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.
132 related articles for article (PubMed ID: 37091464)
1. A Novel Mutation in the OXCT1 Gene Causing Succinyl-CoA:3-Ketoacid CoA Transferase (SCOT) Deficiency Starting with Neurologic Manifestations. Amirkashani D; Asadollahi M; Hosseini R; Talebi S; Golchehre Z; Keramatipour M Iran J Child Neurol; 2023; 17(2):127-133. PubMed ID: 37091464 [TBL] [Abstract][Full Text] [Related]
2. A case of severe acidosis in a 12-month-old: Succinyl-CoA:3-ketoacid Dhammi N; Essakow J; Gallagher R; Gaw C SAGE Open Med Case Rep; 2022; 10():2050313X221111274. PubMed ID: 35847427 [TBL] [Abstract][Full Text] [Related]
3. A Rare Cause of Life-Threatening Ketoacidosis: Novel Compound Heterozygous Kim YA; Kim SH; Cheon CK; Kim YM Yonsei Med J; 2019 Mar; 60(3):308-311. PubMed ID: 30799594 [TBL] [Abstract][Full Text] [Related]
4. A neonatal-onset succinyl-CoA:3-ketoacid CoA transferase (SCOT)-deficient patient with T435N and c.658-666dupAACGTGATT p.N220_I222dup mutations in the OXCT1 gene. Fukao T; Ishii T; Amano N; Kursula P; Takayanagi M; Murase K; Sakaguchi N; Kondo N; Hasegawa T J Inherit Metab Dis; 2010 Dec; 33 Suppl 3():S307-13. PubMed ID: 20652411 [TBL] [Abstract][Full Text] [Related]
5. A Case of Succinyl-CoA:3-Oxoacid CoA Transferase Deficiency Presenting with Severe Acidosis in a 14-Month-Old Female: Evidence for Pathogenicity of a Point Mutation in the Zheng DJ; Hooper M; Spencer-Manzon M; Pierce RW J Pediatr Intensive Care; 2018 Mar; 7(1):62-66. PubMed ID: 31073471 [TBL] [Abstract][Full Text] [Related]
6. When one disease is not enough: succinyl-CoA: 3-oxoacid coenzyme A transferase (SCOT) deficiency due to a novel mutation in OXCT1 in an infant with known phenylketonuria. Schwade JN; Endmann M; Hofmann T; Rust S; Sass JO; Rutsch F J Pediatr Endocrinol Metab; 2017 Oct; 30(10):1121-1124. PubMed ID: 28820737 [TBL] [Abstract][Full Text] [Related]
7. Heterozygous carriers of succinyl-CoA:3-oxoacid CoA transferase deficiency can develop severe ketoacidosis. Sasai H; Aoyama Y; Otsuka H; Abdelkreem E; Naiki Y; Kubota M; Sekine Y; Itoh M; Nakama M; Ohnishi H; Fujiki R; Ohara O; Fukao T J Inherit Metab Dis; 2017 Nov; 40(6):845-852. PubMed ID: 28695376 [TBL] [Abstract][Full Text] [Related]
8. Clinical variability and outcome of succinyl-CoA:3-ketoacid CoA transferase deficiency caused by a single OXCT1 mutation: Report of 17 cases. Alghamdi MA; Tohary M; Alzaidan H; Imtiaz F; Al-Hassnan ZN JIMD Rep; 2021 Nov; 62(1):91-96. PubMed ID: 34765403 [TBL] [Abstract][Full Text] [Related]
12. Clinical and molecular characterization of five patients with succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency. Fukao T; Sass JO; Kursula P; Thimm E; Wendel U; Ficicioglu C; Monastiri K; Guffon N; Barić I; Zabot MT; Kondo N Biochim Biophys Acta; 2011 May; 1812(5):619-24. PubMed ID: 21296660 [TBL] [Abstract][Full Text] [Related]
13. Inborn errors of ketone body utilization. Hori T; Yamaguchi S; Shinkaku H; Horikawa R; Shigematsu Y; Takayanagi M; Fukao T Pediatr Int; 2015; 57(1):41-8. PubMed ID: 25559898 [TBL] [Abstract][Full Text] [Related]
14. Single-base substitution at the last nucleotide of exon 6 (c.671G>A), resulting in the skipping of exon 6, and exons 6 and 7 in human succinyl-CoA:3-ketoacid CoA transferase (SCOT) gene. Yamada K; Fukao T; Zhang G; Sakurai S; Ruiter JP; Wanders RJ; Kondo N Mol Genet Metab; 2007 Mar; 90(3):291-7. PubMed ID: 17169596 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. Patients homozygous for the T435N mutation of succinyl-CoA:3-ketoacid CoA Transferase (SCOT) do not show permanent ketosis. Fukao T; Shintaku H; Kusubae R; Zhang GX; Nakamura K; Kondo M; Kondo N Pediatr Res; 2004 Dec; 56(6):858-63. PubMed ID: 15496607 [TBL] [Abstract][Full Text] [Related]
17. Successful adaptation to ketosis by mice with tissue-specific deficiency of ketone body oxidation. Cotter DG; Schugar RC; Wentz AE; d'Avignon DA; Crawford PA Am J Physiol Endocrinol Metab; 2013 Feb; 304(4):E363-74. PubMed ID: 23233542 [TBL] [Abstract][Full Text] [Related]
18. Identification and characterization of a temperature-sensitive R268H mutation in the human succinyl-CoA:3-ketoacid CoA transferase (SCOT) gene. Fukao T; Kursula P; Owen EP; Kondo N Mol Genet Metab; 2007 Nov; 92(3):216-21. PubMed ID: 17706444 [TBL] [Abstract][Full Text] [Related]
19. Impact of peripheral ketolytic deficiency on hepatic ketogenesis and gluconeogenesis during the transition to birth. Cotter DG; Ercal B; d'Avignon DA; Dietzen DJ; Crawford PA J Biol Chem; 2013 Jul; 288(27):19739-49. PubMed ID: 23689508 [TBL] [Abstract][Full Text] [Related]
20. Successful Management of Pregnancies in Patients with Inherited Disorders of Ketone Body Metabolism. Sulaiman RA; Al-Nemer M; Khan R; Almasned M; Handoum BS; Al-Hassnan ZN JIMD Rep; 2018; 38():41-44. PubMed ID: 28488182 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]