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Browsing by Author Rivera, Henry

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Issue DateTitleAuthor(s)Type
3-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, RafaelArtículo
2010Depleción del ácido desoxirribonucleico mitocondrial y mutaciones de POLG en un paciente con neuropatía sensorial atáxica, disartria y oftalmoplejíaPosada, Ignacio J.; Gallardo, M. Esther; Domínguez, Cristina; Rivera, Henry; Arenas, Joaquín; Martín, Miguel A.; Garesse, Rafael; Bornstein, BelénArtículo
2010Marked mitochondrial DNA depletion associated with a novel SUCLG1 gene mutation resulting in lethal neonatal acidosis, multi-organ failure, and interrupted aortic archRivera, Henry; Merinero, Begoña; Ruiz-Sala, Pedro; Bornstein, Belén; Gallardo, M. Esther; Garesse, Rafael; Ugarte, Magdalena; Martín, Miguel A.Artículo
2007Mild 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
2008OPA1 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

Showing results 1 to 5 of 5