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Diseases of the human mitochondrial oxidative phosphorylation system.
Montoya J, López-Gallardo E, Herrero-Martín MD, Martínez-Romero I, Gómez-Durán A, Pacheu D, Carreras M, Díez-Sánchez C, López-Pérez MJ, Ruiz-Pesini E. Montoya J, et al. Among authors: martinez romero i. Adv Exp Med Biol. 2009;652:47-67. doi: 10.1007/978-90-481-2813-6_5. Adv Exp Med Biol. 2009. PMID: 20225019 Review.
New MT-ND1 pathologic mutation for Leber hereditary optic neuropathy.
Martínez-Romero Í, Herrero-Martín MD, Llobet L, Emperador S, Martín-Navarro A, Narberhaus B, Ascaso FJ, López-Gallardo E, Montoya J, Ruiz-Pesini E. Martínez-Romero Í, et al. Clin Exp Ophthalmol. 2014 Dec;42(9):856-64. doi: 10.1111/ceo.12355. Epub 2014 May 30. Clin Exp Ophthalmol. 2014. PMID: 24800637
Oxidative phosphorylation differences between mitochondrial DNA haplogroups modify the risk of Leber's hereditary optic neuropathy.
Gómez-Durán A, Pacheu-Grau D, Martínez-Romero I, López-Gallardo E, López-Pérez MJ, Montoya J, Ruiz-Pesini E. Gómez-Durán A, et al. Among authors: martinez romero i. Biochim Biophys Acta. 2012 Aug;1822(8):1216-22. doi: 10.1016/j.bbadis.2012.04.014. Epub 2012 Apr 26. Biochim Biophys Acta. 2012. PMID: 22561905 Free article.