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.
2. Treatment of homocystinuria with a low-methionine diet, supplemental cystine, and a methyl donor. Perry TL; Hansen S; Love DL; Crawford LE; Tischler B Lancet; 1968 Aug; 2(7566):474-8. PubMed ID: 4175242 [No Abstract] [Full Text] [Related]
4. 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]
6. Some theoretical considerations in the treatment of homocystinuria. Waisman HA Am J Dis Child; 1967 Jan; 113(1):101-2. PubMed ID: 6015886 [No Abstract] [Full Text] [Related]
7. Nonketotic hyperglycinemia: an in vitro study of the glycine-serine conversion in liver of three patients and the effect of dietary methionine. De Groot CJ; Troelstra JA; Hommes FA Pediatr Res; 1970 May; 4(3):238-43. PubMed ID: 5423161 [No Abstract] [Full Text] [Related]
8. [Dietetics in hereditary enzyme deficiencies]. Royer P Sem Hop; 1970 Feb; 46(10):653-9. PubMed ID: 4314674 [No Abstract] [Full Text] [Related]
9. The biosynthesis of cystathionine in patients with homocystinuria. Wong PW; Komrower GM; Schwarz V Pediatr Res; 1968 May; 2(3):149-60. PubMed ID: 5659087 [No Abstract] [Full Text] [Related]
10. Dietary treatment of inborn errors of amino acid and carbohydrate metabolism. Bickel H; Schmidt H; Schürrle L Bibl Nutr Dieta; 1973; (18):181-201. PubMed ID: 4566397 [No Abstract] [Full Text] [Related]
11. [Role of nutrition in treating hereditary disorders of amino acid metabolism in children]. Barashnev IuI Vopr Pitan; 1973; 32(4):18-24. PubMed ID: 4781562 [No Abstract] [Full Text] [Related]
12. Recent advances in the early detection and treatment of inborn errors with brain damage. Bickel H Neuropadiatrie; 1969; 1(1):1-11. PubMed ID: 4942066 [No Abstract] [Full Text] [Related]
13. Population screening. Stabler SP; Mudd SH N Engl J Med; 2003 Apr; 348(16):1604-5; author reply 1604-5. PubMed ID: 12700387 [No Abstract] [Full Text] [Related]
14. [Dietetics of amino acid metabolism disorders]. Brissaud HE Sem Hop; 1971 Feb; 47(7):462-5. PubMed ID: 4323080 [No Abstract] [Full Text] [Related]
17. Pyridoxine treatment in homocystinuria. Turner B Lancet; 1967 Nov; 2(7526):1151. PubMed ID: 4168582 [No Abstract] [Full Text] [Related]
18. Plasma amino acid disturbance in infancy. I: Hypermethioninaemia and transient tyrosinaemia. Komrower GM; Robins AJ Arch Dis Child; 1969 Jun; 44(235):418-21. PubMed ID: 5785193 [No Abstract] [Full Text] [Related]
19. 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]