1. Sproule DM, Dyme J, Coku J, de Vinck D, Rosenzweig E, Chung WK, et al. Pulmonary artery hypertension in a child with MELAS due to a point mutation of the mitochondrial tRNA((Leu)) gene (m.3243A>G). J Inherit Metab Dis. 2008. (in press).
Article
2. Barclay AR, Sholler G, Christodolou J, Shun A, Arbuckle S, Dorney S, et al. Pulmonary hypertension -- a new manifestation of mitochondrial disease. J Inherit Metab Dis. 2005. 28:1081–1089.
Article
3. Van Hove JL, Freehauf C, Miyamoto S, Vladutiu GD, Pancrudo J, Bonilla E, et al. Infantile cardiomyopathy caused by the T14709C mutation in the mitochondrial tRNA glutamic acid gene. Eur J Pediatr. 2008. 167:771–776.
Article
4. Klein A, Fasnacht M, Huisman TA, Neuhaus TJ, Martin E, Boltshauser E. Siblings with infantile cerebral stroke and delayed multivessel involvement -- a new hereditary vasculopathy? Eur J Paediatr Neurol. 2007. 11:292–296.
Article
5. Venditti CP, Harris MC, Huff D, Peterside I, Munson D, Weber HS, et al. Congenital cardiomyopathy and pulmonary hypertension: another fatal variant of cytochrome-c oxidase deficiency. J Inherit Metab Dis. 2004. 27:735–739.
Article
6. Waypa GB, Schumacker PT. Role for mitochondrial reactive oxygen species in hypoxic pulmonary vasoconstriction. Novartis Found Symp. 2006. 272:176–192. discussion 192-5, 214-7.
Article