Familial multiple symmetric lipomatosis associated with the A8344G mutation of mitochondrial DNA von GAMEZ, J, PLAYAN, A, ANDREU, A. L, BRUNO, C, NAVARRO, C, CERVERA, C, ARBOS, M. A, SCHWARTZ, S, ENRIQUEZ, J. A, MONTOYA, J

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Bilateral striatal necrosis associated with a novel mutation in the mitochondrial ND6 gene von Solano, Abelardo, Roig, Manuel, Vives-Bauza, Cristofol, Hernandez-Peña, Jose, Garcia-Arumi, Elena, Playan, Ana, Lopez-Perez, Manuel J., Andreu, Antonio L., Montoya, Julio

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Characterisation of repeat and palindrome elements in patients harbouring single deletions of mitochondrial DNA von Solano, A, Gámez, J, Carod, F J, Pineda, M, Playán, A, López-Gallardo, E, Andreu, A L, Montoya, J

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Uncoupling Protein-1 mRNA Expression in Lipomas from Patients Bearing Pathogenic Mitochondrial DNA Mutations von Vilà, Maya R., Gámez, Josep, Solano, Abelardo, Playán, Ana, Schwartz, Simó, Santorelli, Filippo M., Cervera, Carles, Casali, Carlo, Montoya, Julio, Villarroya, Francesc

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Peripheral neuropathy with ataxia in childhood as a result of the G8363A mutation in mitochondrial DNA von PINEDA, Mercedes, SOLANO, Abelardo, ARTUCH, Rafael, ANDREU, Antonio L, PLAYAN, Ana, VILASECA, Maria A, COLOMER, Jaime, BRIONES, Paz, CASADEMONT, Jordi, MONTOYA, Julio

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Familiar chronic progressive external ophthalmoplegia of mitochondrial origin von Pineda, M, Playán-Ariso, A, Alcaine-Villarroya, M J, Vernet, A M, Serra-Castanera, A, Solano, A, Vilaseca, M A, Artuch, R, López-Pérez, M, Briones-Godino, M P, Andreu, A, Montoya, J

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A single deletion of mitochondrial DNA in a Brazilian patient with chronic progressive external ophthalmoplegia von Carod-Artal, F J, Solano-Palacios, A, Playán-Ariso, A, Viana-Brandi, I, López-Gallardo, E, Andreu, A, López-Pérez, M, Montoya, J

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Multiple Endocrine Involvement in Two Pediatric Patients with Kearns-Sayre Syndrome von Artuch, Rafael, Pavía, Carlos, Playán, Ana, Vilaseca, Maria Antònia, Colomer, Jaume, Valls, Carme, Rissech, Miquel, González, María Antonia, Pou, Adolf, Briones, Paz, Montoya, Julio, Pineda, Mercé

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Oxygen consumption measurement in lymphocytes for the diagnosis of pediatric patients with oxidative phosphorylation diseases von Artuch, Rafael, Colomé, Catrina, Playán, Ana, Alcaine, María J, Briones, Paz, Montoya, Julio, Vilaseca, Maria A, Pineda, Mercé

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De Toni-Debré-Fanconi syndrome due to a palindrome-flanked deletion in mitochondrial DNA von Solano, Abelardo, Russo, Giovanna, Playán, Ana, Parisi, Maria, DiPietro, Massimo, Scuderi, Antonino, Palumbo, Maddalena, Renis, Marcella, López-Pérez, Manuel J, Andreu, Antoni L, Montoya, Julio

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Leigh syndrome resulting from a de novo mitochondrial DNA mutation (T8993G) von Playán, A, Solano-Palacios, A, González de la Rosa, J B, Merino-Arribas, J M, Andreu, A L, López-Pérez, M, Montoya, J

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Diseases of mitochondrial DNA von Montoya, J, Playán, A, Solano, A, Alcaine, M J, López-Pérez, M J, Pérez-Martos, A

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Acute presentation of leukodystrophy due to mitochondrial cytopathology and multiple deletions of mitochondrial DNA von Rábano, J A, Playan, A, Guirado, F, Montoya, J, Baldellou, A, López-Pisón, J

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Mitochondrial encephalomyelitis, lactic acidosis and cerebrovascular accidents (MELAS) in pediatric age with the A3243G mutation in the tRNALeu(UUR) gene of mitochondrial DNA von Coelho-Miranda, L, Playan, A, Artuch, R, Vilaseca, M A, Colomer, J, Briones, P, Coll-Cantí, J, Conill, J, Sans, A, López de Munain, A, Solano, A, Alcaine, M J, Montoya, J, Pineda, M

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Genetic diseases of the mitochondrial DNA in humans von Solano, A, Playán, A, López-Pérez, M J, Montoya, J

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Encefalomiopatía mitocondrial, acidosis láctica y accidentes cerebrovasculares (MELAS) en edad pediátrica con la mutación A3243G en el gen del ARNtLeu(UUR) del ADN mitocondrial von Coelho Miranda, Lucio, Playán, Ana, Artuch Iriberri, Rafael, Vilaseca Buscà, Maria Antònia, Colomer Oferil, Jaume, Briones Godino, Paz, Coll Cantí, Jaume, Conill Ramón, Juan José, Sans Fitó, Anna, López de Munain Arregui, Adolfo, Solano, Abelardo, Alcaine Villarroya, María José, Montoya Villaroya, Julio, Pineda Marfà, Mercè

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Leucodistrofia de presentación aguda por citopatía mitocondrial y deleciones múltiples del ADN mitocondrial von Rábano, J.A., Playán, Ana, Guirado, F., Montoya Villaroya, Julio, Baldellou Vázquez, Antonio, López Pisón, Javier

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Recent advances in genetics of epilepsy. Genetic of mitochondrial epilepsy von Montoya, J, Playán, A, Alcaine, M J, Solano, A, Fernández-Silva, P, Enríquez, J A

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Síndrome de Leigh producido por una mutación de novo T8993G en el ADN mitocondrial von Playán Ariso, Ana, Solano Palacios, Abelardo, González de la Rosa, José Bernardo, Merino Arribas, José Manuel, Andreu Périz, Antoni L., López Pérez, Manuel José, Montoya Villaroya, Julio

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Modernization and optimization of irrigation systems to increase water productivity von Playán, Enrique, Mateos, Luciano

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