Kiilerich K, Birk JB, Damsgaard R, Wojtaszewski JF, Pilegaard H (Jan 2008). "Regulation of PDH in human arm and leg muscles at rest and during intense exercise". American Journal of Physiology. Endocrinology and Metabolism. 294 (1): E36–42. doi:10.1152/ajpendo.00352.2007. PMID17957032.
Imbard A, Boutron A, Vequaud C, Zater M, de Lonlay P, de Baulny HO, Barnerias C, Miné M, Marsac C, Saudubray JM, Brivet M (Dec 2011). "Molecular characterization of 82 patients with pyruvate dehydrogenase complex deficiency. Structural implications of novel amino acid substitutions in E1 protein". Molecular Genetics and Metabolism. 104 (4): 507–16. doi:10.1016/j.ymgme.2011.08.008. PMID21914562.
Sharma R, Sharrard MJ, Connolly DJ, Mordekar SR (May 2012). "Unilateral periventricular leukomalacia in association with pyruvate dehydrogenase deficiency". Developmental Medicine and Child Neurology. 54 (5): 469–71. doi:10.1111/j.1469-8749.2011.04108.x. PMID21895644. S2CID10729481.
Willemsen M, Rodenburg RJ, Teszas A, van den Heuvel L, Kosztolanyi G, Morava E (Jun 2006). "Females with PDHA1 gene mutations: a diagnostic challenge". Mitochondrion. 6 (3): 155–9. doi:10.1016/j.mito.2006.03.001. PMID16713755.
Kiilerich K, Birk JB, Damsgaard R, Wojtaszewski JF, Pilegaard H (Jan 2008). "Regulation of PDH in human arm and leg muscles at rest and during intense exercise". American Journal of Physiology. Endocrinology and Metabolism. 294 (1): E36–42. doi:10.1152/ajpendo.00352.2007. PMID17957032.
Magner M, Vinšová K, Tesařová M, Hájková Z, Hansíková H, Wenchich L, Ješina P, Smolka V, Adam T, Vaněčková M, Zeman J, Honzík T (2011). "Two patients with clinically distinct manifestation of pyruvate dehydrogenase deficiency due to mutations in PDHA1 gene". Prague Medical Report. 112 (1): 18–28. PMID21470495.
Imbard A, Boutron A, Vequaud C, Zater M, de Lonlay P, de Baulny HO, Barnerias C, Miné M, Marsac C, Saudubray JM, Brivet M (Dec 2011). "Molecular characterization of 82 patients with pyruvate dehydrogenase complex deficiency. Structural implications of novel amino acid substitutions in E1 protein". Molecular Genetics and Metabolism. 104 (4): 507–16. doi:10.1016/j.ymgme.2011.08.008. PMID21914562.
Sharma R, Sharrard MJ, Connolly DJ, Mordekar SR (May 2012). "Unilateral periventricular leukomalacia in association with pyruvate dehydrogenase deficiency". Developmental Medicine and Child Neurology. 54 (5): 469–71. doi:10.1111/j.1469-8749.2011.04108.x. PMID21895644. S2CID10729481.
Willemsen M, Rodenburg RJ, Teszas A, van den Heuvel L, Kosztolanyi G, Morava E (Jun 2006). "Females with PDHA1 gene mutations: a diagnostic challenge". Mitochondrion. 6 (3): 155–9. doi:10.1016/j.mito.2006.03.001. PMID16713755.
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"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
Sharma R, Sharrard MJ, Connolly DJ, Mordekar SR (May 2012). "Unilateral periventricular leukomalacia in association with pyruvate dehydrogenase deficiency". Developmental Medicine and Child Neurology. 54 (5): 469–71. doi:10.1111/j.1469-8749.2011.04108.x. PMID21895644. S2CID10729481.