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11. A new Japanese case of succinyl-CoA: 3-ketoacid CoA-transferase deficiency. Sakazaki H; Hirayama K; Murakami S; Yonezawa S; Shintaku H; Sawada Y; Fukao T; Watanabe H; Orii T; Isshiki G J Inherit Metab Dis; 1995; 18(3):323-5. PubMed ID: 7474899 [No Abstract] [Full Text] [Related]
12. Management and communication problems in a patient with succinyl-CoA transferase deficiency in pregnancy and labour. Merron S; Akhtar R Int J Obstet Anesth; 2009 Jul; 18(3):280-3. PubMed ID: 19450972 [TBL] [Abstract][Full Text] [Related]
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14. Disorders of ketone production and utilization. Kayer MA Mol Genet Metab; 2006 Apr; 87(4):281-3. PubMed ID: 16622911 [No Abstract] [Full Text] [Related]
15. Hyperketotic states due to inherited defects of ketolysis. Saudubray JM; Specola N; Middleton B; Lombes A; Bonnefont JP; Jakobs C; Vassault A; Charpentier C; Day R Enzyme; 1987; 38(1-4):80-90. PubMed ID: 2894307 [TBL] [Abstract][Full Text] [Related]
16. Succinyl-CoA:3-ketoacid transferase (SCOT) deficiency in a new patient homozygous for an R217X mutation. Longo N; Fukao T; Singh R; Pasquali M; Barrios RG; Kondo N; Gibson KM J Inherit Metab Dis; 2004; 27(5):691-2. PubMed ID: 15669687 [TBL] [Abstract][Full Text] [Related]
17. Succinyl-CoA:3-ketoacid coenzyme A transferase (SCOT): development of an antibody to human SCOT and diagnostic use in hereditary SCOT deficiency. Song XQ; Fukao T; Mitchell GA; Kassovska-Bratinova S; Ugarte M; Wanders RJ; Hirayama K; Shintaku H; Churchill P; Watanabe H; Orii T; Kondo N Biochim Biophys Acta; 1997 Apr; 1360(2):151-6. PubMed ID: 9128180 [TBL] [Abstract][Full Text] [Related]
19. Early prenatal diagnosis in two pregnancies at risk for glutaryl-CoA dehydrogenase deficiency. Holme E; Kyllerman M; Lindstedt S J Inherit Metab Dis; 1989; 12 Suppl 2():280-2. PubMed ID: 2512426 [No Abstract] [Full Text] [Related]
20. The prenatal diagnosis of inborn errors of metabolism. Milunsky A; Littlefield JW Annu Rev Med; 1972; 23():57-76. PubMed ID: 4264784 [No Abstract] [Full Text] [Related] [Next] [New Search]