110 related articles for article (PubMed ID: 7140596)
1. [Methylmalonic aciduria].
Similä S; Ruokonen A; Palotie A; Ruostesuo J; Puukka M
Duodecim; 1982; 98(18):1332-7. PubMed ID: 7140596
[No Abstract] [Full Text] [Related]
2. Malonyl coenzyme A decarboxylase deficiency.
Brown GK; Scholem RD; Bankier A; Danks DM
J Inherit Metab Dis; 1984; 7(1):21-6. PubMed ID: 6145813
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Prenatal diagnosis of methylmalonic aciduria.
Gompertz D; Goodey PA; Saudubray JM; Charpentier C; Chignolle A; Girard S
Pediatrics; 1974 Oct; 54(4):511-3. PubMed ID: 4415169
[No Abstract] [Full Text] [Related]
5. Methylmalonyl coenzyme A racemase defect: another cause of methylmalonic aciduria.
Kang ES; Snodgrass PJ; Gerald PS
Pediatr Res; 1972 Dec; 6(12):875-9. PubMed ID: 4643536
[No Abstract] [Full Text] [Related]
6. Methylmalonic aciduria. A newly discovered inborn error.
Barness LA; Morrow G
Ann Intern Med; 1968 Sep; 69(3):633-5. PubMed ID: 5673182
[No Abstract] [Full Text] [Related]
7. A rapid screening test for the detection of congenital methylmalonic aciduria in infancy.
Giorgio AJ; Luhby AL
Tech Bull Regist Med Technol; 1969 Aug; 39(8):180-5. PubMed ID: 5797889
[No Abstract] [Full Text] [Related]
8. Massachusetts Metabolic Disorders Screening Program. II. Methylmalonic aciduria.
Coulombe JT; Shih VE; Levy HL
Pediatrics; 1981 Jan; 67(1):26-31. PubMed ID: 7243433
[TBL] [Abstract][Full Text] [Related]
9. Sudden infant death syndrome and multiple acyl-coenzyme A dehydrogenase deficiency, ethylmalonic-adipic aciduria, or systemic carnitine deficiency.
Harpey JP; Charpentier C; Coudé M; Divry P; Paturneau-Jouas M
J Pediatr; 1987 Jun; 110(6):881-4. PubMed ID: 3585604
[No Abstract] [Full Text] [Related]
10. [Methylmalonic aciduria].
Kastrup KW
Ugeskr Laeger; 1968 Jun; 130(25):1054-5. PubMed ID: 5704253
[No Abstract] [Full Text] [Related]
11. 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]
12. The utilization of methylmalonyl-CoA for branched-chain fatty-acid synthesis by preparations from bovine (Bos taurus) adipose tissue.
Wahle KW; Paterson SM
Int J Biochem; 1979; 10(5):433-7. PubMed ID: 478105
[No Abstract] [Full Text] [Related]
13. Combined malonic and methylmalonic aciduria with normal malonyl-coenzyme A decarboxylase activity: a case supporting multiple aetiologies.
Gregg AR; Warman AW; Thorburn DR; O'Brien WE
J Inherit Metab Dis; 1998 Jun; 21(4):382-90. PubMed ID: 9700595
[TBL] [Abstract][Full Text] [Related]
14. [Vitamin B 12 responsive methylmalenic aciduria. Apropos of a new case].
Sann L; Divry P; Rolland MO; Bourgeois J; Bethenod M
Pediatrie; 1980; 35(3):205-12. PubMed ID: 7393687
[No Abstract] [Full Text] [Related]
15. Metabolic response to carnitine in methylmalonic aciduria. An effective strategy for elimination of propionyl groups.
Roe CR; Hoppel CL; Stacey TE; Chalmers RA; Tracey BM; Millington DS
Arch Dis Child; 1983 Nov; 58(11):916-20. PubMed ID: 6651329
[TBL] [Abstract][Full Text] [Related]
16. Studies on cultured fibroblasts in a case of methylmalonic aciduria.
Davidson JS; Lloyd A; Christianson A; Harley EH; Berger GM
S Afr Med J; 1984 Feb; 65(7):257-60. PubMed ID: 6141644
[TBL] [Abstract][Full Text] [Related]
17. The use of neomycin in the treatment of methylmalonic aciduria.
Snyderman SE; Sansaricq C; Norton P; Phansalkar SV
Pediatrics; 1972 Dec; 50(6):925-7. PubMed ID: 4636459
[No Abstract] [Full Text] [Related]
18. 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]
19. 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]
20. Methylmalonic aciduria. An inborn error leading to metabolic acidosis, long-chain ketonuria and intermittent hyperglycinemia.
Rosenberg LE; Lilljeqvist AC; Hsia YE
N Engl J Med; 1968 Jun; 278(24):1319-22. PubMed ID: 5648598
[No Abstract] [Full Text] [Related]
[Next] [New Search]