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2. 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]
4. 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]
5. Incidence of phenylketonuria and other inborn errors of the amino acid metabolism in the normal and mentally retarded population. Hyánek J; Homolka J; Seemanová E Rev Czech Med; 1974; 20(1):18-22. PubMed ID: 4815837 [No Abstract] [Full Text] [Related]
7. [A clinico-genealogic analysis of mentally retarded patients with abnormal amino acid metabolism]. Krasnopol'skaia KD; Marincheva GS; Stonova NS Zh Nevropatol Psikhiatr Im S S Korsakova; 1975; 75(10):1539-43. PubMed ID: 1210933 [No Abstract] [Full Text] [Related]
8. Ocular manifestations of familial hyperlysinemia. Smith TH; Holland MG; Woody NC Trans Am Acad Ophthalmol Otolaryngol; 1971; 75(2):355-60. PubMed ID: 5557172 [No Abstract] [Full Text] [Related]
9. [Disturbance of the Histidine Reabsorption of the Renal Tubes in Patient with Cystine Lysinuria in Conjunction with Severe Cerebral Damage (author's transl)]. Ludescher E; jarosch E; berger H Padiatr Padol; 1975; 10(1):66-73. PubMed ID: 1124211 [TBL] [Abstract][Full Text] [Related]
11. [Combined cystinuria-lysinuria in 2 brothers with mental retardation and morphologic and neurologic anomalies]. Thiriar MJ; Szliwowski HB; Vis HL Acta Neurol Psychiatr Belg; 1968 Mar; 68(3):216-27. PubMed ID: 4972603 [No Abstract] [Full Text] [Related]
12. 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]
13. [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]
14. 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]
15. Histidinemia. A case with resolution of myoclonic seizures after treatment with a low-histidine diet. Dyme IZ; Horwitz SJ; Bacchus B; Kerr DS Am J Dis Child; 1983 Mar; 137(3):256-8. PubMed ID: 6823923 [TBL] [Abstract][Full Text] [Related]
16. [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]
18. [Feeble mindedness caused by genetic disorders of amino acid metabolism]. Menne F Hippokrates; 1968 May; 39(10):357-67. PubMed ID: 4886426 [No Abstract] [Full Text] [Related]
19. Homocystinuria. Trial treatment of a 5-year old severely retarded child with a natural diet low in methionine. Carson NA Am J Dis Child; 1967 Jan; 113(1):95-7. PubMed ID: 6015915 [No Abstract] [Full Text] [Related]