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3. 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]
6. 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]
7. Homocystinuria: recent research into cause and treatment. Stevens V Nurs Times; 1968 Feb; 64(7):210-2. PubMed ID: 5636233 [No Abstract] [Full Text] [Related]
8. [Homocystinuria]. Broyer M; Berger R Presse Med (1893); 1968 Apr; 76(19):913-4. PubMed ID: 5645356 [No Abstract] [Full Text] [Related]
9. Ocular pathology in homocystinuria. Henkind P; Ashton N Trans Ophthalmol Soc U K (1962); 1965; 85():21-38. PubMed ID: 5227183 [No Abstract] [Full Text] [Related]
10. [Typical hyperaminoaciduria and disulfiduria associated with mental retardation in an incest-born child]. Hyánek J; Seemanova E; Hoza J Cesk Pediatr; 1970 Mar; 25(3):115-8. PubMed ID: 5445347 [No Abstract] [Full Text] [Related]
11. [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]
12. 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]
13. [Defects in the metabolism of methionine: methioninemia, homocystinurie, homoserinuria and cystinuria]. Gjessing LR Tidsskr Nor Laegeforen; 1967 Feb; 87(3):154-8. PubMed ID: 5599161 [No Abstract] [Full Text] [Related]
14. [Ocular changes in homocystinuria. II. The amino acids of the aqueous humor]. Martenet AC; Curtius HC; Anders PW Arch Ophtalmol Rev Gen Ophtalmol; 1968; 28(3):295-302. PubMed ID: 4233892 [No Abstract] [Full Text] [Related]
15. Creatine metabolism in combined methylmalonic aciduria and homocystinuria. Bodamer OA; Sahoo T; Beaudet AL; O'Brien WE; Bottiglieri T; Stöckler-Ipsiroglu S; Wagner C; Scaglia F Ann Neurol; 2005 Apr; 57(4):557-60. PubMed ID: 15786446 [TBL] [Abstract][Full Text] [Related]
16. [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]
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. Homocystinuria due to cystathionine synthase deficiency: the metabolism of L-methionine. Laster L; Mudd SH; Finkelstein JD; Irreverre F J Clin Invest; 1965 Oct; 44(10):1708-19. PubMed ID: 5840537 [No Abstract] [Full Text] [Related] [Next] [New Search]