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Results: 1-4 |
Results: 4

Authors: Martin, MA Rubio, JC Buchbinder, J Fernandez-Hojas, R del Hoyo, P Teijeira, S Gamez, J Navarro, C Fernandez, JM Cabello, A Campos, Y Cervera, C Culebras, JM Andreu, AL Fletterick, R Arenas, J
Citation: Ma. Martin et al., Molecular heterogeneity of myophosphorylase deficiency (McArdle's disease): A genotype-phenotype correlation study, ANN NEUROL, 50(5), 2001, pp. 574-581

Authors: Calvo, F Teijeira, S Fernandez, JM Teijeiro, A Fernandez-Hojas, R Fernandez-Lopez, XA Martin, E Navarro, C
Citation: F. Calvo et al., Evaluation of heart involvement in gamma-sarcoglycanopathy (LGMD2C). A study of ten patients, NEUROMUSC D, 10(8), 2000, pp. 560-566

Authors: Fernandez, R Navarro, C Andreu, AL Bruno, C Shanske, S Gamez, J Teijeira, S Hernandez, I Teijeiro, A Fernandez, JM Musumeci, O DiMauro, S
Citation: R. Fernandez et al., A novel missense mutation (W797R) in the myophosphorylase gene in Spanish patients with McArdle disease, ARCH NEUROL, 57(2), 2000, pp. 217-219

Authors: Fernandez, R Fernandez, JM Cervera, C Teijeira, S Teijeiro, A Dominguez, C Navarro, C
Citation: R. Fernandez et al., Adult glycogenosis II with paracrystalline mitochondrial inclusions and Hirano bodies in skeletal muscle, NEUROMUSC D, 9(3), 1999, pp. 136-143
Risultati: 1-4 |