These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
136 related articles for article (PubMed ID: 12917150)
1. In vivo pyruvate detected by MR spectroscopy in neonatal pyruvate dehydrogenase deficiency. Zand DJ; Simon EM; Pulitzer SB; Wang DJ; Wang ZJ; Rorke LB; Palmieri M; Berry GT AJNR Am J Neuroradiol; 2003 Aug; 24(7):1471-4. PubMed ID: 12917150 [TBL] [Abstract][Full Text] [Related]
2. Prenatal diagnosis of pyruvate dehydrogenase deficiency using magnetic resonance imaging. Robinson JN; Norwitz ER; Mulkern R; Brown SA; Rybicki F; Tempany CM Prenat Diagn; 2001 Dec; 21(12):1053-6. PubMed ID: 11746163 [TBL] [Abstract][Full Text] [Related]
3. Clinical diversity of pyruvate dehydrogenase deficiency. Cross JH; Connelly A; Gadian DG; Kendall BE; Brown GK; Brown RM; Leonard JV Pediatr Neurol; 1994 Jun; 10(4):276-83. PubMed ID: 8068153 [TBL] [Abstract][Full Text] [Related]
4. Unilateral periventricular leukomalacia in association with pyruvate dehydrogenase deficiency. Sharma R; Sharrard MJ; Connolly DJ; Mordekar SR Dev Med Child Neurol; 2012 May; 54(5):469-71. PubMed ID: 21895644 [TBL] [Abstract][Full Text] [Related]
5. Neonatal pyruvate dehydrogenase deficiency due to a R302H mutation in the PDHA1 gene: MRI findings. Soares-Fernandes JP; Teixeira-Gomes R; Cruz R; Ribeiro M; Magalhães Z; Rocha JF; Leijser LM Pediatr Radiol; 2008 May; 38(5):559-62. PubMed ID: 18197404 [TBL] [Abstract][Full Text] [Related]
8. Therapeutic efficacy of a case of pyruvate dehydrogenase complex deficiency monitored by localized proton magnetic resonance spectroscopy. Harada M; Tanouchi M; Arai K; Nishitani H; Miyoshi H; Hashimoto T Magn Reson Imaging; 1996; 14(1):129-33. PubMed ID: 8656986 [TBL] [Abstract][Full Text] [Related]
9. Defects of pyruvate metabolism and the Krebs cycle. De Meirleir L J Child Neurol; 2002 Dec; 17 Suppl 3():3S26-33; discussion 3S33-4. PubMed ID: 12597053 [TBL] [Abstract][Full Text] [Related]
11. Hyperpolarized [1-13C] pyruvate MR spectroscopy detect altered glycolysis in the brain of a cognitively impaired mouse model fed high-fat diet. Choi YS; Kang S; Ko SY; Lee S; Kim JY; Lee H; Song JE; Kim DH; Kim E; Kim CH; Saksida L; Song HT; Lee JE Mol Brain; 2018 Dec; 11(1):74. PubMed ID: 30563553 [TBL] [Abstract][Full Text] [Related]
12. DNA diagnosis of pyruvate dehydrogenase deficiency in female patients with congenital lactic acidaemia. Matsuda J; Ito M; Naito E; Yokota I; Kuroda Y J Inherit Metab Dis; 1995; 18(5):534-46. PubMed ID: 8598634 [TBL] [Abstract][Full Text] [Related]
13. Prenatal diagnosis of pyruvate dehydrogenase E1 alpha subunit deficiency. Brown RM; Brown GK Prenat Diagn; 1994 Jun; 14(6):435-41. PubMed ID: 7937579 [TBL] [Abstract][Full Text] [Related]
14. Selective galactose culture condition reveals distinct metabolic signatures in pyruvate dehydrogenase and complex I deficient human skin fibroblasts. Hertig D; Felser A; Diserens G; Kurth S; Vermathen P; Nuoffer JM Metabolomics; 2019 Feb; 15(3):32. PubMed ID: 30830487 [TBL] [Abstract][Full Text] [Related]