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M Vainzof

Showing results (11-20 of 85) with videos related to

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Journal of the Neurological Sciences|July 1, 1995
Is dystrophin always altered in Becker muscular dystrophy patients?M Vainzof, M R Passos-Bueno, R C Pavanello, et al.
Neuromuscular Disorders : NMD|November 23, 2006
Mutation analysis in the FKRP gene provides an explanation for a rare cause of intrafamilial clinical variability in LGMD2IN M Vieira, D Schlesinger, F de Paula, et al.
Growth Regulation|March 1, 1991
Short stature in Duchenne muscular dystrophyD Rapaport, G M Colletto, M Vainzof, et al.
Journal of Medical Genetics|January 1, 1995
Myotonic dystrophy: genetic, clinical, and molecular analysis of patients from 41 Brazilian familiesM R Passos-Bueno, A Cerqueira, M Vainzof, et al.
Journal of Medical Genetics|July 1, 1992
A model to estimate the expression of the dystrophin gene in muscle from female Becker muscular dystrophy carriersM Vainzof, M R Passos-Bueno, R C Pavanello, et al.
American Journal of Medical Genetics|August 1, 1989
Nocturnal rhythm of growth hormone in Duchenne patients: effect of different doses of mazindol and/or cyproheptadineM Zatz, D Rapaport, R C Pavanello, et al.
Human Molecular Genetics|June 1, 1996
Linkage analysis in autosomal recessive limb-girdle muscular dystrophy (AR LGMD) maps a sixth form to 5q33-34 (LGMD2F) and indicates that there is at least one more subtype of AR LGMDM R Passos-Bueno, E S Moreira, M Vainzof, et al.
American Journal of Medical Genetics|June 15, 1991
Apparent association of mental retardation and specific patterns of deletions screened with probes cf56a and cf23a in Duchenne muscular dystrophyD Rapaport, M R Passos-Bueno, L Brandão, et al.
Genetic Testing|February 24, 2001
Does the A3333G mutation in the CACNL1A3 gene, detected in malignant hyperthermia, also occur in central core disease?M Vainzof, V P Muniz, A M Tsanaclis, et al.
Neurology|December 14, 2005
A family with McLeod syndrome and calpainopathy with clinically overlapping diseasesA Starling, D Schlesinger, F Kok, et al.
Pageof 9

Showing results (11-20 of 85) with videos related to

Sort By:
Pageof 9
Journal of the Neurological Sciences|July 1, 1995
Is dystrophin always altered in Becker muscular dystrophy patients?M Vainzof, M R Passos-Bueno, R C Pavanello, et al.
Neuromuscular Disorders : NMD|November 23, 2006
Mutation analysis in the FKRP gene provides an explanation for a rare cause of intrafamilial clinical variability in LGMD2IN M Vieira, D Schlesinger, F de Paula, et al.
Growth Regulation|March 1, 1991
Short stature in Duchenne muscular dystrophyD Rapaport, G M Colletto, M Vainzof, et al.
Journal of Medical Genetics|January 1, 1995
Myotonic dystrophy: genetic, clinical, and molecular analysis of patients from 41 Brazilian familiesM R Passos-Bueno, A Cerqueira, M Vainzof, et al.
Journal of Medical Genetics|July 1, 1992
A model to estimate the expression of the dystrophin gene in muscle from female Becker muscular dystrophy carriersM Vainzof, M R Passos-Bueno, R C Pavanello, et al.
American Journal of Medical Genetics|August 1, 1989
Nocturnal rhythm of growth hormone in Duchenne patients: effect of different doses of mazindol and/or cyproheptadineM Zatz, D Rapaport, R C Pavanello, et al.
Human Molecular Genetics|June 1, 1996
Linkage analysis in autosomal recessive limb-girdle muscular dystrophy (AR LGMD) maps a sixth form to 5q33-34 (LGMD2F) and indicates that there is at least one more subtype of AR LGMDM R Passos-Bueno, E S Moreira, M Vainzof, et al.
American Journal of Medical Genetics|June 15, 1991
Apparent association of mental retardation and specific patterns of deletions screened with probes cf56a and cf23a in Duchenne muscular dystrophyD Rapaport, M R Passos-Bueno, L Brandão, et al.
Genetic Testing|February 24, 2001
Does the A3333G mutation in the CACNL1A3 gene, detected in malignant hyperthermia, also occur in central core disease?M Vainzof, V P Muniz, A M Tsanaclis, et al.
Neurology|December 14, 2005
A family with McLeod syndrome and calpainopathy with clinically overlapping diseasesA Starling, D Schlesinger, F Kok, et al.
Pageof 9