These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
120 related articles for article (PubMed ID: 5599161)
21. [Inborn errors of amino acid metabolism--pathogenesis of mental retardation]. Tada K; Yoshida T Shinkei Kenkyu No Shimpo; 1968; 12(1):137-46. PubMed ID: 4881483 [No Abstract] [Full Text] [Related]
23. Spectrum of hypermethioninemia in neonatal screening. Chien YH; Chiang SC; Huang A; Hwu WL Early Hum Dev; 2005 Jun; 81(6):529-33. PubMed ID: 15935930 [TBL] [Abstract][Full Text] [Related]
24. 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]
25. [Cystathioninuria]. Broyer M; Berger R Presse Med (1893); 1969 Oct; 77(44):1562. PubMed ID: 5367624 [No Abstract] [Full Text] [Related]
27. [A case of homocystinuria missed by the newborn screening]. Watanabe T; Kuroda Y; Naito E; Ito M; Takeda E; Toshima K; Miyao M; Tomita T; Furukawa S No To Hattatsu; 1985 May; 17(3):265-8. PubMed ID: 4015895 [No Abstract] [Full Text] [Related]
29. Pathogenesis of mental retardation in amino acid disorders. Tada K Int J Neurol; 1976; 11(1):73-84. PubMed ID: 1017916 [No Abstract] [Full Text] [Related]
33. 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]
34. [Methionine malabsorption]. Hooft C; Timmermans J; Snoeck J; Antener I; Oyaert W; Van den Hende C Verh K Vlaam Acad Geneeskd Belg; 1966; 28(1):15-39. PubMed ID: 5911135 [No Abstract] [Full Text] [Related]
35. [Cerebral findings in aminoaciduria]. Martin JJ; Van Bogaert L; Guazzi GC Confin Neurol; 1968; 30(2):97-116. PubMed ID: 5698580 [No Abstract] [Full Text] [Related]
36. HOMOCYSTINURIA, AN ERROR IN THE METABOLISM OF METHIONINE. GERRITSEN T; WAISMAN HA Pediatrics; 1964 Mar; 33():413-20. PubMed ID: 14129086 [No Abstract] [Full Text] [Related]
37. HOMOCYSTINURIA: AN ENZYMATIC DEFECT. MUDD SH; FINKELSTEIN JD; IRREVERRE F; LASTER L Science; 1964 Mar; 143(3613):1443-5. PubMed ID: 14107447 [TBL] [Abstract][Full Text] [Related]
38. AMINOACIDURIA. EFRON ML N Engl J Med; 1965 May; 272():1107-13 CONCL. PubMed ID: 14281555 [No Abstract] [Full Text] [Related]
39. General anesthesia for patient with type III homocystinuria (tetrahydrofolate reductase deficiency). Yamada T; Hamada H; Mochizuki S; Sutoh M; Tsuji M; Kawamoto M; Yuge O J Clin Anesth; 2005 Nov; 17(7):565-7. PubMed ID: 16297760 [TBL] [Abstract][Full Text] [Related]
40. 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] [Previous] [Next] [New Search]