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5. 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]
10. The detection of 3-methylglutarylcarnitine and a new dicarboxylic conjugate, 3-methylglutaconylcarnitine, in 3-methylglutaconic aciduria. Jooste S; Erasmus E; Mienie LJ; de Wet WJ; Gibson KM Clin Chim Acta; 1994 Oct; 230(1):1-8. PubMed ID: 7850987 [TBL] [Abstract][Full Text] [Related]
11. 3-Methylglutaconic aciduria: a new metabolic disorder associated with early onset optic atrophy. Kesler A; Gadoth N; Straussberg R J Neuroophthalmol; 1997 Dec; 17(4):278-9. PubMed ID: 9427184 [No Abstract] [Full Text] [Related]
13. 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]
14. 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]
15. 3-Methylglutaconic aciduria with persistent metabolic acidosis and 'uncoupling episodes'. Elpeleg ON; Meiron D; Barash V; Hurwitz Y; Tal I; Amir N J Inherit Metab Dis; 1990; 13(2):235-6. PubMed ID: 2116558 [No Abstract] [Full Text] [Related]
16. 3-Methylglutaconic aciduria type I: clinical heterogeneity as a neurometabolic disease. Shoji Y; Takahashi T; Sawaishi Y; Ishida A; Matsumori M; Shoji Y; Enoki M; Watanabe H; Takada G J Inherit Metab Dis; 1999 Feb; 22(1):1-8. PubMed ID: 10070612 [TBL] [Abstract][Full Text] [Related]