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27. Basolateral-membrane transport defect for lysine in lysinuric protein intolerance. Rajantie J; Simell O; Perheentupa J Lancet; 1980 Jun; 1(8180):1219-21. PubMed ID: 6104037 [TBL] [Abstract][Full Text] [Related]
28. [Progress of glutaric aciduria type I]. Gao JZ; Luo XP Zhonghua Er Ke Za Zhi; 2012 Dec; 50(12):912-4. PubMed ID: 23324148 [No Abstract] [Full Text] [Related]
30. New insights into human lysine degradation pathways with relevance to pyridoxine-dependent epilepsy due to antiquitin deficiency. Crowther LM; Mathis D; Poms M; Plecko B J Inherit Metab Dis; 2019 Jul; 42(4):620-628. PubMed ID: 30767241 [TBL] [Abstract][Full Text] [Related]
32. Alpha-ketoadipic aciduria: a description of a new metabolic error in lysine-tryptophan degradation. Wilson RW; Wilson CM; Gates SC; Higgins JV Pediatr Res; 1975 Jun; 9(6):522-6. PubMed ID: 1161338 [TBL] [Abstract][Full Text] [Related]
33. Glutaric acidemia type 1 in patients of Lumbee heritage from North Carolina. Basinger AA; Booker JK; Frazier DM; Koeberl DD; Sullivan JA; Muenzer J Mol Genet Metab; 2006 May; 88(1):90-2. PubMed ID: 16466958 [TBL] [Abstract][Full Text] [Related]
34. [Glutaric aciduria type 1: an example of the importance of early detection of so-called cerebral organic aciduria]. Barić I; Baraka K; Maradin M; Bartonicek D; Sarnavka V; Begović D; Fumić K Lijec Vjesn; 2003; 125(11-12):312-6. PubMed ID: 15209027 [TBL] [Abstract][Full Text] [Related]
35. Aminoacidurias due to inherited disorders of metabolism. 2. Frimpter GW N Engl J Med; 1973 Oct; 289(17):895-901. PubMed ID: 4598151 [No Abstract] [Full Text] [Related]
37. A case of hyperlysinemia: biochemical and clinical observations. Armstrong MD; Robinow M Pediatrics; 1967 Apr; 39(4):546-54. PubMed ID: 6022933 [No Abstract] [Full Text] [Related]