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Muscle & Nerve|June 8, 2000
Partial alpha-sarcoglycan deficiency with retention of the dystrophin-glycoprotein complex in a LGMD2D familyM Vainzof, E S Moreira, M Canovas, 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.
Stem Cell Reviews and Reports|September 8, 2010
Human multipotent mesenchymal stromal cells from distinct sources show different in vivo potential to differentiate into muscle cells when injected in dystrophic miceN M Vieira, E Zucconi, C R Bueno, et al.
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.
Journal of Medical Genetics|February 1, 1993
Cosegregation of schizophrenia with Becker muscular dystrophy: susceptibility locus for schizophrenia at Xp21 or an effect of the dystrophin gene in the brain?M Zatz, H Vallada, M S Melo, 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.
Journal of the Neurological Sciences|February 1, 1991
Immunofluorescence dystrophin study in Duchenne dystrophy through the concomitant use of two antibodies directed against the carboxy-terminal and the amino-terminal region of the proteinM Vainzof, E E Zubrzycka-Gaarn, D Rapaport, 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.
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 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.
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