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Journal Abstract Search

273 related items for PubMed ID: 803128

  • 1. 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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  • 2. Prolidase deficiency with iminodipeptiduria: biochemical investigations and first results of attempted therapy.
    Charpentier C, Dagbovie K, Lemonnier A, Larregue M, Johnstone RA.
    J Inherit Metab Dis; 1981 Oct 18; 4(2):77-8. PubMed ID: 6790856
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  • 3. Studies on a patient with iminodipeptiduria. II. Lack of prolidase activity in blood cells.
    Umemura S.
    Physiol Chem Phys; 1978 Oct 18; 10(3):279-83. PubMed ID: 733941
    [No Abstract] [Full Text] [Related]

  • 4. Prolidase deficiency: a patient without hydroxyproline-containing iminodipeptides in urine.
    Wysocki SJ, Hahnel R, Mahoney T, Wilson RG, Panegyres PK.
    J Inherit Metab Dis; 1988 Oct 18; 11(2):161-5. PubMed ID: 3139928
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  • 5. The role of prolidase as an enzyme participating in the metabolism of collagen.
    Pałka JA.
    Rocz Akad Med Bialymst; 1996 Oct 18; 41(2):149-60. PubMed ID: 9020526
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  • 6. Further studies on a patient with iminodipeptiduria: a probable case of prolidase deficiency.
    Buist NR, Strandholm JJ, Bellinger JF, Kennaway NG.
    Metabolism; 1972 Dec 18; 21(12):1113-23. PubMed ID: 4674498
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  • 8. Liquid chromatography-mass spectrometry for the qualitative analyses of iminodipeptides in the urine of patients with prolidase deficiency.
    Kodama H, Nakamura H, Sugahara K, Numajiri Y.
    J Chromatogr; 1990 May 18; 527(2):279-88. PubMed ID: 2387877
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  • 9. Prolidase deficiency with imidodipeptiduria. A familial case with and without clinical symptoms.
    Isemura M, Hanyu T, Gejyo F, Nakazawa R, Igarashi R, Matsuo S, Ikeda K, Sato Y.
    Clin Chim Acta; 1979 May 02; 93(3):401-7. PubMed ID: 445856
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  • 10. Prolidase deficiency in cultured human fibroblasts: biochemical pathology and iminodipeptide-enhanced growth.
    Dolenga M, Hechtman P.
    Pediatr Res; 1992 Oct 02; 32(4):479-82. PubMed ID: 1437403
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  • 11. [Inborn errors of imino acid metabolism].
    Endo F.
    Nihon Rinsho; 1992 Jul 02; 50(7):1568-74. PubMed ID: 1404885
    [Abstract] [Full Text] [Related]

  • 12. Increased manganese content and reduced arginase activity in erythrocytes of a patient with prolidase deficiency (iminodipeptiduria).
    Lombeck I, Wendel U, Versieck J, van Ballenberghe L, Bremer HJ, Duran R, Wadman S.
    Eur J Pediatr; 1986 Apr 02; 144(6):571-3. PubMed ID: 3709569
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  • 13. Prolidase deficiency.
    Pedersen PS, Christensen E, Brandt NJ.
    Acta Paediatr Scand; 1983 Sep 02; 72(5):785-8. PubMed ID: 6637477
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  • 14. [Prolidase deficiency].
    Tanoue A, Endo F.
    Ryoikibetsu Shokogun Shirizu; 1998 Sep 02; (18 Pt 1):160-2. PubMed ID: 9590016
    [No Abstract] [Full Text] [Related]

  • 15. Measurement of iminodipeptides in the serum of patients with prolidase deficiency using liquid chromatography-mass spectrometry.
    Sugahara K, Jianying Z, Yamamoto Y, Yasuda K, Kodama H, Kodama H.
    Eur J Clin Chem Clin Biochem; 1994 Mar 02; 32(3):113-7. PubMed ID: 8031960
    [Abstract] [Full Text] [Related]

  • 16. Prolidase and prolidase deficiency.
    Myara I, Charpentier C, Lemonnier A.
    Life Sci; 1984 May 21; 34(21):1985-98. PubMed ID: 6727550
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  • 17. Clinical and biochemical characteristics of prolidase deficiency in siblings.
    Freij BJ, Levy HL, Dudin G, Mutasim D, Deeb M, Der Kaloustian VM.
    Am J Med Genet; 1984 Nov 21; 19(3):561-71. PubMed ID: 6507502
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  • 20. In situ activation of human erythrocyte prolidase: potential for enzyme replacement therapy in prolidase deficiency.
    Hechtman P, Richter A, Corman N, Leong YM.
    Pediatr Res; 1988 Dec 21; 24(6):709-12. PubMed ID: 3205627
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