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27. Gene identification for the cblD defect of vitamin B12 metabolism. Coelho D; Suormala T; Stucki M; Lerner-Ellis JP; Rosenblatt DS; Newbold RF; Baumgartner MR; Fowler B N Engl J Med; 2008 Apr; 358(14):1454-64. PubMed ID: 18385497 [TBL] [Abstract][Full Text] [Related]
28. 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]
29. Vitamin B12: an area of darkness. Matthews DM; Linnell JC Br Med J; 1979 Sep; 2(6189):533-5. PubMed ID: 497676 [No Abstract] [Full Text] [Related]
30. [Biosynthesis of cobalamin coenzymes in tumor and hematopoietic tissues in assessing methotrexate sensitivity]. Miasishcheva NV; Vares IuV; Golenko OD; Nikolaeva TG Vestn Akad Med Nauk SSSR; 1986; (5):36-41. PubMed ID: 3727783 [No Abstract] [Full Text] [Related]
31. [Vitamin B 12 responsive methylmalenic aciduria. Apropos of a new case]. Sann L; Divry P; Rolland MO; Bourgeois J; Bethenod M Pediatrie; 1980; 35(3):205-12. PubMed ID: 7393687 [No Abstract] [Full Text] [Related]
32. Novel splice site mutations and a large deletion in three patients with the cblF inborn error of vitamin B12 metabolism. Miousse IR; Watkins D; Rosenblatt DS Mol Genet Metab; 2011 Apr; 102(4):505-7. PubMed ID: 21303734 [TBL] [Abstract][Full Text] [Related]
33. Gene discovery in methylmalonic aciduria and homocystinuria. Thiele J; Van Raamsdonk JM Clin Genet; 2006 May; 69(5):402-3. PubMed ID: 16650077 [No Abstract] [Full Text] [Related]
34. Cobalamin C disease presenting with hemophagocytic lymphohistiocytosis. Wu S; Gonzalez-Gomez I; Coates T; Yano S Pediatr Hematol Oncol; 2005 Dec; 22(8):717-21. PubMed ID: 16251179 [TBL] [Abstract][Full Text] [Related]
35. Methylmalonic acid excretion in methylmalonic acidemia. Kelly S; Cowger M N Y State J Med; 1980 Feb; 80(2):240-3. PubMed ID: 6929423 [No Abstract] [Full Text] [Related]
36. The dietary treatment of inborn errors of metabolism. Woolf LI Proc Nutr Soc; 1976 May; 35(1):31-6. PubMed ID: 781683 [No Abstract] [Full Text] [Related]
38. Cobalamin C mutation (methylmalonic aciduria and homocystinuria) in adolescence. A treatable cause of dementia and myelopathy. Shinnar S; Singer HS N Engl J Med; 1984 Aug; 311(7):451-4. PubMed ID: 6749192 [No Abstract] [Full Text] [Related]
39. Cobalamins and folates as seen through inborn errors of metabolism: a review and perspective. Haurani FI Vitam Horm; 2000; 60():353-81. PubMed ID: 11037629 [No Abstract] [Full Text] [Related]