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5. Inborn errors of biotin metabolism. Clinical and laboratory features of eight cases. Coşkun T; Tokatli A; Ozalp I Turk J Pediatr; 1994; 36(4):267-78. PubMed ID: 7825232 [TBL] [Abstract][Full Text] [Related]
6. Biotin-responsive multiple carboxylase deficiency and immunodeficiency. Williams ML Curr Probl Dermatol; 1989; 18():89-92. PubMed ID: 2663376 [No Abstract] [Full Text] [Related]
7. 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]
8. 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]
9. [Importance of biotin metabolism]. Rodríguez Meléndez R Rev Invest Clin; 2000; 52(2):194-9. PubMed ID: 10846444 [TBL] [Abstract][Full Text] [Related]
10. [Biotinidase deficiency: importance of its neonatal diagnosis and early treatment]. Couce Pico ML; Martinón-Torres F; Castiñeiras DE; Alonso-Fernández JR; Fraga JM An Esp Pediatr; 1999 May; 50(5):504-6. PubMed ID: 10394193 [No Abstract] [Full Text] [Related]
11. Biotinidase deficiency in juvenile multiple carboxylase deficiency. Thoene J; Wolf B Lancet; 1983 Aug; 2(8346):398. PubMed ID: 6135890 [No Abstract] [Full Text] [Related]
18. Biotinidase deficiency associated with renal loss of biocytin and biotin. Baumgartner ER; Suormala T; Wick H; Bausch J; Bonjour JP Ann N Y Acad Sci; 1985; 447():272-87. PubMed ID: 3925858 [TBL] [Abstract][Full Text] [Related]
20. A new solid-phase assay for biotin and biocytin and its application to the study of patients with biotinidase deficiency. Chan PW; Bartlett K Clin Chim Acta; 1986 Sep; 159(2):185-96. PubMed ID: 3095002 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]