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22. [Recent developments in amino-acidopathies]. Farriaux JP Lille Med; 1971 Feb; 16(2):342-55. PubMed ID: 5575812 [No Abstract] [Full Text] [Related]
23. The role of homocystinuria in the etiopathogenesis of children's mental deficiency. Gebala A; Kozlowska T Acta Univ Carol Med Monogr; 1973; 56():179-82. PubMed ID: 4791769 [No Abstract] [Full Text] [Related]
24. [Biochemistry of mental retardation]. Yoshida M; Seyama Y; Yamakwa T Nihon Rinsho; 1976 Sep; 34(9):2726-34. PubMed ID: 825670 [No Abstract] [Full Text] [Related]
25. Lipid composition of brain in a patient with mental retardation due to encephalopathy in an infantile period and one due to homocystinuria. Saito S; Tamai Y; Matsushita M Jpn J Exp Med; 1979 Aug; 49(4):257-64. PubMed ID: 502082 [TBL] [Abstract][Full Text] [Related]
26. [Homocystinuria (apropos of a case)]. Gaudier B; François P; Biserte G; Nuyts JP; Bombart E Pediatrie; 1966 Dec; 21(8):889-98. PubMed ID: 5985819 [No Abstract] [Full Text] [Related]
27. 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]
34. [Changes in metabolism of tryptophan of a familial type with mental deficiency]. Giovannini M; Careddu P Pediatria (Napoli); 1967; 75(1):48-59. PubMed ID: 5601245 [No Abstract] [Full Text] [Related]
35. [Ocular and systemic complications of homocystinuria: a report of five cases]. Rais L; Wafi M; Lahbil D; Iraki M; Fekkak J; Hamdani M; Benchekroun W; Rachid R; Belhadji M; Laouissi N; Zaghloul K; Amraoui A J Fr Ophtalmol; 2003 Dec; 26(10):1045-50. PubMed ID: 14691398 [TBL] [Abstract][Full Text] [Related]
36. [Attempted clinical orientation in the diagnosis of amino acid metabolism disorders. I. Urinary symptoms, neuropsychic symptoms and ocular symtpoms]. Boisse J Presse Med (1893); 1968 Apr; 76(19):903-6. PubMed ID: 5645352 [No Abstract] [Full Text] [Related]
37. Attempts at use of strychnine sulfate in the treatment of nonketotic hyperglycinemia. MacDermot KD; Nelson W; Reichert CM; Schulman JD Pediatrics; 1980 Jan; 65(1):61-4. PubMed ID: 7355037 [TBL] [Abstract][Full Text] [Related]
38. A new type of idiopathic hyperglycinemia with hypo-oxaluria. Gerritsen T; Kaveggia E; Waisman HA Pediatrics; 1965 Dec; 36(6):882-91. PubMed ID: 5846830 [No Abstract] [Full Text] [Related]
39. [Disorders of amino acid metabolism associated with mental retardation]. Humbel R Rev Neuropsychiatr Infant; 1966 Jun; 14(6):429-58. PubMed ID: 5329178 [No Abstract] [Full Text] [Related]
40. Hydroxyprolinemia as an illustration of nonessential enzymes in man. Prockop DJ N Engl J Med; 1970 Aug; 283(9):487. PubMed ID: 5434118 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]