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3. Familial hyperlysinemia: enzyme studies, diagnostic methods, comments on terminology. Dancis J; Hutzler J; Cox RP Am J Hum Genet; 1979 May; 31(3):290-9. PubMed ID: 463877 [TBL] [Abstract][Full Text] [Related]
4. Familial hyperlysinemias. Purification and characterization of the bifunctional aminoadipic semialdehyde synthase with lysine-ketoglutarate reductase and saccharopine dehydrogenase activities. Markovitz PJ; Chuang DT; Cox RP J Biol Chem; 1984 Oct; 259(19):11643-6. PubMed ID: 6434529 [TBL] [Abstract][Full Text] [Related]
5. Propionic acidemia and hyperlysinemia in a case with ornithine transcarbamylase (OTC) deficiency. Krieger I; Bachmann C; Gronemeyer WH; Cejka J J Clin Endocrinol Metab; 1976 Oct; 43(4):796-802. PubMed ID: 977722 [TBL] [Abstract][Full Text] [Related]
6. Enzyme studies in a patient with saccharopinuria: a defect of lysine metabolism. Fellows FC; Carson NA Pediatr Res; 1974 Jan; 8(1):42-9. PubMed ID: 4809305 [No Abstract] [Full Text] [Related]
8. 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]
9. 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]
11. Metabolism of lysine in alpha-aminoadipic semialdehyde dehydrogenase-deficient fibroblasts: evidence for an alternative pathway of pipecolic acid formation. Struys EA; Jakobs C FEBS Lett; 2010 Jan; 584(1):181-6. PubMed ID: 19932104 [TBL] [Abstract][Full Text] [Related]
12. Familial hyperlysinemias--multiple enzyme deficiencies associated with the bifunctional aminoadipic semialdehyde synthase. Cox RP; Markovitz PJ; Chuang DT Trans Am Clin Climatol Assoc; 1986; 97():69-81. PubMed ID: 3939388 [No Abstract] [Full Text] [Related]
13. The prognosis of hyperlysinemia: an interim report. Dancis J; Hutzler J; Ampola MG; Shih VE; van Gelderen HH; Kirby LT; Woody NC Am J Hum Genet; 1983 May; 35(3):438-42. PubMed ID: 6407303 [TBL] [Abstract][Full Text] [Related]
14. [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]
15. [Hyperlysinemia and lysine intolerance]. Oyanagi K Nihon Rinsho; 1978 May; Suppl():1358-9. PubMed ID: 691354 [No Abstract] [Full Text] [Related]
16. Intestinal absorption of L-arginine and L-lysine in familial protein intolerance. Kekomäki M Ann Paediatr Fenn; 1968; 14(1):18-22. PubMed ID: 5685037 [No Abstract] [Full Text] [Related]