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145 related items for PubMed ID: 11113899

  • 1. 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; 20(11):927-9. PubMed ID: 11113899
    [Abstract] [Full Text] [Related]

  • 2. Consanguinity among the Arab and Jewish populations in Israel.
    Jaber L, Halpern GJ.
    Pediatr Endocrinol Rev; 2006 Aug; 3 Suppl 3():437-46. PubMed ID: 17551463
    [Abstract] [Full Text] [Related]

  • 3. Amelioration of prolidase deficiency in fibroblasts using adenovirus mediated gene transfer.
    Ikeda K, Tohyama J, Tsujino S, Sato K, Oono T, Arata J, Endo F, Sakuragawa N.
    Jpn J Hum Genet; 1997 Sep; 42(3):401-8. PubMed ID: 12503186
    [Abstract] [Full Text] [Related]

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

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

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

  • 7. Prenatal testing for genetic disorders among Arabs.
    Zlotogora J, Reshef N.
    Prenat Diagn; 1998 Mar 21; 18(3):219-24. PubMed ID: 9556038
    [Abstract] [Full Text] [Related]

  • 8. 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 21; 13(2):140-2. PubMed ID: 12000488
    [Abstract] [Full Text] [Related]

  • 9. Studies on a patient with iminodipeptiduria. II. Lack of prolidase activity in blood cells.
    Umemura S.
    Physiol Chem Phys; 1978 Apr 21; 10(3):279-83. PubMed ID: 733941
    [No Abstract] [Full Text] [Related]

  • 10. Glutaric aciduria type II, an unusual cause of prenatal polycystic kidneys: report of prenatal diagnosis and confirmation of autosomal recessive inheritance.
    Hockey A, Knowles S, Davies D, Carey W, Hurst J, Goldblatt J.
    Birth Defects Orig Artic Ser; 1993 Apr 21; 29(1):373-82. PubMed ID: 8280889
    [No Abstract] [Full Text] [Related]

  • 11. [Inborn errors of imino acid metabolism].
    Endo F.
    Nihon Rinsho; 1992 Jul 21; 50(7):1568-74. PubMed ID: 1404885
    [Abstract] [Full Text] [Related]

  • 12. 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 21; 85(1):162-9. PubMed ID: 1688567
    [Abstract] [Full Text] [Related]

  • 13. 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 17; 832(1):1-8. PubMed ID: 16434239
    [Abstract] [Full Text] [Related]

  • 14. Congenital expression of prolidase defect in prolidase deficiency.
    Naughten ER, Proctor SP, Levy HL, Coulombe JT, Ampola MG.
    Pediatr Res; 1984 Mar 17; 18(3):259-61. PubMed ID: 6728559
    [Abstract] [Full Text] [Related]

  • 15. Screening method for prolidase deficiency.
    Endo F, Matsuda I.
    Hum Genet; 1981 Mar 17; 56(3):349-51. PubMed ID: 7239517
    [No Abstract] [Full Text] [Related]

  • 16. 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]

  • 17. The impact of congenital malformations and Mendelian diseases on infant mortality in Israel.
    Zlotogora J, Leventhal A, Amitai Y.
    Isr Med Assoc J; 2003 Jun 02; 5(6):416-8. PubMed ID: 12841013
    [Abstract] [Full Text] [Related]

  • 18. Prenatal genetic diagnosis (second of three parts).
    Milunsky A, Littlefield JW, Kanfer JN, Kolodny EH, Shih VE, Atkins L.
    N Engl J Med; 1970 Dec 24; 283(26):1441-7. PubMed ID: 4098222
    [No Abstract] [Full Text] [Related]

  • 19. Use of amniotic fluid amino acids in prenatal testing for argininosuccinic aciduria and citrullinaemia.
    Mandell R, Packman S, Laframboise R, Golbus MS, Schmidt K, Workman L, Saudubray JM, Shih VE.
    Prenat Diagn; 1996 May 24; 16(5):419-24. PubMed ID: 8843999
    [Abstract] [Full Text] [Related]

  • 20. Citrullinemia, report of a case, with studies on antenatal diagnosis.
    Roerdink FH, Gouw WL, Okken A, van der Blij JF, Luit-de Haan G, Hommes FA, Huisjes HJ.
    Pediatr Res; 1973 Nov 24; 7(11):863-9. PubMed ID: 4749002
    [No Abstract] [Full Text] [Related]

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