129 related articles for article (PubMed ID: 657530)
1. 3-Methylcrotonylglycine excretion in 3-hydroxy-3-methylglutaric aciduria.
Wysocki SJ; Hähnel R
Clin Chim Acta; 1978 May; 86(1):101-8. PubMed ID: 657530
[TBL] [Abstract][Full Text] [Related]
2. A combined defect of three mitochondrial carboxylases presenting as biotin-responsive 3-methylcrotonyl glycinuria and 3-hydroxyisovaleric aciduria.
Bartlett K; Ng H; Leonard JV
Clin Chim Acta; 1980 Jan; 100(2):183-6. PubMed ID: 6766095
[TBL] [Abstract][Full Text] [Related]
3. The urinary organic acid profile associated with 3-hydroxy-3-methylglutaric aciduria.
Faull KF; Bolton PD; Halpern B; Hammond J; Danks DM
Clin Chim Acta; 1976 Dec; 73(3):553-9. PubMed ID: 1000872
[No Abstract] [Full Text] [Related]
4. Glutaric aciduria Type II.
Sweetman L; Nyhan WL; Tauner DA; Merritt TA; Singh M
J Pediatr; 1980 Jun; 96(6):1020-6. PubMed ID: 7373461
[TBL] [Abstract][Full Text] [Related]
5. 3-Hydroxy-3-methylglutaric aciduria: deficiency of 3-hydroxy-3-methylglutaryl coenzyme A lyase.
Wysocki SJ; Hähnel R
Clin Chim Acta; 1976 Sep; 71(2):349-51. PubMed ID: 963901
[TBL] [Abstract][Full Text] [Related]
6. 3-Hydroxy-3-methylglutaric aciduria, combined with 3-methylglutaconic aciduria.
Wysocki SJ; Wilkinson SP; Hähnel R; Wong CY; Panegyres PK
Clin Chim Acta; 1976 Aug; 70(3):399-406. PubMed ID: 947633
[TBL] [Abstract][Full Text] [Related]
7. Photodiode array detection for liquid chromatographic profiling of carboxylic acids in physiological fluids: 3-hydroxy-3-methylglutaric aciduria.
Buchanan DN; Thoene JG
Clin Chem; 1986 Jan; 32(1 Pt 1):169-71. PubMed ID: 2416490
[TBL] [Abstract][Full Text] [Related]
8. L-2-Hydroxyglutaric aciduria: an inborn error of metabolism?
Duran M; Kamerling JP; Bakker HD; van Gennip AH; Wadman SK
J Inherit Metab Dis; 1980; 3(4):109-12. PubMed ID: 6787330
[TBL] [Abstract][Full Text] [Related]
9. A neonatal case of 3-hydroxy-3-methylglutaric-coenzyme A lyase deficiency.
Santarelli F; Cassanello M; Enea A; Poma F; D'Onofrio V; Guala G; Garrone G; Puccinelli P; Caruso U; Porta F; Spada M
Ital J Pediatr; 2013 May; 39():33. PubMed ID: 23705938
[TBL] [Abstract][Full Text] [Related]
10. Potential misdiagnosis of 3-methylcrotonyl-coenzyme A carboxylase deficiency associated with absent or trace urinary 3-methylcrotonylglycine.
Wolfe LA; Finegold DN; Vockley J; Walters N; Chambaz C; Suormala T; Koch HG; Matern D; Barshop BA; Cropcho LJ; Baumgartner MR; Gibson KM
Pediatrics; 2007 Nov; 120(5):e1335-40. PubMed ID: 17908719
[TBL] [Abstract][Full Text] [Related]
11. Organic acidurias: approach, results and clinical relevance.
Wadman SK; Duran M; Kamerling JP
Ciba Found Symp; 1982; 87():324-39. PubMed ID: 6918293
[TBL] [Abstract][Full Text] [Related]
12. Massive excretion of 2-oxoglutaric acid and 3-hydroxyisovaleric acid in a patient with a deficiency of 3-methylcrotonyl-CoA carboxylase.
Finnie MD; Cottrall K; Seakins JW; Snedden W
Clin Chim Acta; 1976 Dec; 73(3):513-9. PubMed ID: 1000869
[TBL] [Abstract][Full Text] [Related]
13. L-2-Hydroxyglutaric aciduria presenting as status epilepticus.
Zafeiriou DI; Sewell A; Savvopoulou-Augoustidou P; Gombakis N; Katzos G
Brain Dev; 2001 Jul; 23(4):255-7. PubMed ID: 11377007
[TBL] [Abstract][Full Text] [Related]
14. A method for the determination of volatile organic acids in aqueous solutions and urine, and the results obtained in propionic acidaemia, beta-methylcrotonylglycinuria and methylmalonic aciduria.
Chalmers RA; Bickle S; Watts RW
Clin Chim Acta; 1974 Mar; 52(1):31-41. PubMed ID: 4827457
[No Abstract] [Full Text] [Related]
15. Glutaric aciduria; presence of glutaconic and beta-hydroxyglutaric acids in urine.
Stokke O; Goodman SI; Thompson JA; Miles BS
Biochem Med; 1975 Apr; 12(4):386-91. PubMed ID: 1164416
[No Abstract] [Full Text] [Related]
16. Beta-methylcrotonic aciduria associated with lactic acidosis.
Roth K; Cohn R; Yandrasitz J; Preti G; Dodd P; Segal S
J Pediatr; 1976 Feb; 88(2):229-35. PubMed ID: 1249684
[TBL] [Abstract][Full Text] [Related]
17. Evaluation of urinary acylglycines by electrospray tandem mass spectrometry in mitochondrial energy metabolism defects and organic acidurias.
Bonafé L; Troxler H; Kuster T; Heizmann CW; Chamoles NA; Burlina AB; Blau N
Mol Genet Metab; 2000 Apr; 69(4):302-11. PubMed ID: 10870848
[TBL] [Abstract][Full Text] [Related]
18. A case of 3-methylglutaconic aciduria misdiagnosed as cerebral palsy.
Pantaleoni C; D'Arrigo S; D'Incerti L; Rimoldi M; Riva D
Pediatr Neurol; 2000 Nov; 23(5):442-4. PubMed ID: 11118804
[TBL] [Abstract][Full Text] [Related]
19. Glycine and L-carnitine therapy in 3-methylcrotonyl-CoA carboxylase deficiency.
Rutledge SL; Berry GT; Stanley CA; van Hove JL; Millington D
J Inherit Metab Dis; 1995; 18(3):299-305. PubMed ID: 7474896
[TBL] [Abstract][Full Text] [Related]
20. Inherited 3-methylglutaconic aciduria in two brothers--another defect of leucine metabolism.
Duran M; Beemer FA; Tibosch AS; Bruinvis L; Ketting D; Wadman SK
J Pediatr; 1982 Oct; 101(4):551-4. PubMed ID: 6181239
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
