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Browsing by Author Campos, Yolanda

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Showing results 1 to 9 of 9
RightsPreviewIssue DateTitleAuthor(s)Type
closedAccessaccesoRestringido.pdf.jpg2006Association of novel POLG mutations and multiple mitochondrial DNA deletions with variable clinical phenotypes in a Spanish populationBlázquez, Alberto; Bornstein, Belén ; Campos, Yolanda; Fernández-Moreno, Miguel Ángel ; Garesse, Rafael ; Arenas, Joaquín; Martín, Miguel A.artículo
closedAccessaccesoRestringido.pdf.jpg2001Early onset multisystem mitochondrial disorder caused by a nonsense mutation in the mitochondrial DNA Cytochrome C oxidase II geneCampos, Yolanda; Fernández-Moreno, Miguel Ángel ; Martín, Miguel A.; Bornstein, Belén ; Garesse, Rafael ; Arenas, Joaquínartículo
closedAccessaccesoRestringido.pdf.jpg2005Increased muscle nucleoside levels associated with a novel frameshift mutation in the thymidine phosphorylase gene in a Spanish patient with MNGIEBlázquez, Alberto; Martín, Miguel A.; Campos, Yolanda; Garesse, Rafael ; Bautista, José M.; Arenas, Joaquínartículo
closedAccessaccesoRestringido.pdf.jpg2005Leigh syndrome associated with mitochondrial complex I deficiency due to a novel mutation in the NDUFS1 geneMartín, Miguel A.; Garesse, Rafael ; Campos, Yolanda; Arenas, Joaquínartículo
closedAccessaccesoRestringido.pdf.jpg2007Mild ocular myopathy associated with a novel mutation in mitochondrial twinkle helicaseRivera, Henry; Blázquez, Alberto; Campos, Yolanda; Bornstein, Belén ; Garesse, Rafael ; Arenas, Joaquín; Martín, Miguel A.artículo
closedAccessaccesoRestringido.pdf.jpg2001Mitochondrial dysfunction associated with a mutation in the Notch3 gene in a CADASIL familyBornstein, Belén ; Fernández-Moreno, Miguel Ángel ; Martín, Miguel A.; Campos, Yolanda; Arenas, Joaquín; Garesse, Rafael artículo
openAccessOPA1 mutations.pdf.jpg2008OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypesAmati-Bonneau, Patrizia; Gallardo, M. Esther ; Bornstein, Belén ; Campos, Yolanda; Rivera, Henry; Martín, Miguel A.; Arenas, Joaquín; Garesse, Rafael ; Carelli, Valerioartículo
closedAccessaccesoRestringido.pdf.jpg2002The A8296G mtDNA mutation associated with several mitochondrial diseases does not cause mitochondrial dysfunction in cybrid cell linesBornstein, Belén ; Mas, José A.; Fernández-Moreno, Miguel Ángel ; Campos, Yolanda; Martín, Miguel A.; Arenas, Joaquín; Garesse, Rafael artículo
closedAccessaccesoRestringido.pdf.jpg2000The pathogenic role of point mutations affecting the translational initiation codon of mitochondrial genesFernández-Moreno, Miguel Ángel ; Bornstein, Belén ; Campos, Yolanda; Arenas, Joaquín; Garesse, Rafael artículo