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  • Agnes Lumi Nishimura, Miguel Mitne-Neto, +9 authors Mayana Zatz
  • Medicine, Biology
  • American journal of human genetics
  • 2004 (First Publication: 1 November 2004)
  • Motor neuron diseases (MNDs) are a group of neurodegenerative disorders with involvement of upper and/or lower motor neurons, such as amyotrophic lateral sclerosis (ALS), spinal muscular atrophyContinue Reading
  • Natássia M. Vieira, Vanessa Brandalise, Eder Zucconi, Mariane Secco, Bryan E. Strauss, Mayana Zatz
  • Medicine, Biology
  • Cell transplantation
  • 2010 (First Publication: 1 March 2010)
  • Adipose tissue may represent a potential source of adult stem cells for tissue engineering applications in veterinary medicine. It can be obtained in large quantities, under local anesthesia, andContinue Reading
  • Eloisa de Sá Moreira, Tim Wiltshire, +8 authors Dieter E. Jenne
  • Biology, Medicine
  • Nature Genetics
  • 2000 (First Publication: 1 February 2000)
  • Autosomal recessive limb-girdle muscular dystrophies (AR LGMDs) are a genetically heterogeneous group of disorders that affect mainly the proximal musculature. There are eight genetically distinctContinue Reading
  • Rumaisa Bashir, Steven Loyal Britton, +15 authors Kate Bushby
  • Biology, Medicine
  • Nature Genetics
  • 1998 (First Publication: 1 September 1998)
  • The limb-girdle muscular dystrophies are a genetically heterogeneous group of inherited progressive muscle disorders that affect mainly the proximal musculature, with evidence for at least threeContinue Reading
  • Agnes Lumi Nishimura, Miguel Mitne-Neto, Helga C. A. Silva, João Ricardo Mendes Oliveira, Mariz Vainzof, Mayana Zatz
  • Biology, Medicine
  • Journal of Medical Genetics
  • 2004 (First Publication: 1 April 2004)
  • Motor neurone disease includes a heterogeneous group of disorders with motor neurone involvement, such as amyotrophic lateral sclerosis, progressive muscular atrophy, progressive bulbar palsy, andContinue Reading
  • Andrea L Sertié, V Sossi, Anamaria A. Camargo, Mayana Zatz, Christina Brahe, Maria Rita Santos Passos-Bueno
  • Biology, Medicine
  • Human molecular genetics
  • 2000 (First Publication: 12 August 2000)
  • Knobloch syndrome (KS) is an autosomal recessive disorder defined by the occurrence of high myopia, vitreoretinal degeneration with retinal detachment, macular abnormalities and occipitalContinue Reading