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M Zatz

Showing results (201-210 of 252) with videos related to

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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.
Reproduction, Nutrition, Development|July 27, 1999
Melatonin synthesis pathway: circadian regulation of the genes encoding the key enzymes in the chicken pineal gland and retinaM Bernard, J Guerlotté, P Grève, et al.
Genetic Testing|May 4, 2000
Molecular analysis in Brazilian cystic fibrosis patients reveals five novel mutationsA L Bernardino, A Ferri, M R Passos-Bueno, et al.
American Journal of Medical Genetics|February 27, 1995
Why is the reproductive performance lower in Becker (BMD) as compared to limb girdle (LGMD) muscular dystrophy male patients?S Eggers, V Lauriano, M Melo, et al.
American Journal of Medical Genetics|July 24, 1998
Description of a new mutation and characterization of FGFR1, FGFR2, and FGFR3 mutations among Brazilian patients with syndromic craniosynostosesM R Passos-Bueno, A L Sertié, A Richieri-Costa, 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.
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.
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.
Revista Medica De Chile|October 29, 2000
[Post exercise myalgias as presentation form of dystrophinopathy]K Kleinsteuber, P Rocco, L Herrera, et al.
Pageof 26

Showing results (201-210 of 252) with videos related to

Sort By:
Pageof 26
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.
Reproduction, Nutrition, Development|July 27, 1999
Melatonin synthesis pathway: circadian regulation of the genes encoding the key enzymes in the chicken pineal gland and retinaM Bernard, J Guerlotté, P Grève, et al.
Genetic Testing|May 4, 2000
Molecular analysis in Brazilian cystic fibrosis patients reveals five novel mutationsA L Bernardino, A Ferri, M R Passos-Bueno, et al.
American Journal of Medical Genetics|February 27, 1995
Why is the reproductive performance lower in Becker (BMD) as compared to limb girdle (LGMD) muscular dystrophy male patients?S Eggers, V Lauriano, M Melo, et al.
American Journal of Medical Genetics|July 24, 1998
Description of a new mutation and characterization of FGFR1, FGFR2, and FGFR3 mutations among Brazilian patients with syndromic craniosynostosesM R Passos-Bueno, A L Sertié, A Richieri-Costa, 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.
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.
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.
Revista Medica De Chile|October 29, 2000
[Post exercise myalgias as presentation form of dystrophinopathy]K Kleinsteuber, P Rocco, L Herrera, et al.
Pageof 26