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4. Hyperornithinemia, hyperammonemia, and homocitrullinuria. A new disorder of amino acid metabolism associated with myoclonic seizures and mental retardation. Shih VE; Efron ML; Moser HW Am J Dis Child; 1969 Jan; 117(1):83-92. PubMed ID: 5782534 [No Abstract] [Full Text] [Related]
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. The pathogenesis of mental retardation in phenylketonuria and other inborn errors of amino acid metabolism. Menkes JH Pediatrics; 1967 Feb; 39(2):297-308. PubMed ID: 5335144 [No Abstract] [Full Text] [Related]
7. [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]
8. [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]
9. 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]
11. 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]
12. 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]
13. Mental retardation in a family with phenylketonuria and mild hyperphenylalaninemia. Cohen BE; Szeinberg A; Berman W; Aviad Y; Crispin M; Hirshorn N; Goland R Pediatrics; 1969 Nov; 44(5):655-60. PubMed ID: 5374976 [No Abstract] [Full Text] [Related]
14. [The detection of aminoacidopathies causing mental retardation]. Thiriar M; Vis HL Acta Paediatr Belg; 1966; 20(5):333-70. PubMed ID: 5330633 [No Abstract] [Full Text] [Related]
15. Enzyme defect in saccharopinuria. Simell O; Johansson T; Aula P J Pediatr; 1973 Jan; 82(1):54-7. PubMed ID: 4404606 [No Abstract] [Full Text] [Related]
17. Mental retardation due to inborn errors of amino acid metabolism in Puerto Rico. Results of a screening test and a review of other documented cases. Crosby PF Bol Asoc Med P R; 1971 Jul; 63(7):184-6. PubMed ID: 5286510 [No Abstract] [Full Text] [Related]
18. [Study of urinary elimination of amino acids in infantile cerebral diseases]. Zoratto E; Cocuzza S; Lumare A Minerva Pediatr; 1965 Oct; 17(31):1646-51. PubMed ID: 5858644 [No Abstract] [Full Text] [Related]
19. Screening for aminoacid disorders in mental retardation. Jyothy A; Reddy PP Indian Pediatr; 1984 May; 21(5):381-8. PubMed ID: 6480090 [No Abstract] [Full Text] [Related]
20. Prevalence of homocystinuria among the mentally retarded: evaluation of a specific screening test. Spaeth GL; Barber GW Pediatrics; 1967 Oct; 40(4):586-9. PubMed ID: 6051058 [No Abstract] [Full Text] [Related] [Next] [New Search]