115 related articles for article (PubMed ID: 25314)
1. Severe hyperammonemia in a newborn infant with methylmalonyl-CoA mutase deficiency.
Packman S; Mahoney MJ; Tanaka K; Hsia YE
J Pediatr; 1978 May; 92(5):769-71. PubMed ID: 25314
[No Abstract] [Full Text] [Related]
2. Methylmalonyl-CoA mutase deficiency associated with severe neonatal hyperammonemia: activity of urea cycle enzymes.
Shapiro LJ; Bocian ME; Raijman L; Cederbaum SD; Shaw KN
J Pediatr; 1978 Dec; 93(6):986-8. PubMed ID: 31423
[No Abstract] [Full Text] [Related]
3. Methylmalonic acidemia.
Matsuda I; Terashima T; Yamamoto J; Akaboshi I; Shinozuka S; Hattori S; Nagata N; Oka Y
Eur J Pediatr; 1978 Jul; 128(3):181-6. PubMed ID: 27367
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. [Hyperammonemia in childhood. II. Enzymopathies not related to the urea cycle].
Kopieczna-Grzebieniak E; Toborek M; Jakubowska D; Tarnawski R
Pediatr Pol; 1988 Feb; 63(2):129-36. PubMed ID: 2900490
[No Abstract] [Full Text] [Related]
6. A new variant of methylmalonic acidemia-defective coenzyme-apoenzyme binding in cultured fibroblasts.
Morrow G; Revsin B; Clark R; Lebowitz J; Whelan DT
Clin Chim Acta; 1978 Apr; 85(1):67-72. PubMed ID: 25730
[TBL] [Abstract][Full Text] [Related]
7. Benign methylmalonic aciduria.
Ledley FD; Levy HL; Shih VE; Benjamin R; Mahoney MJ
N Engl J Med; 1984 Oct; 311(16):1015-8. PubMed ID: 6148691
[TBL] [Abstract][Full Text] [Related]
8. Studies of methylmalonyl-coenzyme A carbonylmutase activity in methylmalonic acidemia. II. In vitro binding kinetics with adenosylcobalamin.
Morrow G; Lebowitz J
Biochem Med; 1976 Jun; 15(3):241-5. PubMed ID: 11786
[No Abstract] [Full Text] [Related]
9. A case of methylmalonic and propionic acidemia due to methulmalonyl-CoA carbonylmutase apoenzyme deficiency.
van den Berg H; Boelkens MT; Hommes FA
Acta Paediatr Scand; 1976 Jan; 65(1):113-8. PubMed ID: 3087
[TBL] [Abstract][Full Text] [Related]
10. Methylmalonic aciduria: a variant form of methylmalonyl coenzyme A apomutase deficiency.
Wilcken B; Kilham HA; Faull K
J Pediatr; 1977 Sep; 91(3):428-30. PubMed ID: 19569
[TBL] [Abstract][Full Text] [Related]
11. Immunochemical studies on cultured fibroblasts from patients with inherited methylmalonic acidemia.
Kolhouse JF; Utley C; Fenton WA; Rosenberg LE
Proc Natl Acad Sci U S A; 1981 Dec; 78(12):7737-41. PubMed ID: 6121323
[TBL] [Abstract][Full Text] [Related]
12. [Isolated methylmalonyl-CoA mutase deficiency].
Yoshino M
Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):269-72. PubMed ID: 9590044
[No Abstract] [Full Text] [Related]
13. Methylmalonyl-CoA mutase activity of leukocytes in variants and heterozygotes of methylmalonic acidemia.
Narisawa K; Saito T; Hisa S; Suzuki H; Hayasaka K
Tohoku J Exp Med; 1977 Sep; 123(1):1-8. PubMed ID: 21471
[TBL] [Abstract][Full Text] [Related]
14. Novel mutation of methylmalonyl-CoA mutase gene causing the mut0 form of methylmalonic acidemia in a Japanese girl.
Oyama C; Takahashi T; Matsumori M; Shoji Y; Tajima G; Sakura N; Hasegawa Y; Yamaguchi S; Kakinuma H; Takada G
Pediatr Int; 2007 Apr; 49(2):232-4. PubMed ID: 17445044
[No Abstract] [Full Text] [Related]
15. Screening for methylmalonic aciduria in Alberta: a voluntary program with particular significance for the Hutterite Brethren.
Fowlow SB; Holmes TM; Morgan K; Snyder FF
Am J Med Genet; 1985 Nov; 22(3):513-9. PubMed ID: 2865895
[TBL] [Abstract][Full Text] [Related]
16. Inherited deficiencies of human methylmalonyl CaA mutase activity: reduced affinity of mutant apoenzyme for adenosylcobalamin.
Willard HF; Rosenberg LE
Biochem Biophys Res Commun; 1977 Oct; 78(3):927-34. PubMed ID: 20894
[No Abstract] [Full Text] [Related]
17. Genetic complementation among inherited deficiencies of methylmalonyl-CoA mutase activity: evidence for a new class of human cobalamin mutant.
Willard HF; Mellman IS; Rosenberg LE
Am J Hum Genet; 1978 Jan; 30(1):1-13. PubMed ID: 23678
[No Abstract] [Full Text] [Related]
18. Studies of methylmalonyl coenzyme A carbonylmutase activity in methylmalonic acidemia. I. Correlation of clinical, hepatic, and fibroblast data.
Morrow G; Mahoney MJ; Mathews C; Lebowitz J
Pediatr Res; 1975 Aug; 9(8):641-4. PubMed ID: 239382
[TBL] [Abstract][Full Text] [Related]
19. Immunochemical studies of fibroblasts from patients with methylmalonyl-CoA mutase apoenzyme deficiency: detection of a mutation interfering with mitochondrial import.
Fenton WA; Hack AM; Kraus JP; Rosenberg LE
Proc Natl Acad Sci U S A; 1987 Mar; 84(5):1421-4. PubMed ID: 2881300
[TBL] [Abstract][Full Text] [Related]
20. [Molecular diagnosis of a kindred with novel mutation of methylmalonyl-CoA mutase gene using non-RI SSCP].
Toyo-Oka Y; Wada C; Ohnuki Y; Takada F; Ohtani H
Rinsho Byori; 1995 Jun; 43(6):625-9. PubMed ID: 7602808
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
