Influence of Mitochondrial Genetics on the Mitochondrial Toxicity of Linezolid in Blood Cells and Skin Nerve Fibers von Garrabou, G, Soriano, À, Pinós, T, Casanova-Mollà, J, Pacheu-Grau, D, Morén, C, García-Arumí, E, Morales, M, Ruiz-Pesini, E, Catalán-Garcia, M, Milisenda, J C, Lozano, E, Andreu, A L, Montoya, J, Mensa, J, Cardellach, F

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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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Hematopoietic gene therapy restores thymidine phosphorylase activity in a cell culture and a murine model of MNGIE von Torres-Torronteras, J, Gómez, A, Eixarch, H, Palenzuela, L, Pizzorno, G, Hirano, M, Andreu, A L, Barquinero, J, Martí, R

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Infusion of platelets transiently reduces nucleoside overload in MNGIE von LARA, M. C, WEISS, B, ILLA, I, MADOZ, P, MASSUET, L, ANDREU, A. L, VALENTINO, M. L, ANIKSTER, Y, HIRANO, M, MARTI, R

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Identification and biochemical characterization of the novel mutation m.8839G>C in the mitochondrial ATP6 gene associated with NARP syndrome von Blanco‐Grau, A., Bonaventura‐Ibars, I., Coll‐Cantí, J., Melià, M. J., Martinez, R., Martínez‐Gallo, M., Andreu, A. L., Pinós, T., García‐Arumí, E.

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Exercise Intolerance Due to Mutations in the Cytochrome b Gene of Mitochondrial DNA von Andreu, Antoni L, Hanna, Michael G, Reichmann, Heinz, Bruno, Claudio, Penn, Audrey S, Tanji, Kurenai, Pallotti, Francesco, Iwata, So, Iwata, Momi, Bonilla, Eduardo, Lach, Boleslaw, Morgan-Hughes, John, Shanske, Sara, Sue, Carolyn M, Pulkes, Teeratorn, Siddiqui, Asra, Clark, John B, Land, John, Schaefer, Jochen, DiMauro, Salvatore

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NARP syndrome in a patient harbouring an insertion in the MT-ATP6 gene that results in a truncated protein von López-Gallardo, E, Solano, A, Herrero-Martín, M D, Martínez-Romero, Í, Castaño-Pérez, M D, Andreu, A L, Herrera, A, López-Pérez, M J, Ruiz-Pesini, E, Montoya, J

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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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Mitochondrial neurogastrointestinal encephalomyopathy: An autosomal recessive disorder due to thymidine phosphorylase mutations von Nishino, Ichizo, Spinazzola, Antonella, Papadimitriou, Alexandros, Hammans, Simon, Steiner, Israel, Hahn, Cecil D., Connolly, Anne M., Verloes, Alain, Guimarães, João, Maillard, Ivan, Hamano, Hitoshi, Donati, M. Alice, Semrad, Carol E., Russell, James A., Andreu, Antonio L., Hadjigeorgiou, Giorgos M., Vu, Tuan H., Tadesse, Saba, Nygaard, Torbjoern G., Nonaka, Ikuya, Hirano, Ikuo, Bonilla, Eduardo, Rowland, Lewis P., DiMauro, Salvatore, Hirano, Michio

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Novel mutations in patients with McArdle disease by analysis of skeletal muscle mRNA von García-Consuegra, I, Rubio, J C, Nogales-Gadea, G, Bautista, J, Jiménez, S, Cabello, A, Lucía, A, Andreu, A L, Arenas, J, Martin, M A

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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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A missense mutation in the mitochondrial cytochrome b gene in a revisited case with histiocytoid cardiomyopathy von ANDREU, A. L, CHECCARELLI, N, IWATA, S, SHANSKE, S, DIMAURO, S

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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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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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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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Exercise intolerance due to a nonsense mutation in the mtDNA ND4 gene von Andreu, A. L., Tanji, K., Bruno, C., Hadjigeorgiou, G. M., Sue, C. M., Jay, C., Ohnishi, T., Shanske, S., Bonilla, E., DiMauro, S.

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A Stop-Codon Mutation in the Human mtDNA Cytochrome c Oxidase I Gene Disrupts the Functional Structure of Complex IV von Bruno, Claudio, Martinuzzi, Andrea, Tang, Yingying, Andreu, Antoni L., Pallotti, Francesco, Bonilla, Eduardo, Shanske, Sara, Fu, Jin, Sue, Carolyn M., Angelini, Corrado, DiMauro, Salvatore, Manfredi, Giovanni

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Mobilisation of mesenchymal cells into blood in response to skeletal muscle injury von Ramírez, M, Lucia, A, Gómez-Gallego, F, Esteve-Lanao, J, Pérez-Martínez, A, Foster, C, Andreu, A L, Martin, M A, Madero, L, Arenas, J, García-Castro, J

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A nonsense mutation (G15059A) in the cytochrome b gene in a patient with exercise intolerance and myoglobinuria von Andreu, A. L., Bruno, C., Dunne, T. C., Tanji, K., Shanske, S., Sue, C. M., Krishna, S., Hadjigeorgiou, G. M., Shtilbans, A., Bonilla, E., DiMauro, S.

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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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