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Journal Abstract Search

129 related items for PubMed ID: 3709569

  • 1. 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; 144(6):571-3. PubMed ID: 3709569
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  • 2. 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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  • 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 18; 4(2):77-8. PubMed ID: 6790856
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  • 4. 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 18; 24(6):709-12. PubMed ID: 3205627
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  • 6. Optimal conditions for prolidase assay by proline colorimetric determination: application to iminodipeptiduria.
    Myara I, Charpentier C, Lemonnier A.
    Clin Chim Acta; 1982 Oct 27; 125(2):193-205. PubMed ID: 7139961
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  • 8. In-vitro responses to ascorbate and manganese in fibroblasts from a patient with prolidase deficiency and iminodipeptiduria: cell growth, prolidase activity and collagen metabolism.
    Myara I, Charpentier C, Wolfrom C, Gautier M, Lemonnier A, Larregue M, Chamson A, Frey J.
    J Inherit Metab Dis; 1983 Oct 27; 6(1):27-31. PubMed ID: 6408304
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  • 9. [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 27; 109(8):667-78. PubMed ID: 7187192
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  • 12. Effects of amino acids and its metabolites on prolidase activity against various iminodipeptides in erythrocytes from normal human and a patient with prolidase deficiency.
    Liu G, Nakayama K, Awata S, Wang W, Yamashita K, Manabe M, Kodama H.
    Clin Chim Acta; 2004 Dec 27; 350(1-2):211-7. PubMed ID: 15530480
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  • 13. 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 27; 19(3):561-71. PubMed ID: 6507502
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  • 14. 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 Nov 27; 11(2):161-5. PubMed ID: 3139928
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  • 15. 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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  • 17. Further studies on a patient with iminodipeptiduria: a probable case of prolidase deficiency.
    Buist NR, Strandholm JJ, Bellinger JF, Kennaway NG.
    Metabolism; 1972 Dec 02; 21(12):1113-23. PubMed ID: 4674498
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  • 19. Characterization of prolidase I and II from erythrocytes of a control, a patient with prolidase deficiency and her mother.
    Ohhashi T, Ohno T, Arata J, Sugahara K, Kodama H.
    Clin Chim Acta; 1990 Jan 31; 187(1):1-9. PubMed ID: 2317925
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  • 20. Substrate specificity of manganese-activated prolidase in control and prolidase-deficient cultured skin fibroblasts.
    Butterworth J, Priestman D.
    J Inherit Metab Dis; 1984 Jan 31; 7(1):32-4. PubMed ID: 6429439
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