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3. 3-Methylglutaconic and 3-methylglutaric aciduria in a patient with suspected 3-methylglutaconyl-CoA hydratase deficiency. Lehnert W; Scharf J; Wendel U Eur J Pediatr; 1985 Mar; 143(4):301-3. PubMed ID: 2580710 [TBL] [Abstract][Full Text] [Related]
4. 3-Methylglutaconic aciduria: a new variant. Zeharia A; Elpeleg ON; Mukamel M; Weitz R; Ariel R; Mimouni M Pediatrics; 1992 Jun; 89(6 Pt 1):1080-2. PubMed ID: 1594352 [TBL] [Abstract][Full Text] [Related]
5. Type IV 3-methylglutaconic (3-MGC) aciduria: a new case presenting with hepatic dysfunction. Broide E; Elpeleg O; Lahat E Pediatr Neurol; 1997 Nov; 17(4):353-5. PubMed ID: 9436802 [TBL] [Abstract][Full Text] [Related]
6. 3-Methylglutaconic aciduria: a phenotype in which activity of 3-methylglutaconyl-coenzyme A hydratase is normal. Gibson KM; Nyhan WL; Sweetman L; Narisawa K; Lehnert W; Divry P; Robinson BH; Roth KS; Beemer FA; van Sprang FJ Eur J Pediatr; 1988 Oct; 148(1):76-82. PubMed ID: 3197737 [TBL] [Abstract][Full Text] [Related]
7. 3-Methylglutaconic aciduria--lessons from 50 genes and 977 patients. Wortmann SB; Kluijtmans LA; Rodenburg RJ; Sass JO; Nouws J; van Kaauwen EP; Kleefstra T; Tranebjaerg L; de Vries MC; Isohanni P; Walter K; Alkuraya FS; Smuts I; Reinecke CJ; van der Westhuizen FH; Thorburn D; Smeitink JA; Morava E; Wevers RA J Inherit Metab Dis; 2013 Nov; 36(6):913-21. PubMed ID: 23355087 [TBL] [Abstract][Full Text] [Related]
8. Association of 3-methylglutaconic aciduria with sensori-neural deafness, encephalopathy, and Leigh-like syndrome (MEGDEL association) in four patients with a disorder of the oxidative phosphorylation. Wortmann S; Rodenburg RJ; Huizing M; Loupatty FJ; de Koning T; Kluijtmans LA; Engelke U; Wevers R; Smeitink JA; Morava E Mol Genet Metab; 2006 May; 88(1):47-52. PubMed ID: 16527507 [TBL] [Abstract][Full Text] [Related]
9. 3-Methylglutaconic aciduria: ten new cases with a possible new phenotype. al Aqeel A; Rashed M; Ozand PT; Brismar J; Gascon GG; al Odaib A; Dabbagh O Brain Dev; 1994 Nov; 16 Suppl():23-32. PubMed ID: 7726378 [TBL] [Abstract][Full Text] [Related]
10. Mutations in the AUH gene cause 3-methylglutaconic aciduria type I. Ly TB; Peters V; Gibson KM; Liesert M; Buckel W; Wilcken B; Carpenter K; Ensenauer R; Hoffmann GF; Mack M; Zschocke J Hum Mutat; 2003 Apr; 21(4):401-7. PubMed ID: 12655555 [TBL] [Abstract][Full Text] [Related]
11. Inborn errors of metabolism with 3-methylglutaconic aciduria as discriminative feature: proper classification and nomenclature. Wortmann SB; Duran M; Anikster Y; Barth PG; Sperl W; Zschocke J; Morava E; Wevers RA J Inherit Metab Dis; 2013 Nov; 36(6):923-8. PubMed ID: 23296368 [TBL] [Abstract][Full Text] [Related]
12. 3-methylglutaconic aciduria type I in a boy with fever-associated seizures. Illsinger S; Lücke T; Zschocke J; Gibson KM; Das AM Pediatr Neurol; 2004 Mar; 30(3):213-5. PubMed ID: 15033206 [TBL] [Abstract][Full Text] [Related]
14. Deficiency of 3-methylglutaconyl-coenzyme A hydratase in two siblings with 3-methylglutaconic aciduria. Narisawa K; Gibson KM; Sweetman L; Nyhan WL; Duran M; Wadman SK J Clin Invest; 1986 Apr; 77(4):1148-52. PubMed ID: 3082934 [TBL] [Abstract][Full Text] [Related]
15. Multiple respiratory chain abnormalities associated with hypertrophic cardiomyopathy and 3-methylglutaconic aciduria. Ibel H; Endres W; Hadorn HB; Deufel T; Paetzke I; Duran M; Kennaway NG; Gibson KM Eur J Pediatr; 1993 Aug; 152(8):665-70. PubMed ID: 7691603 [TBL] [Abstract][Full Text] [Related]
16. Episodes of severe metabolic acidosis in a patient with 3-methylglutaconic aciduria. Haan EA; Scholem RD; Pitt JJ; Wraith JE; Brown GK Eur J Pediatr; 1987 Sep; 146(5):484-8. PubMed ID: 2445577 [TBL] [Abstract][Full Text] [Related]
17. 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]
18. Maternal 3-methylglutaconic aciduria associated with abnormalities in offspring. de Koning Tj; Duran M; Dorland L; Berger R; Poll-The BT Lancet; 1996 Sep; 348(9031):887-8. PubMed ID: 8826820 [No Abstract] [Full Text] [Related]
19. 3-Methylglutaconic aciduria: a marker for as yet unspecified disorders and the relevance of prenatal diagnosis in a 'new' type ('type 4'). Chitayat D; Chemke J; Gibson KM; Mamer OA; Kronick JB; McGill JJ; Rosenblatt B; Sweetman L; Scriver CR J Inherit Metab Dis; 1992; 15(2):204-12. PubMed ID: 1382150 [TBL] [Abstract][Full Text] [Related]