318 related articles for article (PubMed ID: 6811711)
21. A combined defect of three mitochondrial carboxylases presenting as biotin-responsive 3-methylcrotonyl glycinuria and 3-hydroxyisovaleric aciduria.
Bartlett K; Ng H; Leonard JV
Clin Chim Acta; 1980 Jan; 100(2):183-6. PubMed ID: 6766095
[TBL] [Abstract][Full Text] [Related]
22. Biotin in clinical medicine--a review.
Roth KS
Am J Clin Nutr; 1981 Sep; 34(9):1967-74. PubMed ID: 6116428
[TBL] [Abstract][Full Text] [Related]
23. Clinical and biochemical findings on a child with multiple biotin-responsive carboxylase deficiencies.
Narisawa K; Arai N; Igarashi Y; Satoh T; Tada K; Hirooka Y
J Inherit Metab Dis; 1982; 5(2):67-8. PubMed ID: 6133032
[No Abstract] [Full Text] [Related]
24. Multiple carboxylase deficiency.
Nyhan WL
Int J Biochem; 1988; 20(4):363-70. PubMed ID: 3284772
[TBL] [Abstract][Full Text] [Related]
25. Late-onset holocarboxylase synthetase deficiency.
Gibson KM; Bennett MJ; Nyhan WL; Mize CE
J Inherit Metab Dis; 1996; 19(6):739-42. PubMed ID: 8982946
[TBL] [Abstract][Full Text] [Related]
26. Deficiency of propionyl-Co A carboxylase and methylcrotonyl-Co A carboxylase in a patient with methylcrotonylglycinuria.
Weyler W; Sweetman L; Maggio DC; Nyhan WL
Clin Chim Acta; 1977 May; 76(3):321-8. PubMed ID: 858206
[TBL] [Abstract][Full Text] [Related]
27. Biotin holocarboxylase synthetase deficiency.
Sweetman L; Burri BJ; Nyhan WL
Ann N Y Acad Sci; 1985; 447():288-96. PubMed ID: 3860175
[No Abstract] [Full Text] [Related]
28. Fatty-acid-responsive alopecia in multiple carboxylase deficiency.
Munnich A; Saudubray JM; Coude FX; Charpentier C; Saurat JH; Frezal J
Lancet; 1980 May; 1(8177):1080-1. PubMed ID: 6103410
[No Abstract] [Full Text] [Related]
29. Prenatal administration of biotin in biotin responsive multiple carboxylase deficiency.
Roth KS; Yang W; Allan L; Saunders M; Gravel RA; Dakshinamurti K
Pediatr Res; 1982 Feb; 16(2):126-9. PubMed ID: 6799930
[TBL] [Abstract][Full Text] [Related]
30. The measurement of propionyl-CoA carboxylase and pyruvate carboxylase activity in hair roots: its use in the diagnosis of inherited biotin-dependent enzyme deficiencies.
Wolf B; Raetz H
Clin Chim Acta; 1983 May; 130(1):25-30. PubMed ID: 6851181
[TBL] [Abstract][Full Text] [Related]
31. Prenatal diagnosis and treatment of holocarboxylase synthetase deficiency.
Thuy LP; Belmont J; Nyhan WL
Prenat Diagn; 1999 Feb; 19(2):108-12. PubMed ID: 10215065
[TBL] [Abstract][Full Text] [Related]
32. [3H]biotin-labeled proteins in cultured human skin fibroblasts from patients with pyruvate carboxylase deficiency.
Robinson BH; Oei J; Saunders M; Gravel R
J Biol Chem; 1983 May; 258(10):6660-4. PubMed ID: 6406485
[TBL] [Abstract][Full Text] [Related]
33. Primary cultures of astrocytes from rat as a model for biotin deficiency in nervous tissue.
RodrÃguez-Pombo P; Sweetman L; Ugarte M
Mol Chem Neuropathol; 1992; 16(1-2):33-44. PubMed ID: 1520405
[TBL] [Abstract][Full Text] [Related]
34. Prenatal treatment of multiple carboxylase deficiency.
Roth KS
Ann N Y Acad Sci; 1985; 447():263-71. PubMed ID: 3925857
[No Abstract] [Full Text] [Related]
35. Prenatal treatment of biotin responsive multiple carboxylase deficiency.
Packman S; Cowan MJ; Golbus MS; Caswell NM; Sweetman L; Burri BJ; Nyhan WL; Baker H
Lancet; 1982 Jun; 1(8287):1435-8. PubMed ID: 6123722
[No Abstract] [Full Text] [Related]
36. Holocarboxylase synthetase deficiency: report of a case with onset in late infancy.
Touma E; Suormala T; Baumgartner ER; Gerbaka B; Ogier de Baulny H; Loiselet J
J Inherit Metab Dis; 1999 Apr; 22(2):115-22. PubMed ID: 10234606
[TBL] [Abstract][Full Text] [Related]
37. A bioassay for determining biotinidase activity and for discriminating biocytin from biotin using holocarboxylase synthetase-deficient cultured fibroblasts.
Weiner DL; Grier RE; Wolf B
J Inherit Metab Dis; 1985; 8 Suppl 2():101-2. PubMed ID: 3930849
[No Abstract] [Full Text] [Related]
38. Biotin uptake into human peripheral blood mononuclear cells increases early in the cell cycle, increasing carboxylase activities.
Stanley JS; Mock DM; Griffin JB; Zempleni J
J Nutr; 2002 Jul; 132(7):1854-9. PubMed ID: 12097659
[TBL] [Abstract][Full Text] [Related]
39. Biotin dependency due to a defect in biotin transport.
Mardach R; Zempleni J; Wolf B; Cannon MJ; Jennings ML; Cress S; Boylan J; Roth S; Cederbaum S; Mock DM
J Clin Invest; 2002 Jun; 109(12):1617-23. PubMed ID: 12070309
[TBL] [Abstract][Full Text] [Related]
40. Impaired intestinal absorption of biotin in juvenile multiple carboxylase deficiency.
Thoene JG; Lemons R; Baker H
N Engl J Med; 1983 Mar; 308(11):639-42. PubMed ID: 6828095
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]