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PUBMED FOR HANDHELDS

Journal Abstract Search

98 related items for PubMed ID: 5434118

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  • 6. Hydroxyprolinemia and increased excretion of free hydroxyproline in early infancy.
    Morrow G, Kivitikko KI, Prockop DJ.
    J Clin Endocrinol Metab; 1966 Sep; 26(9):1012-4. PubMed ID: 5926946
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  • 7. Hydroxyprolinemia: a case report.
    Rama Rao BS, Subhash MN, Narayanan HS.
    Indian Pediatr; 1974 Dec; 11(12):829-30. PubMed ID: 4448548
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  • 10. 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
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  • 11. Catabolism and excretion of free hydroxyproline in infancy.
    Morrow G, Kivirikko KI, Prockop DJ.
    J Clin Endocrinol Metab; 1967 Oct; 27(10):1365-71. PubMed ID: 6050957
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  • 12. Hydroxyprolinemia.
    Swarna M, Rao DN, Kumari CK, Reddy PP.
    Indian J Pediatr; 1989 Oct; 56(4):527-8. PubMed ID: 2633993
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  • 13. 3-Hydroxyproline content of normal urine.
    Adams E, Ramaswamy S, Lamon M.
    J Clin Invest; 1978 Jun; 61(6):1482-7. PubMed ID: 659611
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  • 15. Iminodipeptiduria: a genetic defect in recycling collagen; a method for determining prolidase in erythrocytes.
    Jackson SH, Dennis AW, Greenberg M.
    Can Med Assoc J; 1975 Oct 18; 113(8):759, 762-3. PubMed ID: 803128
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  • 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 18; 31(2):173-82. PubMed ID: 955941
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  • 18. Familial iminoglycinuria. An inborn error of renal tubular transport.
    Rosenberg LE, Durant JL, Elsas LJ.
    N Engl J Med; 1968 Jun 27; 278(26):1407-13. PubMed ID: 5652624
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  • 19. 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 27; 63(7):184-6. PubMed ID: 5286510
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  • 20. Pathogenesis of mental retardation in amino acid disorders.
    Tada K.
    Int J Neurol; 1976 Jul 27; 11(1):73-84. PubMed ID: 1017916
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