Low aerobic capacity in McArdle disease: A role for mitochondrial network impairment? von Villarreal-Salazar, M., Santalla, A., Real-Martínez, A., Nogales-Gadea, G., Valenzuela, P.L., Fiuza-Luces, C., Andreu, A.L., Rodríguez-Aguilera, J.C., Martín, M.A., Arenas, J., Vissing, J., Lucia, A., Krag, T.O., Pinós, T.

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Mitochondrial DNA oxidation and manganese superoxide dismutase activity in peripheral blood mononuclear cells from type 2 diabetic patients von García-Ramírez, M, Francisco, G, García-Arumí, E, Hernández, C, Martínez, R, Andreu, A.L, Simó, R

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P.5.12 A mutation in TNPO3 causes LGMD1F and characteristic nuclear pathology von Kubota, A, Melia, M.J, Ortolano, S, Vilchez, J.J, Gamez, J, Tanji, K, Bonilla, E, Palenzuela, L, Fernandez-Cadenas, I, Pristoupilova, A, Garcia-Arumi, E, Andreu, A.L, Navarro, C, Marti, R, Hirano, M

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Effect of an ambulatory diagnostic and treatment programme in patients with sleep apnoea von ANDREU, A. L, CHINER, E, SANCHO-CHUST, J. N, PASTOR, E, LLOMBART, M, GOMEZ-MERINO, E, SENENT, C, BARBE, F

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Splicing mosaic of the myophosphorylase gene due to a silent mutation in McArdle disease von FERNANDEZ-CADENAS, I, ANDREU, A. L, GAMEZ, J, GONZALO, R, MARTIN, M. A, RUBIO, J. C, ARENAS, J

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Reversion of mtDNA depletion in a patient with TK2 deficiency von VILA, M. R, SEGOVIA-SILVESTRE, T, ANDREU, A. L, GAMEZ, J, MARINA, A, NAINI, A. B, MESEGUER, A, LOMBES, A, BONILLA, E, DIMAURO, S, HIRANO, M

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A novel autosomal dominant limb-girdle muscular dystrophy (LGMD 1F) maps to 7q32.1-32.2 von Palenzuela, L, Andreu, A L, Gàmez, J, Vilà, M R, Kunimatsu, T, Meseguer, A, Cervera, C, Fernandez Cadenas, I, van der Ven, P F M, Nygaard, T G, Bonilla, E, Hirano, M

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McArdle disease: Another systemic low-inflammation disorder? von Lucia, Alejandro, Smith, Lucille, Naidoo, Melissa, González-Freire, Marta, Pérez, Margarita, Rubio, Juan C., Martín, Miguel A., Andreu, A.L., Arenas, Joaquín

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Variable presentation of the clinical phenotype of McArdle's disease in a kindred harbouring a novel compound genotype in the muscle glycogen phosphorylase gene von Paradas, C., Fernandez-Cadenas, I., Gallardo, E., Lligé, D., Arenas, J., Illa, I., Andreu, A.L.

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Autosomal dominant limb-girdle muscular dystrophy : A large kindred with evidence for anticipation von GAMEZ, J, NAVARRO, C, HIRANO, M, CERVERA, C, ANDREU, A. L, FERNANDEZ, J. M, PALENZUELA, L, TEJEIRA, S, FERNANDEZ-HOJAS, R, SCHWARTZ, S, KARADIMAS, C, DIMAURO, S

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Increased muscle nucleoside levels associated with a novel frameshift mutation in the thymidine phosphorylase gene in a Spanish patient with MNGIE von Blazquez, A., Martín, M.A., Lara, M.C., Martí, R., Campos, Y., Cabello, A., Garesse, R., Bautista, J., Andreu, A.L., Arenas, J.

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Acute Pneumonitis and Adult Respiratory Distress Syndrome After Subcutaneous Injection of Liquid Silicone von Pastor, E., Andreu, A.L., Chiner, E.

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Bronchopneumonia Due to Nocardia asteroides in a Man With Chronic Obstructive Pulmonary Disease von Díez-García, M.J., Andreu, A.L., Chiner, E.

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Neumonitis aguda y síndrome de distrés respiratorio del adulto tras inyección subcutánea de silicona líquida von Pastor, E., Andreu, A.L., Chiner, E.

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Description of a New Procedure for Fiberoptic Brochoscopy During Noninvasive Ventilation Through a Nasal Mask in Patients With Acute Rspitatory Failure von Chiner, E., Llombart, M., Signes-Costa, J., Andreu, A.L., Gómez-Merino, E., Pastor, E., Arriero, J.M.

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Bronconeumonía por Nocardia asteroides en paciente con EPOC von Díez-García, M.J., Andreu, A.L., Chiner, E.

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A new mtDNA mutation in the tRNALeu(UUR) gene associated with ocular myopathy von Campos, Y, Gámez, J, Garcı́a, A, Andreu, A.L, Rubio, J.C, Martı́n, M.A, del Hoyo, P, Navarro, C, Cervera, C, Garesse, R, Arenas, J

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Maternally inherited hearing loss in a large kindred with a novel T7511C mutation in the mitochondrial DNA tRNA Ser(UCN) gene von Sue, C.M., Tanji, K., Hadjigeorgiou, G., Andreu, A.L., Nishino, I., Krishna, S., Bruno, C., Hirano, M., Shanske, S., Bonilla, E., Fischel-Ghodsian, N., DiMauro, S., Friedman, R.

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A new mtDNA mutation in the tRNA Leu(UUR) gene associated with ocular myopathy von Campos, Y, Gámez, J, Garcı́a, A, Andreu, A.L, Rubio, J.C, Martı́n, M.A, del Hoyo, P, Navarro, C, Cervera, C, Garesse, R, Arenas, J

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A new mitochondrial DNA mutation (A3288G) in the tRNA Leu(UUR) gene associated with familial myopathy von Hadjigeorgiou, G.M., Kim, S.H., Fischbeck, K.H., Andreu, A.L., Berry, G.T., Bingham, P., Shanske, S., Bonilla, E., DiMauro, S.

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