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10. 3-Hydroxyisovalerylcarnitine in patients with deficiency of 3-methylcrotonyl CoA carboxylase. Röschinger W; Millington DS; Gage DA; Huang ZH; Iwamoto T; Yano S; Packman S; Johnston K; Berry SA; Sweetman L Clin Chim Acta; 1995 Aug; 240(1):35-51. PubMed ID: 8582058 [No Abstract] [Full Text] [Related]
11. Reassessment of biotin-responsiveness in "unresponsive" propionyl CoA carboxylase deficiency. Wolf B J Pediatr; 1980 Dec; 97(6):964-6. PubMed ID: 7441430 [No Abstract] [Full Text] [Related]
13. Biotin-reversible neurodegenerative disease in infancy. Low LC; Stephenson JB; Bartlett K; Seakins JW; Shaikh SA Aust Paediatr J; 1986 Feb; 22(1):65-8. PubMed ID: 3087340 [TBL] [Abstract][Full Text] [Related]
14. Two forms of biotin-responsive multiple carboxylase deficiency. Sweetman L J Inherit Metab Dis; 1981; 4(2):53-4. PubMed ID: 6790844 [TBL] [Abstract][Full Text] [Related]
15. Biotin-responsive in vivo carboxylase deficiency in two siblings with secretory diarrhea receiving total parenteral nutrition. Kien CL; Kohler E; Goodman SI; Berlow S; Hong R; Horowitz SP; Baker H J Pediatr; 1981 Oct; 99(4):546-50. PubMed ID: 6792336 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. Inherited disorders of 3-methylcrotonyl CoA carboxylation. Leonard JV; Seakins JW; Bartlett K; Hyde J; Wilson J; Clayton B Arch Dis Child; 1981 Jan; 56(1):53-9. PubMed ID: 7469453 [TBL] [Abstract][Full Text] [Related]