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.
83 related articles for article (PubMed ID: 1297821)
21. Multiple carboxylase deficiency: inherited and acquired disorders of biotin metabolism. Baumgartner ER; Suormala T Int J Vitam Nutr Res; 1997; 67(5):377-84. PubMed ID: 9350481 [TBL] [Abstract][Full Text] [Related]
22. Molecular analysis of new Japanese patients with holocarboxylase synthetase deficiency. Sakamoto O; Suzuki Y; Aoki Y; Li X; Hiratsuka M; Yanagihara K; Inui K; Okabe T; Yamaguchi S; Kudoh J; Shimizu N; Narisawa K J Inherit Metab Dis; 1998 Dec; 21(8):873-4. PubMed ID: 9870216 [No Abstract] [Full Text] [Related]
23. [Biotinidase deficiency. Its form of presentation and response to treatment]. Campistol J; Vilaseca MA; Ribes A; Riudor E An Esp Pediatr; 1996 Apr; 44(4):389-92. PubMed ID: 8796946 [No Abstract] [Full Text] [Related]
24. [Biotin-responsive multiple carboxylase deficiency]. Yoshida I Ryoikibetsu Shokogun Shirizu; 2000; (32):353-7. PubMed ID: 11212743 [No Abstract] [Full Text] [Related]
25. Lactic acidosis in biotin-responsive multiple carboxylase deficiency caused by holocarboxylase synthetase deficiency of early and late onset. Sherwood WG; Saunders M; Robinson BH; Brewster T; Gravel RA J Pediatr; 1982 Oct; 101(4):546-50. PubMed ID: 6811711 [TBL] [Abstract][Full Text] [Related]
26. Rapid differential diagnosis of carboxylase deficiencies and evaluation for biotin-responsiveness in a single blood sample. Suormala T; Wick H; Bonjour JP; Baumgartner ER Clin Chim Acta; 1985 Jan; 145(2):151-62. PubMed ID: 3918814 [TBL] [Abstract][Full Text] [Related]
28. A new case of holocarboxylase synthetase deficiency. Briones P; Ribes A; Vilaseca MA; RodrĂguez-Valcárcel G; Thuy LP; Sweetman L J Inherit Metab Dis; 1989; 12(3):329-30. PubMed ID: 2515377 [No Abstract] [Full Text] [Related]
29. Lipid metabolism in biotin-responsive multiple carboxylase deficiency. Gonzalez-Rios MC; Whitney SC; Williams ML; Elias PM; Packman S J Inherit Metab Dis; 1985; 8(4):184-6. PubMed ID: 2878112 [No Abstract] [Full Text] [Related]
30. Holocarboxylase synthetase deficiency: early diagnosis and management of a new case. Fuchshuber A; Suormala T; Roth B; Duran M; Michalk D; Baumgartner ER Eur J Pediatr; 1993 May; 152(5):446-9. PubMed ID: 8319716 [TBL] [Abstract][Full Text] [Related]
31. Prenatal diagnosis of holocarboxylase synthetase deficiency by assay of the enzyme in chorionic villus material followed by prenatal treatment. Thuy LP; Jurecki E; Nemzer L; Nyhan WL Clin Chim Acta; 1999 Jun; 284(1):59-68. PubMed ID: 10437643 [TBL] [Abstract][Full Text] [Related]