Zobrazeno 1 - 10
of 55
pro vyhledávání: '"Mayana Zatz"'
Autor:
G. Diane Shelton, Katie M. Minor, Natassia M. Vieira, Louis M. Kunkel, Steven G. Friedenberg, Jonah N. Cullen, Ling T. Guo, Mayana Zatz, James R. Mickelson
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Neuromuscular disorders : NMD, vol 32, iss 10
Universidade de São Paulo (USP)
instacron:USP
Neuromuscular disorders : NMD, vol 32, iss 10
A form of dystrophinopathy with mild or subclinical neuromuscular signs has been previously reported in a family of Labrador retrievers. Markedly and persistently elevated creatine kinase activity was first noted at 6 months of age. Skeletal muscle b
Autor:
Juliana Gurgel-Giannetti, Mayana Zatz, G. Sampaio, J. Wang, Mariz Vainzof, Marilia O. Scliar, Lucas Santos Souza
Publikováno v:
Neuromuscular Disorders. 30:S91-S92
Autor:
Giuliana Castello Coatti, Mayana Zatz, E. Cangussu, F. Vieira Loures, B. Ghirotto, Ernesto Goulart, Héctor Bueno, Antonio Condino-Neto, Elia Garcia Caldini
Publikováno v:
Neuromuscular Disorders. 27:S192-S193
Autor:
T. Valladares, R. Pavanello, D. Rüdiger, Helga Cristina Almeida da Silva, E. Padovan, L. Dantas, M. Naccache, A. Mouzat, D. Castro, E. Macedo, T. Genesini, L. Lise, H. Andrade, J. Forbes, A. Bogochvol, Mayana Zatz, F. Fonseca
Publikováno v:
Neuromuscular Disorders. 27:S130
Autor:
Mayana Zatz, Maria Rita Passos-Bueno, R. Pavanello, A Cerqueira, Sérgio Russo Matioli, M.M.O Tonini
Publikováno v:
Neuromuscular Disorders. 14:33-38
Facioscapulohumeral muscular dystrophy is an autosomal dominant muscle disorder, mapped to 4q35. It is characterized by remarkable inter- and intrafamilial clinical variability ranging from severe phenotype to asymptomatic carriers. The aim of the pr
Autor:
J. Forbes, Mayana Zatz, R. Pavanello, D. Rüdiger, M. Vianna, L. Lise, T. Genesini, A. Mouzat, H. Andrade, L. Fachinetto, E. Macedo, C. Riolfi, G. Achôa
Publikováno v:
Neuromuscular Disorders. 25:S241-S242
Autor:
Juliana Gurgel-Giannetti, Mayana Zatz, Marie Louise Bang, Moacir A.T Fireman, Umbertina Conti Reed, Katarina Pelin, Siegfried Labeit, Mary S. Carvalho, Kati Donner, Edmar Zanoteli, Acary Souza Bulle Oliveira, Mariz Vainzof, Carina Wallgren-Pettersson, Sueli K.N. Marie
Publikováno v:
University of Helsinki
Nemaline myopathy is a structural congenital myopathy which may show both autosomal dominant and autosomal recessive inheritance patterns. Mutations in three different genes have been identified as the cause of nemaline myopathy: the gene for slow al
Autor:
Juliana Gurgel-Giannetti, M. Machado, Mayana Zatz, Mariz Vainzof, Monize Lazar, Acary Sousa Bulle Oliveira, W. Tavares, Guilherme L. Yamamoto, R. Pavanello
Publikováno v:
Neuromuscular Disorders. 26:S132
Autor:
J. Marshall, Matthew S. Alexander, Ingegerd Elvers, Kerstin Lindblad-Toh, Mayana Zatz, A. Assoni, Natássia M. Vieira, Sergio Verjovski-Almeida, Alal Eran, Louis M. Kunkel
Publikováno v:
Neuromuscular Disorders. 26:S156
Autor:
J. Forbes, T. Valladares, H. Andrade, R. Pavanello, F. Fonseca, L. Lagonegro, A. Mouzat, E. Padovan, Mayana Zatz, M. Naccache, E. Macedo, H. Araujo, D. Rüdiger, T. Genesini, L. Lise
Publikováno v:
Neuromuscular Disorders. 26:S208