Animal Models for Genetic Neuromuscular Diseases by Vainzof, Mariz, Ayub-Guerrieri, Danielle, Onofre, Paula C. G., Martins, Poliana C. M., Lopes, Vanessa F., Zilberztajn, Dinorah, Maia, Lucas S., Sell, Karen, Yamamoto, Lydia U.

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Limb girdle muscular dystrophy type 2G with myopathic-neurogenic motor unit potentials and a novel muscle image pattern by Cotta, Ana, Paim, Julia Filardi, da-Cunha-Junior, Antonio Lopes, Neto, Rafael Xavier, Nunes, Simone Vilela, Navarro, Monica Magalhaes, Valicek, Jaquelin, Carvalho, Elmano, Yamamoto, Lydia U, Almeida, Camila F, Braz, Shelida Vasconcelos, Takata, Reinaldo Issao, Vainzof, Mariz

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Thomsen or Becker myotonia? A novel autosomal recessive nonsense mutation in the CLCN1 gene associated with a mild phenotype by Gurgel‐Giannetti, Juliana, Senkevics, Adriano S., Zilbersztajn‐Gotlieb, Dinorah, Yamamoto, Lydia U., Muniz, Viviane P., Pavanello, Rita C.M., Oliveira, Acary B., ZATZ, Mayana, Vainzof, Mariz

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Silent polymorphisms in the RYR1 gene do not modify the phenotype of the p.4898 I>T pathogenic mutation in central core disease: a case report by Cuperman, Thais, Fernandes, Stephanie A, Lourenço, Naila C V, Yamamoto, Lydia U, Silva, Helga C A, Pavanello, Rita C M, Yamamoto, Guilherme L, Zatz, Mayana, Oliveira, Acary S B, Vainzof, Mariz

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Muscle Protein Alterations in LGMD2I Patients With Different Mutations in the Fukutin-related Protein Gene by Yamamoto, Lydia U, Velloso, Fernando J, Lima, Bruno L, Fogaca, Luciana L.Q, de Paula, Flavia, Vieira, Natassia M, Zatz, Mayana, Vainzof, Mariz

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Genetic variability in the myostatin gene does not explain the muscle hypertrophy and clinical penetrance in myotonia congenita by Muniz, Viviane P., Senkevics, Adriano S., Zilbersztajn, Dinorah, Gurgel-Giannetti, Juliana, Silva, Helga C., Yamamoto, Lydia U., Pavanello, Rita C.M., Pearson, Peter L., Zatz, Mayana, Vainzof, Mariz

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Silent polymorphisms in the RYR1 gene do not modify the phenotype of the p.4898 IT pathogenic mutation in central core disease: a case report by Cuperman, Thais, Fernandes, Stephanie A, Lourenço, Naila CV, Yamamoto, Lydia U, Silva, Helga CA, Pavanello, Rita CM, Yamamoto, Guilherme L, Zatz, Mayana, Oliveira, Acary SB, Vainzof, Mariz

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Prenatal diagnosis in laminin α2 chain (merosin)-deficient congenital muscular dystrophy: A collective experience of five international centers by Vainzof, Mariz, Richard, Pascale, Herrmann, Ralf, Jimenez-Mallebrera, Cecilia, Talim, Beril, Yamamoto, Lydia U., Ledeuil, Céline, Mein, Rachael, Abbs, Stephen, Brockington, Martin, Romero, Norma B., Zatz, Mayana, Topaloglu, Haluk, Voit, Thomas, Sewry, Caroline, Muntoni, Francesco, Guicheney, Pascale, Tomé, Fernando M.S.

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Prenatal diagnosis in laminin alpha2 chain (merosin)-deficient congenital muscular dystrophy: a collective experience of five international centers by Vainzof, Mariz, Richard, Pascale, Herrmann, Ralf, Jimenez-Mallebrera, Cecilia, Talim, Beril, Yamamoto, Lydia U, Ledeuil, Céline, Mein, Rachael, Abbs, Stephen, Brockington, Martin, Romero, Norma B, Zatz, Mayana, Topaloglu, Haluk, Voit, Thomas, Sewry, Caroline, Muntoni, Francesco, Guicheney, Pascale, Tomé, Fernando M S

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Limb girdle muscular dystrophy type 2G with myopathic-neurogenic motor unit potentials and a novel muscle image pattern by Cotta, Ana, Paim, Julia Filardi, da-Cunha-Junior, Antonio Lopes, Neto, Rafael Xavier, Nunes, Simone Vilela, Navarro, Monica Magalhaes, Valicek, Jaquelin, Carvalho, Elmano, Yamamoto, Lydia U, Almeida, Camila F, Braz, Shelida Vasconcelos, Takata, Reinaldo Issao, Vainzof, Mariz

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Thomsen or Becker myotonia? A novel autosomal recessive nonsense mutation in the CLCN1 gene associated with a mild phenotype by Gurgel-Giannetti, Juliana, Senkevics, Adriano S., Zilbersztajn-Gotlieb, Dinorah, Yamamoto, Lydia U., Muniz, Viviane P., Pavanello, Rita C.M., Oliveira, Acary B., ZATZ, Mayana, Vainzof, Mariz

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