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Browsing by Author Artuch, Rafael

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Showing results 1 to 14 of 14
RightsIssue DateTitleAuthor(s)
openAccess6-Jul-20125-Oxoprolinuria in Heterozygous Patients for 5-Oxoprolinase (OPLAH) Missense ChangesCalpena, Eduardo; Casado, Mercedes; Martínez-Rubio, Dolores; Nascimento, Andrés; Colomer, Jaume; Gargallo, Eva; García-Cazorla, Angels; Palau Martínez, Francesc; Artuch, Rafael; Espinós, Carmen
closedAccess20-Mar-2008Analysis of Coenzyme Q10 in muscle and fibroblasts for the diagnosis of CoQ10 deficiency syndromesMontero, Raquel; Sánchez-Alcázar, José Antonio; Briones, Paz; Rodríguez-Hernández, Ángeles; Cordero, Mario D.; Trevisson, Eva; Salviati, Leonardo; Pineda, Mercé; García-Cazorla, Angels; Navas, Plácido, et al
closedAccess2013cblE-type homocystinuria presenting with features of haemolytic-uremic syndrome in the newborn periodPalanca, Daniel; García-Cazorla, Angels; Ortiz, Jessica; Jou, Cristina; Cusí, Victoria; Suñol, Mariona; Toll, Teresa; Pérez, Belén; Ormazabal, Aida; Fowler, Brian, et al
closedAccess2013Clinical, biochemical, molecular and therapeutic aspects of 2 new cases of 2-aminoadipic semialdehyde synthase deficiencyTondo, Mireia; Calpena, Eduardo; Arriola, Gema; Sanz, Paloma; Martorell, Loreto; Ormazabal, Aida; Castejón, Esperanza; Ugarte, Magdalena; Espinos, Carmen; Pérez, Belén, et al
openAccess1-Jan-2009Coenzyme Q deficiency triggers mitochondria degradation by mitophagyRodríguez-Hernández, Ángeles; Cordero, Mario D.; Salviati, Leonardo; Artuch, Rafael; Pineda, Mercé; Briones, Paz; Gómez Izquierdo, Lourdes; Cotán, David; Navas, Plácido; Sánchez-Alcázar, José Antonio
closedAccess2009Coenzyme Q10 deficiencies in neuromuscular diseasesArtuch, Rafael; Salviati, Leonardo; Jackson, Sandra; Navas, Plácido
closedAccess3-Dec-2008Coenzyme Q10 deficiency associated with a mitochondrial DNA depletion syndrome: A case reportMontero, Raquel; Sánchez-Alcázar, José Antonio; Gallardo, M. Esther; Bornstein, Belén; Rivera, Henry; Martín, Miguel A.; Navas, Plácido; Artuch, Rafael
closedAccess13-Apr-2010Coenzyme Q10-responsive ataxia: 2-year-treatment follow-upPineda, Mercé; Aracil, Asunción; O'Callaghan, Mar M.; Más, Ana; Espinos, Carmen; Martínez-Rubio, Dolores; Palau Martínez, Francesc; Navas, Plácido; Briones, Paz; Artuch, Rafael
closedAccess2013Development of the serotonergic cells in murine raphe nuclei and their relations with rhombomeric domainsAlonso, Antonia; Merchán, Paloma; Sandoval, Juan E.; Sánchez-Arroes, Luisa; García-Cazorla, Angels; Artuch, Rafael; Mrtínez de la Torre, Margaret; Puelles, Luis; Ferrán, José Luis
closedAccess18-May-2008Functional characterization of human COQ4, a gene required for Coenzyme Q10 biosynthesisCasarin, Alberto; Jímenez-Ortega, José Carlos; Trevisson, Eva; Pertegato, Vanessa; Doimo, Mara; Ferrero-Gómez, María Lara; Abbadi, Sara; Artuch, Rafael; Quinzii, Catarina; Hirano, Michio, et al
openAccess21-Aug-2012Guiametabolica.org: empowerment through internet tools in inherited metabolic diseasesArmayones, Manuel; Vilaseca, M. A.; Cutillas, Júlia; Fàbrega, Jordi; Fernández, Jorge J.; García, Mei; Egea, Natàlia; Pousada, Modesta; Gómez-Zuñiga, Beni; Pérez-Payarols, Jaume, et al
closedAccess2012Mild Clinical and Biochemical Phenotype in Two Patients with PMM2-CDG (Congenital Disorder of Glycosylation Ia)Casado, Mercedes; O'Callaghan, M.; Montero, R.; Pérez-Cerdá, Celia; Pérez, Belén; Briones, P.; Quintana, E.; Muchart, J.; Aracil, A.; Pineda, M., et al
openAccess2009Mutations in the urocanase gene UROC1 are associated with urocanic aciduriaEspinós, Carmen; Pineda, Mercè; Martínez-Rubio, Dolores; Lupo, Vincenzo; Ormazabal, Aida; Vilaseca, María A.; Spaapen, Leo J. M.; Palau Martínez, Francesc; Artuch, Rafael
closedAccess2012Novel features in the evolution of adenylosuccinate lyase deficiencyPerez-Dueñas, Belén; Sempere, Ángela; Campistol, Jaume; Alonso-Colmenero, Itziar; Díez, María; González, Verónica; Merinero, Begoña; Desviat, Lourdes R.; Artuch, Rafael