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A novel RRM2B gene variant associated with Telbivudine-induced mitochondrial myopathy.
Hernández-Laín A, Guerrero AM, Domínguez-González C, Fernández-Vázquez I, Maya DG, Delmiro A, Arenas J, Morales JR, Blázquez A, Moran M, Martín MA. Hernández-Laín A, et al. Among authors: moran m. J Neurol Sci. 2015 Nov 15;358(1-2):481-3. doi: 10.1016/j.jns.2015.08.1550. Epub 2015 Sep 2. J Neurol Sci. 2015. PMID: 26359855 No abstract available.
Can patients with McArdle's disease run?
Pérez M, Moran M, Cardona C, Maté-Muñoz JL, Rubio JC, Andreu AL, Martin MA, Arenas J, Lucia A. Pérez M, et al. Among authors: moran m. Br J Sports Med. 2007 Jan;41(1):53-4. doi: 10.1136/bjsm.2006.030791. Epub 2006 Sep 25. Br J Sports Med. 2007. PMID: 17000713 Free PMC article.
Favorable responses to acute and chronic exercise in McArdle patients.
Maté-Muñoz JL, Moran M, Pérez M, Chamorro-Viña C, Gómez-Gallego F, Santiago C, Chicharro L, Foster C, Nogales-Gadea G, Rubio JC, Andreu AL, Martín MA, Arenas J, Lucia A. Maté-Muñoz JL, et al. Among authors: moran m. Clin J Sport Med. 2007 Jul;17(4):297-303. doi: 10.1097/JSM.0b013e3180f6168c. Clin J Sport Med. 2007. PMID: 17620784
Mitochondrial disorders due to nuclear OXPHOS gene defects.
Ugalde C, Morán M, Blázquez A, Arenas J, Martín MA. Ugalde C, et al. Among authors: moran m. Adv Exp Med Biol. 2009;652:85-116. doi: 10.1007/978-90-481-2813-6_7. Adv Exp Med Biol. 2009. PMID: 20225021 Review.
Marked mitochondrial DNA depletion associated with a novel SUCLG1 gene mutation resulting in lethal neonatal acidosis, multi-organ failure, and interrupted aortic arch.
Rivera H, Merinero B, Martinez-Pardo M, Arroyo I, Ruiz-Sala P, Bornstein B, Serra-Suhe C, Gallardo E, Marti R, Moran MJ, Ugalde C, Perez-Jurado LA, Andreu AL, Garesse R, Ugarte M, Arenas J, Martin MA. Rivera H, et al. Among authors: moran mj. Mitochondrion. 2010 Jun;10(4):362-8. doi: 10.1016/j.mito.2010.03.003. Epub 2010 Mar 19. Mitochondrion. 2010. PMID: 20227526
1,903 results