Joaquin Arenas - Dissemin

Papers authored by Joaquin Arenas

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2010 Mari Carmen Gil Borlado, Mari Carmen Gil Borlado, David Moreno Lastres, David Moreno Lastres, Maritza Gonzalez Hoyuela, Maria Moran, Alberto Blazquez, Rosa Pello, Lorena Marin Buera, Lorena Marin Buera, Toni Gabaldon, Juan Jose Garcia Peñas, Juan Jose Garcia Peñas, Miguel A. Martín, Joaquin Arenas

and 1 other authors

Impact of the Mitochondrial Genetic Background in Complex III Deficiency

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Dale E. Rae

, Timothy D. Noakes, Alejandro F. San Juan, Margarita Pérez, Gisela Nogales-Gadea, Jonatan R. Ruiz, María Morán, Miguel A. Martín, Antoni L. Andreu, Joaquín Arenas

, Alejandro Lucia

Excessive skeletal muscle recruitment during strenuous exercise in McArdle patients

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María Morán, Lorena Marín-Buera, M. Carmen Gil Borlado, Henry Rivera, Alberto Blázquez, Sara Seneca, María Vázquez-López, Joaquín Arenas

, Miguel A. Martín, Cristina Ugalde

Cellular Pathophysiological Consequences of BCS1L Mutations in Mitochondrial Complex III Enzyme Deficiency

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Henry Rivera, Begoña Merinero, Mercedes Martinez-Pardo, Ignacio Arroyo, Pedro Ruiz-Sala, Belen Bornstein, Clara Serra-Suhe, Esther Gallardo, Ramon Marti, Maria J. Moran, Cristina Ugalde

, Luis A. Perez Jurado, Antoni L. Andreu, Rafael Garesse, Magdalena Ugarte and 2 other authors

Marked mitochondrial DNA depletion associated with a novel SUCLG1 gene mutation resulting in lethal neonatal acidosis, multi-organ failure, and interrupted aortic arch

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M. Morán, H. Rivera, M. Sánchez Aragó, A. Blázquez, B. Merinero, C. Ugalde

, J. Arenas

, J. M. Cuezva, M. A. Martín

Mitochondrial bioenergetics and dynamics interplay in complex I-deficient fibroblasts

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F. Gomez-Gallego, Félix Gómez Gallego, Jonatan R. Ruiz, Amaya Buxens, Signe Altmäe, Marta Artieda, Catalina Santiago Dorrego, Marta González-Freire, Zoraida Verde Rello, David Arteta, Antonio Martínez, Diego Tejedor, José I. Lao, Joaquín Arenas

, Alejandro Lucía Mulas

Are elite endurance athletes genetically predisposed to lower disease risk?

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2009 M. Carmen Gil-Borlado, Maritza González-Hoyuela, Alberto Blázquez, M. Teresa García-Silva, Toni Gabaldón, Javier Manzanares, Julia Vara, Miguel A. Martín, Sara Seneca, Joaquín Arenas

, Cristina Ugalde

Pathogenic mutations in the 5′ untranslated region of BCS1L mRNA in mitochondrial complex III deficiency

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Margarita Pérez, Jonatan R. Ruiz, María Fernández Del Valle, Gisela Nogales-Gadea, Antoni L. Andreu, Joaquín Arenas

, Alejandro Lucía

The second wind phenomenon in very young McArdle's patients

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Alberto Munoz, Fernando Mateos, Rogelio Simon, Elena Martin-Hernandez, Ana Camacho, Paloma Ferrando, Joaquin Arenas

, Miguel Martin

Mitochondrial Encephalomyopathies in Children. Part II: Advanced MR Tools and the Importance for its Early Recognition in the Acute Clinical Setting

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Alberto Munoz, Fernando Mateos, Rogelio Simon, Elena Martin-Hernandez, Ana Camacho, Paloma Ferrando, Joaquin Arenas

, Miguel Martin

Mitochondrial Encephalomyopathies in Children. Part I: Conventional MR Imaging Findings

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Manuel Castro-Gago, Manuel Oscar Blanco-Barca, Carmen Gómez-Lado, Jesús Eirís-Puñal, Yolanda Campos-González, Joaquín Arenas-Barbero

Respiratory chain complex I deficiency in an infant with Ohtahara syndrome

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P. Juffer, R. Furrer, M. González-Freire, C. Santiago, Z. Verde, L. Serratosa, F. Morate, J. Rubio, M. Martin, J. Ruiz, J. Arenas

, F. Gómez-Gallego, A. Lucia

Genotype Distributions in Top-level Soccer Players: A Role forACE?

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Marta González-Freire, Catalina Santiago, Félix Gómez-Gallego, Margarita Pérez, Carl Foster, Joaquín Arenas

, Alejandro Lucia

Does the K153R variant of the myostatin gene influence the clinical presentation of women with McArdle disease?

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I. Rego, M. Fernández-Moreno

, C. Fernández-López, J. J. Gómez-Reino, A. González, J. Arenas

, F. J. Blanco

Role of European mitochondrial DNA haplogroups in the prevalence of hip osteoarthritis in Galicia, Northern Spain

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Alberto Blázquez, Mari Carmen Gil-Borlado, María Morán, Alfonso Verdú, María Rosario Cazorla-Calleja, Miguel A. Martín, Joaquín Arenas

, Cristina Ugalde

Infantile mitochondrial encephalomyopathy with unusual phenotype caused by a novel BCS1L mutation in an isolated complex III-deficient patient

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J. Arpa, Y. Campos, M. Gutiérrez-Molina, A. Cruz-Martinez, J. Arenas

, A. B. Caminero, F. Palomo, C. Morales, P. Barreiro

Benign mitochondrial myopathy with decreased succinate cytochrome C reductase activity

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J. Arpa, Y. Campos, M. Gutiérrez-Molina, M.-A. Martin-Casanueva, A. Cruz-Martínez, M.-C. Pérez-Conde, R. López-Pajares, M.-C. Morales, J. Tatay, T. Lacasa, P. Barreiro, J. Arenas

Gene dosage effect in one family with myoclonic epilepsy and ragged-red fibers (MERRF)

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J. A. Molina, F. J. Jiménez-Jiménez, J. A. Navarro, C. Vargas, P. Gómez, J. Benito-León, M. Ortí-Pareja, E. Cisneros, J. Arenas

Cerebrospinal fluid nitrate levels in patients with Parkinson's disease

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Cristina Ugalde

, María Morán, Alberto Blázquez, Joaquín Arenas

, Miguel A. Martín

Mitochondrial Disorders Due to Nuclear OXPHOS Gene Defects

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This paper was not found in any repository; the policy of its publisher is unknown or unclear.

Ines Garcia-Consuegra, J. C. Rubio, G. Nogales-Gadea, J. Bautista, S. Jimenez, A. Cabello, A. Lucia

, A. L. Andreu, J. Arenas

, M. A. Martin

Novel human pathological mutations. Gene symbol: PYGM. Disease: McArdle disease

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Papers authored by Joaquin Arenas