These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

125 related articles for article (PubMed ID: 8876444)

  • 21. Iminopeptiduria, skin ulcerations, and edema in a boy with prolidase deficiency.
    Sheffield LJ; Schlesinger P; Faull K; Halpern BJ; Schier GM; Cotton RG; Hammond J; Danks DM
    J Pediatr; 1977 Oct; 91(4):578-83. PubMed ID: 908977
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Prolidase deficiency: biochemical study of erythrocyte and skin fibroblast prolidase activity in Italian patients.
    Zanaboni G; Dyne KM; Rossi A; Monafo V; Cetta G
    Haematologica; 1994; 79(1):13-8. PubMed ID: 15378943
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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; 13(2):140-2. PubMed ID: 12000488
    [TBL] [Abstract][Full Text] [Related]  

  • 24. The role of emerging techniques in the investigation of prolidase deficiency: from diagnosis to the development of a possible therapeutical approach.
    Viglio S; Annovazzi L; Conti B; Genta I; Perugini P; Zanone C; Casado B; Cetta G; Iadarola P
    J Chromatogr B Analyt Technol Biomed Life Sci; 2006 Feb; 832(1):1-8. PubMed ID: 16434239
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Prolidase deficiency. A metabolic disorder presenting with dermatologic signs.
    Freij BJ; Der Kaloustian VM
    Int J Dermatol; 1986 Sep; 25(7):431-3. PubMed ID: 3771038
    [No Abstract]   [Full Text] [Related]  

  • 26. Capillary electrophoresis for diagnosis of metabolic disease.
    Presto Elgstoen KB; Jellum E
    Electrophoresis; 1997 Sep; 18(10):1857-60. PubMed ID: 9372280
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [A case of prolidase deficiency with leg ulcers, hypoparathyroidism and imidodipeptiduria (author's transl)].
    Gejyo F; Nakazawa R; Ito G; Kinoshita Y; Ikarashi R; Isemura M
    Nihon Naika Gakkai Zasshi; 1980 Jan; 69(1):59-65. PubMed ID: 7373105
    [No Abstract]   [Full Text] [Related]  

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

  • 29. 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; 4(2):77-8. PubMed ID: 6790856
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [An inherent prolidase deficiency (author's transl)].
    Kodama H; Umemura S; Mizuhara S
    Tanpakushitsu Kakusan Koso; 1980; 25(6):590-6. PubMed ID: 7208949
    [No Abstract]   [Full Text] [Related]  

  • 31. Prolidase deficiency.
    Pedersen PS; Christensen E; Brandt NJ
    Acta Paediatr Scand; 1983 Sep; 72(5):785-8. PubMed ID: 6637477
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Hereditary prolidase deficiency. Contribution to differential therapy refractory leg ulcer diagnosis].
    Kasten R; Steinmann B; Voigtländer V
    Hautarzt; 2000 Nov; 51(11):846-51. PubMed ID: 11116849
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Capillary electrophoresis for clinical problem solving: analysis of urinary diagnostic metabolites and serum proteins.
    Jellum E; Dollekamp H; Blessum C
    J Chromatogr B Biomed Appl; 1996 Aug; 683(1):55-65. PubMed ID: 8876439
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Prolidase and prolidase deficiency.
    Myara I; Charpentier C; Lemonnier A
    Life Sci; 1984 May; 34(21):1985-98. PubMed ID: 6727550
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Optimal conditions for prolidase assay by proline colorimetric determination: application to iminodipeptiduria.
    Myara I; Charpentier C; Lemonnier A
    Clin Chim Acta; 1982 Oct; 125(2):193-205. PubMed ID: 7139961
    [TBL] [Abstract][Full Text] [Related]  

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

  • 37. Mutation analysis of five new patients affected by prolidase deficiency: the lack of enzyme activity causes necrosis-like cell death in cultured fibroblasts.
    Forlino A; Lupi A; Vaghi P; Icaro Cornaglia A; Calligaro A; Campari E; Cetta G
    Hum Genet; 2002 Oct; 111(4-5):314-22. PubMed ID: 12384772
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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; 85(1):162-9. PubMed ID: 1688567
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Kinetic study of prolidase activity in erythrocytes against different substrates using capillary electrophoresis with electrochemiluminescence detection.
    Zhou L; Yuan J; Yin J; Wang E
    J Chromatogr A; 2008 Jul; 1200(2):255-9. PubMed ID: 18550075
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Prolidase deficiency in cultured human fibroblasts: biochemical pathology and iminodipeptide-enhanced growth.
    Dolenga M; Hechtman P
    Pediatr Res; 1992 Oct; 32(4):479-82. PubMed ID: 1437403
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.