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Journal Abstract Search

136 related items for PubMed ID: 7239517

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. Measurement of prolidase activity in erythrocytes using isotachophoresis.
    Mikasa H, Arata J, Kodama H.
    J Chromatogr; 1984 Oct 12; 310(2):401-6. PubMed ID: 6511856
    [No Abstract] [Full Text] [Related]

  • 3. 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 12; 4(2):77-8. PubMed ID: 6790856
    [Abstract] [Full Text] [Related]

  • 4. Studies on a patient with iminodipeptiduria. II. Lack of prolidase activity in blood cells.
    Umemura S.
    Physiol Chem Phys; 1978 Oct 12; 10(3):279-83. PubMed ID: 733941
    [No Abstract] [Full Text] [Related]

  • 5. Human erythrocyte prolidase and prolidase deficiency.
    Endo F, Matsuda I, Ogata A, Tanaka S.
    Pediatr Res; 1982 Mar 12; 16(3):227-31. PubMed ID: 7063276
    [Abstract] [Full Text] [Related]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8. Substrate specificity of manganese-activated prolidase in control and prolidase-deficient cultured skin fibroblasts.
    Butterworth J, Priestman D.
    J Inherit Metab Dis; 1984 Oct 18; 7(1):32-4. PubMed ID: 6429439
    [Abstract] [Full Text] [Related]

  • 9. [Inborn errors of imino acid metabolism].
    Endo F.
    Nihon Rinsho; 1992 Jul 18; 50(7):1568-74. PubMed ID: 1404885
    [Abstract] [Full Text] [Related]

  • 10. Prolidase deficiency with hyperimmunoglobulin E: a case report.
    Lopes I, Marques L, Neves E, Silva A, Taveira M, Pena R, Vilarinho L, Martins E.
    Pediatr Allergy Immunol; 2002 Apr 18; 13(2):140-2. PubMed ID: 12000488
    [Abstract] [Full Text] [Related]

  • 11. Biochemical investigations on prolidase and prolinase in erythrocytes from patients with prolidase deficiency.
    Kodama H, Mikasa H, Ohhashi T, Ohno T, Arata J.
    Clin Chim Acta; 1988 Apr 29; 173(3):317-23. PubMed ID: 3383432
    [No Abstract] [Full Text] [Related]

  • 12. [Prolidase deficiency].
    Tanoue A, Endo F.
    Ryoikibetsu Shokogun Shirizu; 1998 Apr 29; (18 Pt 1):160-2. PubMed ID: 9590016
    [No Abstract] [Full Text] [Related]

  • 13. Studies on prolidase deficiency with a possible defect in collagen metabolism.
    Isemura M, Hanyu T, Ono T, Igarashi R, Sato Y, Gejyo F, Nakazawa R, Miyakawa T, Takagi T, Kuboki Y, Sasaki S.
    Tohoku J Exp Med; 1981 May 29; 134(1):21-8. PubMed ID: 7314091
    [Abstract] [Full Text] [Related]

  • 14. 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 29; 32(3):113-7. PubMed ID: 8031960
    [Abstract] [Full Text] [Related]

  • 15. Characterization of prolidase activity in erythrocytes from a patient with prolidase deficiency: comparison with prolidase I and II purified from normal human erythrocytes.
    Liu G, Nakayama K, Sagara Y, Awata S, Yamashita K, Manabe M, Kodama H.
    Clin Biochem; 2005 Jul 29; 38(7):625-31. PubMed ID: 16009141
    [Abstract] [Full Text] [Related]

  • 16. Prolidase deficiency among an Israeli population: prenatal diagnosis in a genetic disorder with uncertain prognosis.
    Mandel H, Abeling N, Gutman A, Berant M, Scholten EG, Sheiman C, Luder A, van Gennip AH.
    Prenat Diagn; 2000 Nov 29; 20(11):927-9. PubMed ID: 11113899
    [Abstract] [Full Text] [Related]

  • 17. Biochemical basis of prolidase deficiency. Polypeptide and RNA phenotypes and the relation to clinical phenotypes.
    Endo F, Tanoue A, Kitano A, Arata J, Danks DM, Lapière CM, Sei Y, Wadman SK, Matsuda I.
    J Clin Invest; 1990 Jan 29; 85(1):162-9. PubMed ID: 1688567
    [Abstract] [Full Text] [Related]

  • 18. Characteristics of prolidase from the erythrocytes of normal humans and patients with prolidase deficiency and their mother.
    Nakayama K, Awata S, Zhang J, Kaba H, Manabe M, Kodama H.
    Clin Chem Lab Med; 2003 Oct 29; 41(10):1323-8. PubMed ID: 14580160
    [Abstract] [Full Text] [Related]

  • 19. [Prolidase and manganese deficiency. Apropos of a case: diagnosis and treatment].
    Larrèque M, Charpentier C, Laidet B, Lambert M, Bressieux JM, Prigent F, Canuel C, Tanzer J.
    Ann Dermatol Venereol; 1982 Oct 29; 109(8):667-78. PubMed ID: 7187192
    [Abstract] [Full Text] [Related]

  • 20. Prolidase deficiency and systemic lupus erythematosus.
    Shrinath M, Walter JH, Haeney M, Couriel JM, Lewis MA, Herrick AL.
    Arch Dis Child; 1997 May 29; 76(5):441-4. PubMed ID: 9196362
    [Abstract] [Full Text] [Related]

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