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5. [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]
6. Clinical, biochemical, molecular and therapeutic aspects of 2 new cases of 2-aminoadipic semialdehyde synthase deficiency. Tondo M; Calpena E; Arriola G; Sanz P; Martorell L; Ormazabal A; Castejon E; Palacin M; Ugarte M; Espinos C; Perez B; Perez-Dueñas B; Pérez-Cerda C; Artuch R Mol Genet Metab; 2013 Nov; 110(3):231-6. PubMed ID: 23890588 [TBL] [Abstract][Full Text] [Related]
7. [Hyperlysinemia and lysine intolerance]. Oyanagi K Nihon Rinsho; 1978 May; Suppl():1358-9. PubMed ID: 691354 [No Abstract] [Full Text] [Related]
8. 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]
9. Hyperlysinemia associated with retardation. Ghadimi H; Binnington VI; Pecora P N Engl J Med; 1965 Sep; 273(14):723-9. PubMed ID: 5825685 [No Abstract] [Full Text] [Related]
10. 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]