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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.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.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.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.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.Journal of Neurochemistry|July 1, 1985
Denervation supersensitivity of the rat pineal to norepinephrine-stimulated [3H]inositide turnover revealed by lithium and a convenient procedureM ZatzPageof 26