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Issue DateTitleAuthor(s)
16-Aug-2001¿Existe correlación entre la enfermedad de Alzheimer y defectos en el ADN mitocondrial?Rodríguez Santiago, Benjamín; Casademont i Pou, Jordi; Nunes Martínez, Virginia
23-May-2019Metabolic, mitochondrial, renal and hepatic safety of enfuvirtide and raltegravir antiretroviral administration: Randomized crossover clinical trial in healthy volunteersBarroso, Sergio; Morén Núñez, Constanza; González-Segura, Àlex; Riba, Neus; Arnaiz Gargallo, Juan Alberto; Manriquez, Marcela; Santana, Gemina; Blanco, José L.; Larousse, María; Loncá, Montserrat; Lazzari, Elisa de; Llopis Pérez, Jaime; Mallolas Masferrer, Josep; Miró, Òscar; Carné Cladellas, Xavier; Gatell, José M.; Garrabou Tornos, Glòria; Martínez, Esteban
1-Feb-2022Comprehensive summary of mitochondrial DNA alterations in the postmortem human brain: A systematic reviewValiente Pallejà, Alba; Tortajada, Juan; Bulduk, Bengisu K.; Vilella, Elisabet; Garrabou Tornos, Glòria; Muntané, Gerard; Martorell, Lourdes
8-Apr-2022Multicentric Standardization of protocols for the diagnosis of human mitochondrial respiratory chain defectsBujan, Nuria; Morén Núñez, Constanza; García-García, Francesc Josep; Blázquez, Alberto; Carnicer, Clara; Cortés, Ana Belén; González, Cristina; López-Gallardo, Ester; Lozano Garcia, Ester; Moliner, Sonia; Gort, Laura; Tobías, Ester; Delmiro, Aitor; Martín, Miguel A.; Fernández-Moreno, Miguel Ángel; Ruiz-Pesini, Eduardo; Garcia-Arumí, Elena; Rodríguez-Aguilera Juan Carlos; Garrabou Tornos, Glòria
24-Nov-2021Telomere Length but Not Mitochondrial DNA Copy Number Is Altered in Both Young and Old COPDCasas Recasens, Sandra; Mendoza, Núria; López Giraldo, Alejandra; García, Tamara; Cosío, Borja G.; Pascual-Guardia, Sergi; Acosta Castro, Ady; Borras Santos, Alicia; Gea Guiral, Joaquim; Garrabou Tornos, Glòria; Agustí García-Navarro, Àlvar; Faner, Rosa
1-Feb-2014Transcriptomic profiling of TK2 deficient human skeletal muscle suggests a role for the p53 signalling pathway and identifies growth and differentiation factor-15 as a potential novel biomarker for mitochondrial myopathiesKalko, Susana; Paco Mercader, Sonia; Jou, Cristina; Rodríguez, María Angeles; Meznaric, Marija; Rogac, Mihael; Jekovec-Vrhovsek, Maja; Sciacco, Monica; Moggio, Maurizio; Fagiolari, Gigliola; De Paepe, Boel; De Meirleir, Linda; Ferrer, Isidro (Ferrer Abizanda); Roig Quilis, Manuel; Munell Casadesús, Francina; Montoya, Julio; López Gallardo, Ester; Ruiz Pesini, Eduardo; Artuch Iriberri, Rafael; Montero Sánchez, Raquel; Torner Rubies, Ferran; Nascimento, Andrés; Ortez, Carlos Ignacio; Colomer Oferil, Jaume; Jiménez Mallebrera, Cecilia
1999Alteracions del DNA mitocondrial implicades en patologia HumanaNunes Martínez, Virginia; Gómez Zaera, Montse; Casademont i Pou, Jordi
23-Feb-2022Two Sisters with Kallmann Syndrome, Gonadal Dysgenesis, and Multiple Neuromuscular and Endocrine Disorders: Report of Two Cases with Description of an Unusual AssociationCamacho, Marta; Castelo-Branco Flores, Camil