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Journal Abstract Search
146 related items for PubMed ID: 1200680
21. Defective hydroxyproline metabolism in type II hyperprolinemia. Goodman SI, Mace JW, Miles BS, Teng CC, Brown SB. Biochem Med; 1974 Aug; 10(4):329-36. PubMed ID: 4851275 [No Abstract] [Full Text] [Related]
22. Acute encephalopathy associated with influenza virus infection in a patient with hyperprolinaemia type II. Kato Y, Ihara K, Miyako K, Kuhara T, Inoue Y, Hara T. J Inherit Metab Dis; 2005 Aug; 28(5):789-90. PubMed ID: 16151911 [Abstract] [Full Text] [Related]
23. The severe form of type I hyperprolinaemia results from homozygous inactivation of the PRODH gene. Jacquet H, Berthelot J, Bonnemains C, Simard G, Saugier-Veber P, Raux G, Campion D, Bonneau D, Frebourg T. J Med Genet; 2003 Jan; 40(1):e7. PubMed ID: 12525555 [No Abstract] [Full Text] [Related]
24. Pulmonary hypertension associated with nonketotic hyperglycinaemia. Cataltepe S, van Marter LJ, Kozakewich H, Wessel DL, Lee PJ, Levy HL. J Inherit Metab Dis; 2000 Mar; 23(2):137-44. PubMed ID: 10801055 [Abstract] [Full Text] [Related]
25. Hyperprolinemia. I. Study of a large family. Potter JL, Waickman FJ. J Pediatr; 1973 Oct; 83(4):635-8. PubMed ID: 4729989 [No Abstract] [Full Text] [Related]
29. Nonketotic hyperglycinaemia. Clinical findings and amino acid analyses on the plasma of a new case. Ferdinand W, Gordon RR, Owen G. Clin Chim Acta; 1970 Dec; 30(3):745-9. PubMed ID: 5493897 [No Abstract] [Full Text] [Related]
30. High urinary excretion of N-(pyrrole-2-carboxyl) glycine in type II hyperprolinemia. Wajner M, Wannmacher CM, Purkiss P. Clin Genet; 1990 Jun; 37(6):485-9. PubMed ID: 2383933 [Abstract] [Full Text] [Related]
31. Juvenile non-ketotic hyperglycinaemia in three siblings. Cole DE, Meek DC. J Inherit Metab Dis; 1985 Jun; 8 Suppl 2():123-4. PubMed ID: 3930859 [No Abstract] [Full Text] [Related]