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4. Familial hyperlysinaemia due to L-lysine alpha-ketoglutarate reductase deficiency: results of attempted treatment. vd Heiden C; Brink M; de Bree PK; v Sprang FJ; Wadman SK; de Pater JM; van Biervliet JP J Inherit Metab Dis; 1978; 1(3):89-94. PubMed ID: 116084 [TBL] [Abstract][Full Text] [Related]
5. Hyperlysinemia with saccharopinuria due to combined lysine-ketoglutarate reductase and saccharopine dehydrogenase deficiencies presenting as cystinuria. Cederbaum SD; Shaw KN; Dancis J; Hutzler J; Blaskovics JC J Pediatr; 1979 Aug; 95(2):234-8. PubMed ID: 571908 [TBL] [Abstract][Full Text] [Related]
11. The Metabolite Saccharopine Impairs Neuronal Development by Inhibiting the Neurotrophic Function of Glucose-6-Phosphate Isomerase. Guo Y; Wu J; Wang M; Wang X; Jian Y; Yang C; Guo W J Neurosci; 2022 Mar; 42(13):2631-2646. PubMed ID: 35135854 [TBL] [Abstract][Full Text] [Related]
12. [Saccharopinuria (a variant form of familial hyperlysinemia)]. Higashino K Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):191-4. PubMed ID: 9590025 [No Abstract] [Full Text] [Related]
13. [Inborn errors of lysine metabolism]. Divry P; Vianey-Liaud C; Mathieu M Ann Biol Clin (Paris); 1991; 49(1):27-35. PubMed ID: 1904694 [TBL] [Abstract][Full Text] [Related]
14. Further studies on hyperlysinemia associated with retardation. Ghadimi H; Zischka R; Binnington VI Am J Dis Child; 1967 Jan; 113(1):146-51. PubMed ID: 6015892 [No Abstract] [Full Text] [Related]
15. Identification of the alpha-aminoadipic semialdehyde synthase gene, which is defective in familial hyperlysinemia. Sacksteder KA; Biery BJ; Morrell JC; Goodman BK; Geisbrecht BV; Cox RP; Gould SJ; Geraghty MT Am J Hum Genet; 2000 Jun; 66(6):1736-43. PubMed ID: 10775527 [TBL] [Abstract][Full Text] [Related]
16. Clinical and biochemical studies on periodic hyperammonemia with hyperlysinemia and homocitrullinuria. Oyanagi K; Sogawa H; Sato S; Orii T; Nakao T Tohoku J Exp Med; 1976 Oct; 120(2):105-12. PubMed ID: 982431 [TBL] [Abstract][Full Text] [Related]