q antibodies in juvenile-onset systemic lupus erythematosusA A Jesus, C A Silva, M Carneiro-Sampaio, et al.
Arquivos De Neuro-Psiquiatria|March 1, 1995
Autosomal recessive nondystrophic myotonia. Report of a case with unusual clinical courseU C Reed, S K Marie, M W Brotto, 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.
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.
The Journal of Pathology|May 1, 2001
Histopathological findings in skeletal muscle used in human dynamic cardiomyoplastyP S Gutierrez, W O Pires, S K Marie, 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.
Pageof 5