143 related articles for article (PubMed ID: 2203337)
1. Inherited disorders of vitamin B12 utilization.
Rosenblatt DS; Cooper BA
Bioessays; 1990 Jul; 12(7):331-4. PubMed ID: 2203337
[TBL] [Abstract][Full Text] [Related]
2. Prenatal diagnosis for methylmalonic acidemia and inborn errors of vitamin B12 metabolism and transport.
Morel CF; Watkins D; Scott P; Rinaldo P; Rosenblatt DS
Mol Genet Metab; 2005; 86(1-2):160-71. PubMed ID: 16150626
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. Congenital defect in intracellular cobalamin metabolism resulting in homocystinuria and methylmalonic aciduria. II. Biochemical investigations.
Baumgartner ER; Wick H; Linnell JC; Gaull GE; Bachmann C; Steinmann B
Helv Paediatr Acta; 1979; 34(5):483-96. PubMed ID: 43301
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. New disorder of vitamin B12 metabolism (cobalamin F) presenting as methylmalonic aciduria.
Rosenblatt DS; Laframboise R; Pichette J; Langevin P; Cooper BA; Costa T
Pediatrics; 1986 Jul; 78(1):51-4. PubMed ID: 3725502
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Combined methylmalonic aciduria and homocystinuria (cblC): phenotype-genotype correlations and ethnic-specific observations.
Morel CF; Lerner-Ellis JP; Rosenblatt DS
Mol Genet Metab; 2006 Aug; 88(4):315-21. PubMed ID: 16714133
[TBL] [Abstract][Full Text] [Related]
10. Mutation and biochemical analysis of patients belonging to the cblB complementation class of vitamin B12-dependent methylmalonic aciduria.
Lerner-Ellis JP; Gradinger AB; Watkins D; Tirone JC; Villeneuve A; Dobson CM; Montpetit A; Lepage P; Gravel RA; Rosenblatt DS
Mol Genet Metab; 2006 Mar; 87(3):219-25. PubMed ID: 16410054
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Functional methionine synthase deficiency (cblE and cblG): clinical and biochemical heterogeneity.
Watkins D; Rosenblatt DS
Am J Med Genet; 1989 Nov; 34(3):427-34. PubMed ID: 2688421
[TBL] [Abstract][Full Text] [Related]
13. Complementation studies in the cblA class of inborn error of cobalamin metabolism: evidence for interallelic complementation and for a new complementation class (cblH).
Watkins D; Matiaszuk N; Rosenblatt DS
J Med Genet; 2000 Jul; 37(7):510-3. PubMed ID: 10882753
[TBL] [Abstract][Full Text] [Related]
14. [Vitamin B12 and related genetic disorders].
Guéant JL; Coelho D; Nicolas JP
Bull Acad Natl Med; 2014 Jun; 198(6):1141-56. PubMed ID: 26983191
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Mitochondrial vitamin B12-binding proteins in patients with inborn errors of cobalamin metabolism.
Moras E; Hosack A; Watkins D; Rosenblatt DS
Mol Genet Metab; 2007 Feb; 90(2):140-7. PubMed ID: 17011224
[TBL] [Abstract][Full Text] [Related]
17. Clinical and molecular heterogeneity in patients with the cblD inborn error of cobalamin metabolism.
Miousse IR; Watkins D; Coelho D; Rupar T; Crombez EA; Vilain E; Bernstein JA; Cowan T; Lee-Messer C; Enns GM; Fowler B; Rosenblatt DS
J Pediatr; 2009 Apr; 154(4):551-6. PubMed ID: 19058814
[TBL] [Abstract][Full Text] [Related]
18. Genetic defects of cobalamin metabolism.
Rennert OM
Ann Clin Lab Sci; 1980; 10(4):356-60. PubMed ID: 7447389
[TBL] [Abstract][Full Text] [Related]
19. Neuropsychiatric disturbances in presumed late-onset cobalamin C disease.
Roze E; Gervais D; Demeret S; Ogier de Baulny H; Zittoun J; Benoist JF; Said G; Pierrot-Deseilligny C; Bolgert F
Arch Neurol; 2003 Oct; 60(10):1457-62. PubMed ID: 14568819
[TBL] [Abstract][Full Text] [Related]
20. Altered vitamin B12 metabolism in fibroblasts from a patient with megaloblastic anemia and homocystinuria due to a new defect in methionine biosynthesis.
Rosenblatt DS; Cooper BA; Pottier A; Lue-Shing H; Matiaszuk N; Grauer K
J Clin Invest; 1984 Dec; 74(6):2149-56. PubMed ID: 6511919
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]