132 related articles for article (PubMed ID: 7055641)
1. 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]
2. Congenital methylmalonic aciduria--homocystinuria with megaloblastic anemia: observations on response to hydroxocobalamin and on the effect of homocysteine and methionine on the deoxyuridine suppression test.
Carmel R; Bedros AA; Mace JW; Goodman SI
Blood; 1980 Apr; 55(4):570-9. PubMed ID: 7357085
[No Abstract] [Full Text] [Related]
3. 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]
4. Atypical cobalamin deficiency. Subtle biochemical evidence of deficiency is commonly demonstrable in patients without megaloblastic anemia and is often associated with protein-bound cobalamin malabsorption.
Carmel R; Sinow RM; Karnaze DS
J Lab Clin Med; 1987 Apr; 109(4):454-63. PubMed ID: 3819580
[TBL] [Abstract][Full Text] [Related]
5. Reversal by cobalamin therapy of minimal defects in the deoxyuridine suppression test in patients without anemia: further evidence for a subtle metabolic cobalamin deficiency.
Carmel R
J Lab Clin Med; 1992 Mar; 119(3):240-4. PubMed ID: 1541874
[TBL] [Abstract][Full Text] [Related]
6. In vitro DNA synthesis by megaloblastic bone marrow: effect of folates and cobalamins on thymidine incorporation and de novo thymidylate synthesis.
Das KC; Herbert V
Am J Hematol; 1989 May; 31(1):11-20. PubMed ID: 2705438
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Clinical heterogeneity in cobalamin C variant of combined homocystinuria and methylmalonic aciduria.
Mitchell GA; Watkins D; Melançon SB; Rosenblatt DS; Geoffroy G; Orquin J; Homsy MB; Dallaire L
J Pediatr; 1986 Mar; 108(3):410-5. PubMed ID: 3950820
[TBL] [Abstract][Full Text] [Related]
9. Cobalamin-dependent metabolism in chronic myelogenous leukemia determined by deoxyuridine suppression test and the formiminoglutamic acid and methylmalonate excretion in urine.
Gimsing P; Hippe E
Am J Hematol; 1995 Jun; 49(2):121-30. PubMed ID: 7771463
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. The deoxyuridine suppression test identifies subtle cobalamin deficiency in patients without typical megaloblastic anemia.
Carmel R; Karnaze DS
JAMA; 1985 Mar; 253(9):1284-7. PubMed ID: 3968853
[TBL] [Abstract][Full Text] [Related]
13. The effect of deoxyuridine, vitamin B12, folate and alcohol on the uptake of thymidine and on the deoxynucleoside triphosphate concentrations in normal and megaloblastic cells.
Ganeshaguru K; Hoffbrand AV
Br J Haematol; 1978 Sep; 40(1):29-41. PubMed ID: 309336
[TBL] [Abstract][Full Text] [Related]
14. Marrow cells from patients with untreated pernicious anaemia cannot use tetrahydrofolate normally.
Deacon R; Chanarin I; Perry J; Lumb M
Br J Haematol; 1980 Dec; 46(4):523-8. PubMed ID: 7437330
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. Deoxyuridine metabolism in human megaloblastic marrow cells.
Van Der Weyden MB
Scand J Haematol; 1979 Jul; 23(1):37-42. PubMed ID: 493870
[TBL] [Abstract][Full Text] [Related]
18. Minor facial anomalies in combined methylmalonic aciduria and homocystinuria due to a defect in cobalamin metabolism.
Cerone R; Schiaffino MC; Caruso U; Lupino S; Gatti R
J Inherit Metab Dis; 1999 May; 22(3):247-50. PubMed ID: 10384379
[No Abstract] [Full Text] [Related]
19. Biochemical diagnosis and outcome of 2 years treatment in a patient with combined methylmalonic aciduria and homocystinuria.
Bellini C; Cerone R; Bonacci W; Caruso U; Magliano CP; Serra G; Fowler B; Romano C
Eur J Pediatr; 1992 Nov; 151(11):818-20. PubMed ID: 1468456
[TBL] [Abstract][Full Text] [Related]
20. The effect of folate analogues and vitamin B12 on provision of thymine nucleotides for DNA synthesis in megaloblastic anemia.
Taheri MR; Wickremasinghe RG; Jackson BF; Hoffbrand AV
Blood; 1982 Mar; 59(3):634-40. PubMed ID: 6977386
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
