222 related articles for article (PubMed ID: 5686220)
21. Studies on vitamin B12 metabolism in HeLa cells.
Kerwar SS; Spears C; McAuslan B; Weissbach H
Arch Biochem Biophys; 1971 Jan; 142(1):231-7. PubMed ID: 5545478
[No Abstract] [Full Text] [Related]
22. Methylmalonic/beta-hydroxy-n-valeric aciduria due to methylmalonyl-CoA mutase deficiency.
Goodman SI; McCabe ER; Fennessey PV; Miles BS; Mace JW; Jellum E
Clin Chim Acta; 1978 Aug; 87(3):441-9. PubMed ID: 28187
[TBL] [Abstract][Full Text] [Related]
23. Methylmalonic aciduria with homocystinuria: biochemical studies, treatment, and clinical course of a Cbl-C patient.
Ribes A; Briones P; Vilaseca MA; Lluch M; Rodes M; Maya A; Campistol J; Pascual P; Suormala T; Baumgartner R
Eur J Pediatr; 1990 Mar; 149(6):412-5. PubMed ID: 2332011
[TBL] [Abstract][Full Text] [Related]
24. Gluconeogenesis from propionate in kidney and liver of the vitamin B12-deficient rat.
Weidemann MJ; Hems R; Williams DL; Spray GH; Krebs HA
Biochem J; 1970 Mar; 117(1):177-81. PubMed ID: 5420952
[TBL] [Abstract][Full Text] [Related]
25. Possible interrelationship between vitamins E and b12 in the disturbance in methylmalonate metabolism in vitamin E deficiency.
Pappu AS; Fatterpaker P; Sreenivasan A
Biochem J; 1978 Apr; 172(1):115-21. PubMed ID: 656065
[TBL] [Abstract][Full Text] [Related]
26. Mental retardation, megaloblastic anaemia, methylmalonic aciduria and abnormal homocysteine metabolism due to an error in vitamin B12 metabolism.
Dillon MJ; England JM; Gompertz D; Goodey PA; Grant DB; Hussein HA; Linnell JC; Matthews DM; Mudd SH; Newns GH; Seakins JW; Uhlendorf BW; Wise IJ
Clin Sci Mol Med; 1974 Jul; 47(1):43-61. PubMed ID: 4853163
[No Abstract] [Full Text] [Related]
27. Vitamin B12-dependent methylmalonicaciduria: amino acid toxicity, long chain ketonuria, and protective effect of vitamin B12.
Hsia YE; Lilljeqvist AC; Rosenberg LE
Pediatrics; 1970 Oct; 46(4):497-507. PubMed ID: 5503685
[No Abstract] [Full Text] [Related]
28. Biochemical analysis of intact fibroblasts from two cases with methylmalonic acidaemia.
Kakinuma H; Ogura N; Ohtake A; Takayanagi M; Nakajima H; Kondo H; Terada H; Okuda K; Nomoto Y
J Inherit Metab Dis; 1985; 8(3):151-2. PubMed ID: 2879965
[No Abstract] [Full Text] [Related]
29. Prenatal therapy of a patient with vitamin-B12-responsive methylmalonic acidemia.
Ampola MG; Mahoney MJ; Nakamura E; Tanaka K
N Engl J Med; 1975 Aug; 293(7):313-7. PubMed ID: 239344
[TBL] [Abstract][Full Text] [Related]
30. [Methylmalonic acidemia].
Ohura T
Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):579-84. PubMed ID: 2908397
[No Abstract] [Full Text] [Related]
31. Genetic and biochemical analysis of human cobalamin mutants in cell culture.
Fenton WA; Rosenberg LE
Annu Rev Genet; 1978; 12():223-48. PubMed ID: 371525
[No Abstract] [Full Text] [Related]
32. Inborn errors of organic acid metabolism.
Gompertz D
Clin Endocrinol Metab; 1974 Mar; 3(1):107-30. PubMed ID: 4609643
[No Abstract] [Full Text] [Related]
33. A homozygous nonsense mutation in the methylmalonyl-CoA epimerase gene (MCEE) results in mild methylmalonic aciduria.
Bikker H; Bakker HD; Abeling NG; Poll-The BT; Kleijer WJ; Rosenblatt DS; Waterham HR; Wanders RJ; Duran M
Hum Mutat; 2006 Jul; 27(7):640-3. PubMed ID: 16752391
[TBL] [Abstract][Full Text] [Related]
34. Detection of inborn errors of metabolism. II. Defects in propionic acid metabolism.
Hill HZ; Goodman SI
Clin Genet; 1974; 6(2):73-8. PubMed ID: 4430155
[No Abstract] [Full Text] [Related]
35. B12-unresponsive methylmalonic aciduria in a female infant.
Vecchio F; Carnevale F; Paganetti G; di Bitonto G; Penza R; Francioso G
J Inherit Metab Dis; 1980; 3(3):91-2. PubMed ID: 6775146
[No Abstract] [Full Text] [Related]
36. [13C]Valine metabolism in methylmalonicacidemia using nuclear magnetic resonance: propinonate as an obligate intermediate.
Tanaka K; Armitage IM; Ramsdell HS; Hsia YE; Lipsky SR; Rosenberg LE
Proc Natl Acad Sci U S A; 1975 Sep; 72(9):3692-6. PubMed ID: 1059159
[TBL] [Abstract][Full Text] [Related]
37. A derangement in B 12 metabolism leading to homocystinemia, cystathioninemia and methylmalonic aciduria.
Mudd SH; Levy HL; Abeles RH; Jennedy JP
Biochem Biophys Res Commun; 1969 Apr; 35(1):121-6. PubMed ID: 5779140
[No Abstract] [Full Text] [Related]
38. Methylmalonyl CoA mutase--a radiochromatographic assay.
Goodey PA; Gompertz D
Clin Chim Acta; 1972 Nov; 42(1):119-23. PubMed ID: 4654847
[No Abstract] [Full Text] [Related]
39. Defective leukocyte metabolism in human cobalamin deficiency: impaired propionate oxidation and serine biosynthesis reversible by cyanocobalamin therapy.
Robertson JS; Hsia YE; Scully KJ
J Lab Clin Med; 1976 Jan; 87(1):89-97. PubMed ID: 1245786
[TBL] [Abstract][Full Text] [Related]
40. Rapid prenatal and postnatal detection of inborn errors of propionate, methylmalonate, and cobalamin metabolism: a sensitive assay using cultured cells.
Willard HF; Ambani LM; Hart AC; Mahoney MJ; Rosenberg LE
Hum Genet; 1976 Dec; 34(3):277-83. PubMed ID: 1002151
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
