Influence of Mitochondrial Genetics on the Mitochondrial Toxicity of Linezolid in Blood Cells and Skin Nerve Fibers
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
Published in Antimicrobial agents and chemotherapy (01.09.2017)
Published in Antimicrobial agents and chemotherapy (01.09.2017)
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Effect of an ambulatory diagnostic and treatment programme in patients with sleep apnoea
ANDREU, A. L, CHINER, E, SANCHO-CHUST, J. N, PASTOR, E, LLOMBART, M, GOMEZ-MERINO, E, SENENT, C, BARBE, F
Published in The European respiratory journal (01.02.2012)
Published in The European respiratory journal (01.02.2012)
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Infusion of platelets transiently reduces nucleoside overload in MNGIE
Lara, M C, Weiss, B, Illa, I, Madoz, P, Massuet, L, Andreu, A L, Valentino, M L, Anikster, Y, Hirano, M, Martí, R
Published in Neurology (24.10.2006)
Published in Neurology (24.10.2006)
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Hematopoietic gene therapy restores thymidine phosphorylase activity in a cell culture and a murine model of MNGIE
Torres-Torronteras, J, Gómez, A, Eixarch, H, Palenzuela, L, Pizzorno, G, Hirano, M, Andreu, A L, Barquinero, J, Martí, R
Published in Gene therapy (01.08.2011)
Published in Gene therapy (01.08.2011)
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Identification and biochemical characterization of the novel mutation m.8839G>C in the mitochondrial ATP6 gene associated with NARP syndrome
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.
Published in Genes, brain and behavior (01.11.2013)
Published in Genes, brain and behavior (01.11.2013)
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NARP syndrome in a patient harbouring an insertion in the MT-ATP6 gene that results in a truncated protein
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
Published in Journal of medical genetics (01.01.2009)
Published in Journal of medical genetics (01.01.2009)
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Exercise Intolerance Due to Mutations in the Cytochrome b Gene of Mitochondrial DNA
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
Published in The New England journal of medicine (30.09.1999)
Published in The New England journal of medicine (30.09.1999)
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Novel mutations in patients with McArdle disease by analysis of skeletal muscle mRNA
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
Published in Journal of medical genetics (01.03.2009)
Published in Journal of medical genetics (01.03.2009)
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Splicing mosaic of the myophosphorylase gene due to a silent mutation in McArdle disease
Fernandez-Cadenas, I, Andreu, A L, Gamez, J, Gonzalo, R, Martín, M A, Rubio, J C, Arenas, J
Published in Neurology (25.11.2003)
Published in Neurology (25.11.2003)
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Mitochondrial DNA oxidation and manganese superoxide dismutase activity in peripheral blood mononuclear cells from type 2 diabetic patients
García-Ramírez, M, Francisco, G, García-Arumí, E, Hernández, C, Martínez, R, Andreu, A.L, Simó, R
Published in Diabetes & metabolism (01.04.2008)
Published in Diabetes & metabolism (01.04.2008)
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Mitochondrial neurogastrointestinal encephalomyopathy: An autosomal recessive disorder due to thymidine phosphorylase mutations
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
Published in Annals of neurology (01.06.2000)
Published in Annals of neurology (01.06.2000)
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Reversion of mtDNA depletion in a patient with TK2 deficiency
Vilà, M R, Segovia-Silvestre, T, Gámez, J, Marina, A, Naini, A B, Meseguer, A, Lombès, A, Bonilla, E, DiMauro, S, Hirano, M, Andreu, A L
Published in Neurology (08.04.2003)
Published in Neurology (08.04.2003)
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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
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
Published in Neurology (10.06.1999)
Published in Neurology (10.06.1999)
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Exercise intolerance due to a nonsense mutation in the mtDNA ND4 gene
Andreu, A. L., Tanji, K., Bruno, C., Hadjigeorgiou, G. M., Sue, C. M., Jay, C., Ohnishi, T., Shanske, S., Bonilla, E., DiMauro, S.
Published in Annals of neurology (01.06.1999)
Published in Annals of neurology (01.06.1999)
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A missense mutation in the mitochondrial cytochrome b gene in a revisited case with histiocytoid cardiomyopathy
ANDREU, A. L, CHECCARELLI, N, IWATA, S, SHANSKE, S, DIMAURO, S
Published in Pediatric research (01.09.2000)
Published in Pediatric research (01.09.2000)
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A nonsense mutation (G15059A) in the cytochrome b gene in a patient with exercise intolerance and myoglobinuria
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.
Published in Annals of neurology (01.01.1999)
Published in Annals of neurology (01.01.1999)
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Lack of gastrointestinal symptoms in a 60-year-old patient with MNGIE
Martín, M A, Blázquez, A, Martí, R, Bautista, J, Lara, M C, Cabello, A, Campos, Y, Belda, O, Andreu, A L, Arenas, J
Published in Neurology (26.10.2004)
Published in Neurology (26.10.2004)
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McArdle disease: Another systemic low-inflammation disorder?
Lucia, Alejandro, Smith, Lucille, Naidoo, Melissa, González-Freire, Marta, Pérez, Margarita, Rubio, Juan C., Martín, Miguel A., Andreu, A.L., Arenas, Joaquín
Published in Neuroscience letters (31.01.2008)
Published in Neuroscience letters (31.01.2008)
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Mobilisation of mesenchymal cells into blood in response to skeletal muscle injury
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
Published in British journal of sports medicine (01.08.2006)
Published in British journal of sports medicine (01.08.2006)
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Familial multiple symmetric lipomatosis associated with the A8344G mutation of mitochondrial DNA
Gámez, J, Playán, A, Andreu, A L, Bruno, C, Navarro, C, Cervera, C, Arbós, M A, Schwartz, S, Enriquez, J A, Montoya, J
Published in Neurology (01.07.1998)
Published in Neurology (01.07.1998)
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