Lydia U. Yamamoto

Asymptomatic carriers for homozygous novel mutations in the FKRP gene: the other end of the spectrum

Flavia Paula, Natássia M. Vieira, Alessandra Starling et al. · European Journal of Human Genetics · 2003 · 78 citations · Full text

Life Sciences, Genetics, Molecular Genetics +4

Prenatal diagnosis in laminin α2 chain (merosin)-deficient congenital muscular dystrophy: A collective experience of five international centers

Mariz Vainzof, Pascale Richard, Ralf Herrmann et al. · Neuromuscular Disorders · 2005 · 41 citations · Full text

Medicine, Genetics, Obstetrics +13

Limb girdle muscular dystrophy type 2G with myopathic-neurogenic motor unit potentials and a novel muscle image pattern

Ana Cotta, Júlia Filardi Paim, Antonio Lopes da-Cunha-Júnior et al. · BMC Clinical Pathology · 2014 · 36 citations · Full text

Medicine, Neurology, Human Genetics +16

Muscle Protein Alterations in LGMD2I Patients With Different Mutations in the Fukutin-related Protein Gene

Lydia U. Yamamoto, Fernando Janczur Velloso, Luciana Luchesi Quintanilha Fogaça et al. · Journal of Histochemistry & Cytochemistry · 2008 · 22 citations · Full text

Medicine, Genetics, Molecular Genetics +15