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23. Transcobalamin in cultured fibroblasts from patients with inborn errors of vitamin B12 metabolism. Yamani L; Gibbs BF; Gilfix BM; Watkins D; Hosack A; Rosenblatt DS Mol Genet Metab; 2008; 95(1-2):104-6. PubMed ID: 18606554 [TBL] [Abstract][Full Text] [Related]
24. Cobalamin and folate deficiency: acquired and hereditary disorders in children. Rosenblatt DS; Whitehead VM Semin Hematol; 1999 Jan; 36(1):19-34. PubMed ID: 9930566 [TBL] [Abstract][Full Text] [Related]
25. Defect in vitamin B12 release from lysosomes: newly described inborn error of vitamin B12 metabolism. Rosenblatt DS; Hosack A; Matiaszuk NV; Cooper BA; Laframboise R Science; 1985 Jun; 228(4705):1319-21. PubMed ID: 4001945 [TBL] [Abstract][Full Text] [Related]
26. Inherited disorders of cobalamin metabolism. Qureshi AA; Rosenblatt DS; Cooper BA Crit Rev Oncol Hematol; 1994 Oct; 17(2):133-51. PubMed ID: 7818787 [No Abstract] [Full Text] [Related]
27. Added value of next generation gene panel analysis for patients with elevated methylmalonic acid and no clinical diagnosis following functional studies of vitamin B12 metabolism. Pupavac M; Tian X; Chu J; Wang G; Feng Y; Chen S; Fenter R; Zhang VW; Wang J; Watkins D; Wong LJ; Rosenblatt DS Mol Genet Metab; 2016 Mar; 117(3):363-8. PubMed ID: 26827111 [TBL] [Abstract][Full Text] [Related]
28. Inherited errors of cobalamin metabolism and their management. Linnell JC; Bhatt HR Baillieres Clin Haematol; 1995 Sep; 8(3):567-601. PubMed ID: 8534962 [TBL] [Abstract][Full Text] [Related]
29. Identification of the gene responsible for the cblA complementation group of vitamin B12-responsive methylmalonic acidemia based on analysis of prokaryotic gene arrangements. Dobson CM; Wai T; Leclerc D; Wilson A; Wu X; Doré C; Hudson T; Rosenblatt DS; Gravel RA Proc Natl Acad Sci U S A; 2002 Nov; 99(24):15554-9. PubMed ID: 12438653 [TBL] [Abstract][Full Text] [Related]
30. 14C-propionate incorporation assay by rapid filtration in multiwell plates. Kakinuma H; Kobayashi A; Takahashi H Clin Chim Acta; 2004 May; 343(1-2):209-12. PubMed ID: 15115697 [TBL] [Abstract][Full Text] [Related]
31. Transcobalamin II deficiency with methylmalonic aciduria in three sisters. Bibi H; Gelman-Kohan Z; Baumgartner ER; Rosenblatt DS J Inherit Metab Dis; 1999 Oct; 22(7):765-72. PubMed ID: 10518276 [TBL] [Abstract][Full Text] [Related]
32. Impact of cblB mutations on the function of ATP:cob(I)alamin adenosyltransferase in disorders of vitamin B12 metabolism. Zhang J; Dobson CM; Wu X; Lerner-Ellis J; Rosenblatt DS; Gravel RA Mol Genet Metab; 2006 Apr; 87(4):315-22. PubMed ID: 16439175 [TBL] [Abstract][Full Text] [Related]
33. [Combined methylmalonic acidemia and homocystinuria; a case report]. Jiménez Varo I; Bueno Delgado M; Dios Fuentes E; Delgado Pecellin C; González Meneses A; Soto Moreno A; Venegas Moreno E Nutr Hosp; 2015 Apr; 31(4):1885-8. PubMed ID: 25795986 [TBL] [Abstract][Full Text] [Related]
34. Failure of lysosomal release of vitamin B12: a new complementation group causing methylmalonic aciduria (cblF). Watkins D; Rosenblatt DS Am J Hum Genet; 1986 Sep; 39(3):404-8. PubMed ID: 3766542 [TBL] [Abstract][Full Text] [Related]