AAAAAA

   
Results: 1-6 |
Results: 6

Authors: Gurgel-Giannetti, J Reed, U Bang, ML Pelin, K Donner, K Marie, SK Carvalho, M Fireman, MAT Zanoteli, E Oliveira, ASB Zatz, M Wallgren-Pettersson, C Labeit, S Vainzof, M
Citation: J. Gurgel-giannetti et al., Nebulin expression in patients with nemaline myopathy, NEUROMUSC D, 11(2), 2001, pp. 154-162

Authors: Nitrini, R Mendonca, RA Huang, N LeBlanc, A Livramento, JA Marie, SK
Citation: R. Nitrini et al., Diffusion-weighted MRI in two cases of familial Creutzfeldt-Jakob disease, J NEUR SCI, 184(2), 2001, pp. 163-167

Authors: Kim, CA Passos-Bueno, MR Marie, SK Cerqueira, A Conti, U Marques-Dias, MJ Gonzalez, CH Zatz, M
Citation: Ca. Kim et al., Clinical and molecular analysis of spinal muscular atrophy in Brazilian patients, GENET MOL B, 22(4), 1999, pp. 487-492

Authors: Vainzof, M Moreira, ES Ferraz, G Passos-Bueno, MR Marie, SK Zatz, M
Citation: M. Vainzof et al., Further evidence for the organisation of the four sarcoglycans proteins within the dystrophin-glycoprotein complex, EUR J HUM G, 7(2), 1999, pp. 251-254

Authors: Reed, UC Tsanaclis, AMC Vainzof, M Marie, SK Carvalho, MS Roizenblatt, J Pedreira, CC Diament, A Levy, JA
Citation: Uc. Reed et al., Merosin-positive congenital muscular dystrophy in two siblings with cataract and slight mental retardation, BRAIN DEVEL, 21(4), 1999, pp. 274-278

Authors: Vainzof, M Passos-Bueno, MR Pavanello, RCM Marie, SK Oliveira, ASB Zatz, M
Citation: M. Vainzof et al., Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the Brazilian population, J NEUR SCI, 164(1), 1999, pp. 44-49
Risultati: 1-6 |