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.
5. 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]
6. Gender-specific occurrence of West syndrome in patients with pyruvate dehydrogenase complex deficiency. Naito E; Ito M; Yokota I; Saijo T; Ogawa Y; Shinahara K; Kuroda Y Neuropediatrics; 2001 Dec; 32(6):295-8. PubMed ID: 11870584 [TBL] [Abstract][Full Text] [Related]
7. Molecular analysis of abnormal pyruvate dehydrogenase in a patient with thiamine-responsive congenital lactic acidemia. Naito E; Ito M; Takeda E; Yokota I; Yoshijima S; Kuroda Y Pediatr Res; 1994 Sep; 36(3):340-6. PubMed ID: 7808831 [TBL] [Abstract][Full Text] [Related]
8. A family with pyruvate dehydrogenase complex deficiency due to a novel C>T substitution at nucleotide position 407 in exon 4 of the X-linked Epsilon1alpha gene. Tulinius M; Darin N; Wiklund LM; Holmberg E; Eriksson JE; Lissens W; De Meirleir L; Holme E Eur J Pediatr; 2005 Feb; 164(2):99-103. PubMed ID: 15558317 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. Neurodevelopmental abnormalities and lactic acidosis in a girl with a 20-bp deletion in the X-linked pyruvate dehydrogenase E1 alpha subunit gene. Matthews PM; Brown RM; Otero L; Marchington D; Leonard JV; Brown GK Neurology; 1993 Oct; 43(10):2025-30. PubMed ID: 7692352 [TBL] [Abstract][Full Text] [Related]
12. Diagnosis and molecular analysis of three male patients with thiamine-responsive pyruvate dehydrogenase complex deficiency. Naito E; Ito M; Yokota I; Saijo T; Ogawa Y; Kuroda Y J Neurol Sci; 2002 Sep; 201(1-2):33-7. PubMed ID: 12163191 [TBL] [Abstract][Full Text] [Related]
13. Spectrum of neurological and survival outcomes in pyruvate dehydrogenase complex (PDC) deficiency: lack of correlation with genotype. DeBrosse SD; Okajima K; Zhang S; Nakouzi G; Schmotzer CL; Lusk-Kopp M; Frohnapfel MB; Grahame G; Kerr DS Mol Genet Metab; 2012 Nov; 107(3):394-402. PubMed ID: 23021068 [TBL] [Abstract][Full Text] [Related]
14. Ornithine transcarbamylase deficiency in females: an often overlooked cause of treatable encephalopathy. Pridmore CL; Clarke JT; Blaser S J Child Neurol; 1995 Sep; 10(5):369-74. PubMed ID: 7499756 [TBL] [Abstract][Full Text] [Related]