Search Results - "García‐Arumí, E."

Influence of Mitochondrial Genetics on the Mitochondrial Toxicity of Linezolid in Blood Cells and Skin Nerve Fibers by 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

“…The antibiotic linezolid is a ribosomal inhibitor with excellent efficacy. Although the administration period has been reduced to 28 days, side effects,…”
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Comparison of different techniques for purification of triamcinolone acetonide suspension for intravitreal use by García-Arumí, J, Boixadera, A, Giralt, J, Martinez-Castillo, V, Gomez-Ulla, F, Corcostegui, B, García-Arumí, E

“…Background: Intravitreal triamcinolone has increasingly been used for the treatment of oedematous and neovascular diseases and purification of triamcinolone…”
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Mitochondrial DNA oxidation and manganese superoxide dismutase activity in peripheral blood mononuclear cells from type 2 diabetic patients by García-Ramírez, M, Francisco, G, García-Arumí, E, Hernández, C, Martínez, R, Andreu, A.L, Simó, R

“…Abstract Aim To investigate the balance between parameters of oxidative stress and antioxidant defences in the mitochondria of peripheral blood mononuclear…”
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Severe late onset mitochondrial myopathy caused by TK2 mutations by Gil, E. Vergés, Bayarri, J. Gascón, Carreño-Gago, L, García-Arumí, E, Plana, M. Olivé

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Prevalence of mitochondrial A3243G mutation in adult type 1 diabetic patients in Catalonia by Francisco, G, Hernández, C, Martínez, R, García-Arumí, E, Andreu, A, Simó, R

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Genetic identification of Spanish civil war victims. The state of the art in Catalonia (Northeastern Spain) by Palomo-Díez, S., Gomes, C., López-Parra, A.M., Baeza-Richer, C., Cuscó, I., Raffone, C., García-Arumí, E., Vinueza-Espinosa, D.C., Santos, C., Montes, N., Rasal, R., Escala, O., Cuellar, J., Subirá, E., Casals, F., Malgosa, A., Tizzano, E., Tartera, E., Domenech, G., Arroyo-Pardo, E.

“…At the end of 2016 and under the initiative and funding of the “Direcció General de Memòria democràtica-Departament de Justícia” (Generalitat of Catalonia), it…”
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Pediatric onset of mitochondrial myopathy due to ANT1 mutation by Martinez-Saez, E, Olive, M, Sanchez-Montañez, A, Gratacos, M, Gran-Piña, F, García-Arumí, E, Paredes, F, Camacho-Soriano, J, Ramón y Cajal, S, Macaya, A, Munell, F

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Muscle magnetic resonance imaging involvement in mitochondrial myopathy due to TK2 deficiency by Sánchez-Montañez, A, Martínez-Sáez, E, de la Banda, M. Gómez García, Julià, N, Quijano-Roy, S, Olivé, M, García-Arumí, E, Gratacós, M, Buendía, J, Delgado, I, Vázquez, E, Roig, M, Munell, F

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Usefulness of short-lived proteins as nutritional indicators surgical patients by LÓPEZ-HELLIN, J., BAENA-FUSTEGUERAS, J.A., SCHWARTZ-RIERA, S., GARCÍA-ARUMÍ, E.

“…Background and aims: Biochemical indicators are used to assess the adequacy of nutritional support given to postoperative patients. However, the metabolic…”
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Effect of oxidative stress on lymphocytes from elderly subjects by García-Arumí, E, Andreu, A L, López-Hellín, J, Schwartz, S

“…1. Oxidative damage has been associated with ageing, but there is no agreement as to whether or not it is produced by a decrease in antioxidant defences with…”
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Identification and biochemical characterization of the novel mutation m.8839G>C in the mitochondrial ATP6 gene associated with NARP syndrome by 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.

“…Mutations in the ATP6 gene are reported to be associated with Leber hereditary optic neuropathy, bilateral striatal necrosis, coronary atherosclerosis risk and…”
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EP.05New POLG mutation causing autosomal dominant PEO, proximal and distal myopathy and respiratory failure by Gonzalez Mera, L., Carreño-Gago, L., Pellisé, A., Paramonov, I., García-Arumí, E., Olivé, M.

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P.305 - Severe late onset mitochondrial myopathy caused by TK2 mutations by Gil, E. Vergés, Bayarri, J. Gascón, Carreño-Gago, L., García-Arumí, E., Plana, M. Olivé

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Nutritional modulation of protein metabolism after gastrointestinal surgery by Lopez Hellin, J, Baena-Fustegueras, J.A, Sabin-Urkia, P, Schwartz-Riera, S, Garcia-Arumi, E

“…Background: The metabolic response to surgery includes alterations in protein metabolism, resulting in a net loss of proteins. Protein hypercatabolism is…”
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Kidney Androgen-Regulated Protein Transgenic Mice Show Hypertension and Renal Alterations Mediated by Oxidative Stress by TORNAVACA, O, PASCUAL, G, LOPEZ-NOVOA, J. M, MESEGUER, A, BARREIRO, M. L, GRANDE, M. T, CARRETERO, A, RIERA, M, GARCIA-ARUMI, E, BARDAJI, B, GONZALEZ-NUNEZ, M, MONTERO, M. A

“…Kidney androgen-regulated protein (KAP), a proximal tubule androgen-regulated gene, codes for a protein of unknown function. To investigate the consequences of…”
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P.306 - Muscle magnetic resonance imaging involvement in mitochondrial myopathy due to TK2 deficiency by Sánchez-Montañez, A., Martínez-Sáez, E., de la Banda, M. Gómez García, Julià, N., Quijano-Roy, S., Olivé, M., García-Arumí, E., Gratacós, M., Buendía, J., Delgado, I., Vázquez, E., Roig, M., Munell, F.

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P.298 - Pediatric onset of mitochondrial myopathy due to ANT1 mutation by Martinez-Saez, E., Olive, M., Sanchez-Montañez, A., Gratacos, M., Gran-Piña, F., García-Arumí, E., Paredes, F., Camacho-Soriano, J., Ramón y Cajal, S., Macaya, A., Munell, F.

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Identification and biochemical characterization of the novel mutation m. 8839G >C in the mitochondrial ATP6 gene associated with NARP syndrome by 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.

“…Mutations in the ATP6 gene are reported to be associated with Leber hereditary optic neuropathy, bilateral striatal necrosis, coronary atherosclerosis risk and…”
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P.5.12 A mutation in TNPO3 causes LGMD1F and characteristic nuclear pathology by 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

“…Limb-girdle muscular dystrophy 1F (LGMD1F) is an autosomal dominant muscular disease affecting a Spanish family. Using whole genome sequencing, we identified a…”
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24 Deep intronic mutations in cystic fibrosis patients detected by next generation sequencing by Fernandez, P, Reyes, K. Loor, Álvarez-Rios, A.I, Arumí, E. Garcia, Chang, P, Culebras, M, de Gracia, J, Gartner, S, Tizzano, E

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