Mary S. Carvalho

Pompe disease in a Brazilian series: clinical and molecular analyses with identification of nine new mutations

Sueli Mieko Oba‐Shinjo, Roseli da Silva, Fernanda Gonçalves de Andrade et al. · Journal of Neurology · 2009 · 60 citations

Life Sciences, Genetics, Molecular Genetics +12

Nebulin expression in patients with nemaline myopathy

Juliana Gurgel‐Giannetti, Umbertina C. Reed, Marie‐Louise Bang et al. · Neuromuscular Disorders · 2001 · 45 citations

Medicine, Neurology, Pathology +7

Merosin-deficient congenital muscular dystrophy (CMD): a study of 25 Brazilian patients using MRI

Cláudia da Costa Leite, Leandro Tavares Lucato, Maria da Graça Morais Martin et al. · Pediatric Radiology · 2005 · 44 citations

Medicine, Anatomy, Radiology +11

Comparison of motor strength and function in patients with Duchenne muscular dystrophy with or without steroid therapy

Samara Lamounier Santana Parreira, Maria Bernadete Dutra de Resende, Edmar Zanoteli et al. · Arquivos de Neuro-Psiquiatria · 2010 · 33 citations · Full text

Medicine, Neurology, Motor Development +16

Merosin-positive congenital muscular dystrophy in two siblings with cataract and slight mental retardation

Umbertina Conti Reed, Ana Maria Crous Tsanaclis, Mariz Vainzof et al. · Brain and Development · 1999 · 29 citations

Medicine, Genetics, Pediatrics +8