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Journal Abstract Search
182 related items for PubMed ID: 533224
1. Hydroxyproline metabolism in type II hyperprolinaemia. Similä S. Ann Clin Biochem; 1979 Jul; 16(4):177-81. PubMed ID: 533224 [Abstract] [Full Text] [Related]
2. 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]
3. N-(pyrrole-2-carboxyl) glycine a diagnostic marker of hyperprolinaemia type II: mass spectra of trimethylsilyl derivatives. Walker V, Mills GA. Clin Chim Acta; 2009 Jul; 405(1-2):153-4. PubMed ID: 19376100 [No Abstract] [Full Text] [Related]
4. Type II hyperprolinemia: a case report. Onenli-Mungan N, Yüksel B, Elkay M, Topaloğlu AK, Baykal T, Ozer G. Turk J Pediatr; 2004 Jul; 46(2):167-9. PubMed ID: 15214748 [Abstract] [Full Text] [Related]
5. [Hyperprolinemia and hydroxyprolinemia]. Berger R, Broyer M. Presse Med (1893); 1969 May 28; 77(26):957-8. PubMed ID: 5795142 [No Abstract] [Full Text] [Related]
8. Genetic evidence for a common enzyme catalyzing the second step in the degradation of proline and hydroxyproline. Valle D, Goodman SI, Harris SC, Phang JM. J Clin Invest; 1979 Nov 28; 64(5):1365-70. PubMed ID: 500817 [Abstract] [Full Text] [Related]
12. Low proline diet in type I hyperprolinaemia. Harries JT, Piesowicz AT, Seakins JW, Francis DE, Wolff OH. Arch Dis Child; 1971 Feb 28; 46(245):72-81. PubMed ID: 5555491 [Abstract] [Full Text] [Related]
13. Asymptomatic type II hyperprolinaemia associated with hyperglycinaemia in three sibs. Pavone L, Mollica F, Levy HL. Arch Dis Child; 1975 Aug 28; 50(8):637-41. PubMed ID: 1200680 [Abstract] [Full Text] [Related]
14. Iminoglycinuria in a child in Czechoslovakia. Blehová B, Păzoutová N, Hyánek J, Jirásek J. Humangenetik; 1973 Jul 20; 19(2):207-10. PubMed ID: 4744406 [No Abstract] [Full Text] [Related]
17. Iminoglycinuria: a benign type of inherited aminoaciduria. Coşkun T, Ozalp I, Tokatli A. Turk J Pediatr; 1993 Jul 20; 35(2):121-5. PubMed ID: 7504361 [Abstract] [Full Text] [Related]