117 related articles for article (PubMed ID: 9521962)
1. Succinyl-CoA:3-ketoacid CoA-transferase deficiency.
Snyderman SE; Sansaricq C; Middleton B
Pediatrics; 1998 Apr; 101(4 Pt 1):709-11. PubMed ID: 9521962
[No Abstract] [Full Text] [Related]
2. [Succinyl-CoA: 3-ketoacid CoA transferase deficiency].
Yamaguchi S
Ryoikibetsu Shokogun Shirizu; 2001; (34 Pt 2):701-2. PubMed ID: 11528975
[No Abstract] [Full Text] [Related]
3. 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]
4. [Succinyl-CoA: 3-ketoacid CoA transferase deficiency].
Fukao T
Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):355-8. PubMed ID: 9590068
[No Abstract] [Full Text] [Related]
5. Prenatal diagnosis of succinyl-coenzyme A:3-ketoacid coenzyme A transferase deficiency.
Fukao T; Song XQ; Watanabe H; Hirayama K; Sakazaki H; Shintaku H; Imanaka M; Orii T; Kondo N
Prenat Diagn; 1996 May; 16(5):471-4. PubMed ID: 8844009
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Succinyl-CoA:acetoacetate transferase deficiency. Identification of a new case; prenatal exclusion in three further pregnancies.
Rolland MO; Guffon N; Mandon G; Divry P
J Inherit Metab Dis; 1998 Aug; 21(6):687-8. PubMed ID: 9762611
[No Abstract] [Full Text] [Related]
8. Two siblings with episodic ketoacidosis and decreased activity of succinyl-CoA:3-ketoacid CoA-transferase in cultured fibroblasts.
Pretorius CJ; Loy Son GG; Bonnici F; Harley EH
J Inherit Metab Dis; 1996; 19(3):296-300. PubMed ID: 8803771
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Effect of microgravity on metabolic enzymes of individual muscle fibers.
Manchester JK; Chi MM; Norris B; Ferrier B; Krasnov I; Nemeth PM; McDougal DB; Lowry OH
FASEB J; 1990 Jan; 4(1):55-63. PubMed ID: 1967237
[TBL] [Abstract][Full Text] [Related]
11. Ketone body metabolism and its defects.
Fukao T; Mitchell G; Sass JO; Hori T; Orii K; Aoyama Y
J Inherit Metab Dis; 2014 Jul; 37(4):541-51. PubMed ID: 24706027
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Succinyl-CoA:acetoacetate transferase deficiency: identification of a new patient with a neonatal onset and review of the literature.
Niezen-Koning KE; Wanders RJ; Ruiter JP; Ijlst L; Visser G; Reitsma-Bierens WC; Heymans HS; Reijngoud DJ; Smit GP
Eur J Pediatr; 1997 Nov; 156(11):870-3. PubMed ID: 9392403
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Characterization of an acyl-CoA: carboxylate CoA-transferase from Aspergillus nidulans involved in propionyl-CoA detoxification.
Fleck CB; Brock M
Mol Microbiol; 2008 May; 68(3):642-56. PubMed ID: 18331473
[TBL] [Abstract][Full Text] [Related]
16. [The correlation between activity of enzymes participating in the formation and utilization of acetyl CoA in rabbit heart mitochondria in myocarditis and normal state].
Sharkova EV
Vopr Med Khim; 1975; 21(6):625-9. PubMed ID: 3026
[TBL] [Abstract][Full Text] [Related]
17. Neonatal hypoglycaemia in severe succinyl-CoA: 3-oxoacid CoA-transferase deficiency.
Berry GT; Fukao T; Mitchell GA; Mazur A; Ciafre M; Gibson J; Kondo N; Palmieri MJ
J Inherit Metab Dis; 2001 Oct; 24(5):587-95. PubMed ID: 11757586
[TBL] [Abstract][Full Text] [Related]
18. A 6-bp deletion at the splice donor site of the first intron resulted in aberrant splicing using a cryptic splice site within exon 1 in a patient with succinyl-CoA: 3-Ketoacid CoA transferase (SCOT) deficiency.
Fukao T; Sakurai S; Rolland MO; Zabot MT; Schulze A; Yamada K; Kondo N
Mol Genet Metab; 2006 Nov; 89(3):280-2. PubMed ID: 16765626
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. A new case of succinyl-CoA: acetoacetate transferase deficiency.
Pérez-Cerdá C; Merinero B; Sanz P; Jiménez A; Hernández C; García MJ; Ugarte M
J Inherit Metab Dis; 1992; 15(3):371-3. PubMed ID: 1405472
[No Abstract] [Full Text] [Related]
[Next] [New Search]
