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Journal Abstract Search
101 related items for PubMed ID: 9063421
1. Hydroxyprolinemia: comparison of a patient and her unaffected twin sister. Kim SZ, Varvogli L, Waisbren SE, Levy HL. J Pediatr; 1997 Mar; 130(3):437-41. PubMed ID: 9063421 [Abstract] [Full Text] [Related]
2. Genetic cause and prevalence of hydroxyprolinemia. Staufner C, Haack TB, Feyh P, Gramer G, Raga DE, Terrile C, Sauer S, Okun JG, Fang-Hoffmann J, Mayatepek E, Prokisch H, Hoffmann GF, Kölker S. J Inherit Metab Dis; 2016 Sep; 39(5):625-632. PubMed ID: 27139199 [Abstract] [Full Text] [Related]
8. Hydroxyprolinemia as an illustration of nonessential enzymes in man. Prockop DJ. N Engl J Med; 1970 Aug 27; 283(9):487. PubMed ID: 5434118 [No Abstract] [Full Text] [Related]
9. [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]
17. Familial iminoglycinuria with normal intestinal absorption of glycine and imino acids in association with profound mental retardation, a possible "cerebral phenotype". Statter M, Ben-Zvi A, Shina A, Schein R, Russell A. Helv Paediatr Acta; 1976 Aug 28; 31(2):173-82. PubMed ID: 955941 [Abstract] [Full Text] [Related]
18. A syndrome of congenital ichthyosis, mental retardation, myopathy and anemia in dizygotic twin sisters. Karaca B. Ann Saudi Med; 2012 Aug 28; 32(5):547-8. PubMed ID: 22871629 [No Abstract] [Full Text] [Related]
19. Treatment of hydroxyprolinemia and hyperprolinemia. Efron ML. Am J Dis Child; 1967 Jan 28; 113(1):166-9. PubMed ID: 6015897 [No Abstract] [Full Text] [Related]
20. Cognitive functioning in two sisters with carbamyl phosphate synthetase I deficiency. Sassaman EA, Zartler AS, Mulick JA. J Pediatr Psychol; 1981 Jun 28; 6(2):171-5. PubMed ID: 7252721 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]