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5. Congenital defect in intracellular cobalamin metabolism resulting in homocysteinuria and methylmalonic aciduria. I. Case report and histopathology. Baumgartner ER; Wick H; Maurer R; Egli N; Steinmann B Helv Paediatr Acta; 1979; 34(5):465-82. PubMed ID: 528229 [TBL] [Abstract][Full Text] [Related]
6. Homocystinuria and megaloblastic anemia responsive to vitamin B12 therapy. An inborn error of metabolism due to a defect in cobalamin metabolism. Schuh S; Rosenblatt DS; Cooper BA; Schroeder ML; Bishop AJ; Seargeant LE; Haworth JC N Engl J Med; 1984 Mar; 310(11):686-90. PubMed ID: 6700644 [TBL] [Abstract][Full Text] [Related]
7. Inborn errors of cobalamin absorption and metabolism. Watkins D; Rosenblatt DS Am J Med Genet C Semin Med Genet; 2011 Feb; 157C(1):33-44. PubMed ID: 21312325 [TBL] [Abstract][Full Text] [Related]
8. Inherited defects of B12 metabolism. Mahoney MJ; Rosenberg LE Am J Med; 1970 May; 48(5):584-93. PubMed ID: 4912932 [No Abstract] [Full Text] [Related]
10. Vitamin B12 in health and disease: part I--inherited disorders of function, absorption, and transport. Kapadia CR Gastroenterologist; 1995 Dec; 3(4):329-44. PubMed ID: 8775094 [TBL] [Abstract][Full Text] [Related]
11. Vitamin B12-responsive neonatal megaloblastic anemia and homocystinuria with associated reduced methionine synthase activity. Hallam LJ; Sawyer M; Clark AC; Van der Weyden MB Blood; 1987 Apr; 69(4):1128-33. PubMed ID: 3828532 [TBL] [Abstract][Full Text] [Related]
12. Acquired and inherited disorders of cobalamin and folate in children. Whitehead VM Br J Haematol; 2006 Jul; 134(2):125-36. PubMed ID: 16846473 [TBL] [Abstract][Full Text] [Related]
13. Mechanism of vitamin B12-responsiveness in cblC methylmalonic aciduria with homocystinuria. Froese DS; Zhang J; Healy S; Gravel RA Mol Genet Metab; 2009 Dec; 98(4):338-43. PubMed ID: 19700356 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. Abnormal deoxyuridine suppression test in congenital methylmalonic aciduria-homocystinuria without megaloblastic anemia: divergent biochemical and morphological bone marrow manifestations of disordered cobalamin metabolism in man. Carmel R; Goodman SI Blood; 1982 Feb; 59(2):306-11. PubMed ID: 7055641 [TBL] [Abstract][Full Text] [Related]
18. A syndrome of methylmalonic aciduria, homocystinuria, megaloblastic anemia and neurologic abnormalities in a vitamin B12-deficient breast-fed infant of a strict vegetarian. Higginbottom MC; Sweetman L; Nyhan WL N Engl J Med; 1978 Aug; 299(7):317-23. PubMed ID: 683264 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. Cobalamin deficiency and related disorders in infancy and childhood. Matthews DM; Linnell JC Eur J Pediatr; 1982 Feb; 138(1):6-16. PubMed ID: 7042350 [No Abstract] [Full Text] [Related] [Next] [New Search]