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23. Simon has biotinidase deficiency. Monsma M; Chibak M; Eleniak D AARN News Lett; 1988 Nov; 44(10):4-5. PubMed ID: 3195302 [No Abstract] [Full Text] [Related]
24. Biotin-responsive multiple carboxylase deficiency in an 8-year-old boy with normal serum biotinidase and fibroblast holocarboxylase-synthetase activities. Holme E; Jacobson CE; Kristiansson B J Inherit Metab Dis; 1988; 11(3):270-6. PubMed ID: 3148068 [TBL] [Abstract][Full Text] [Related]
25. Rat as a potential model for hearing loss in biotinidase deficiency. Rybak LP; Whitworth C; Scott V; Weberg AD; Bhardwaj B Ann Otol Rhinol Laryngol; 1991 Apr; 100(4 Pt 1):294-300. PubMed ID: 2018287 [TBL] [Abstract][Full Text] [Related]
26. The clinical spectrum of biotin-treatable encephalopathies in Saudi Arabia. Dabbagh O; Brismar J; Gascon GG; Ozand PT Brain Dev; 1994 Nov; 16 Suppl():72-80. PubMed ID: 7726384 [TBL] [Abstract][Full Text] [Related]
27. Human biotinidase isn't just for recycling biotin. Hymes J; Wolf B J Nutr; 1999 Feb; 129(2S Suppl):485S-489S. PubMed ID: 10064314 [TBL] [Abstract][Full Text] [Related]
29. Biotinidase and its roles in biotin metabolism. Hymes J; Wolf B Clin Chim Acta; 1996 Nov; 255(1):1-11. PubMed ID: 8930409 [TBL] [Abstract][Full Text] [Related]
31. Localization of biotinidase in the brain: implications for its role in hearing loss in biotinidase deficiency. Heller AJ; Stanley C; Shaia WT; Sismanis A; Spencer RF; Wolf B Hear Res; 2002 Nov; 173(1-2):62-8. PubMed ID: 12372635 [TBL] [Abstract][Full Text] [Related]
35. Biotinidase deficiency: the enzymatic defect in late-onset multiple carboxylase deficiency. Wolf B; Grier RE; Allen RJ; Goodman SI; Kien CL Clin Chim Acta; 1983 Jul; 131(3):273-81. PubMed ID: 6883721 [TBL] [Abstract][Full Text] [Related]
36. Intestinal absorption and renal excretion of biotin in patients with biotinidase deficiency. Suormala T; Wick H; Bonjour JP; Baumgartner ER Eur J Pediatr; 1985 May; 144(1):21-6. PubMed ID: 3926500 [TBL] [Abstract][Full Text] [Related]
37. Biotinidase deficiency--a treatable entity. Gulati S; Passi GR; Kumar A; Kabra M; Kalra V; Verma IC Indian J Pediatr; 2000 Jun; 67(6):464-6. PubMed ID: 10932969 [TBL] [Abstract][Full Text] [Related]
38. Prenatal diagnosis of heterozygosity for biotinidase deficiency by enzymatic and molecular analyses. Pomponio RJ; Hymes J; Pandya A; Landa B; Melone P; Javaheri R; Mardach R; Morton SW; Meyers GA; Reynolds T; Buck G; Nance WE; Wolf B Prenat Diagn; 1998 Feb; 18(2):117-22. PubMed ID: 9516011 [TBL] [Abstract][Full Text] [Related]
39. Biotinidase deficiency: the possible role of biotinidase in the processing of dietary protein-bound biotin. Wolf B; Heard GS; McVoy JR; Raetz HM J Inherit Metab Dis; 1984; 7 Suppl 2():121-2. PubMed ID: 6434861 [No Abstract] [Full Text] [Related]
40. Enzyme studies in combined carboxylase deficiency. Bartlett K; Ghneim HK; Stirk JH; Wastell HJ; Sherratt HS; Leonard JV Ann N Y Acad Sci; 1985; 447():235-51. PubMed ID: 2861780 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]