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