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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

331 related items for PubMed ID: 14709855

  • 1. A case of a novel mutant vasopressin receptor-dependent nephrogenic diabetes insipidus with bilateral non-obstructive hydronephrosis in a middle aged man: differentiation from aquaporin-dependent nephrogenic diabetes insipidus by response of factor VII and von Willebrand factor to 1-diamino-8-arginine vasopressin administration.
    Miyakoshi M, Kamoi K, Uchida S, Sasaki S.
    Endocr J; 2003 Dec; 50(6):809-14. PubMed ID: 14709855
    [Abstract] [Full Text] [Related]

  • 2. Congenital nephrogenic diabetes insipidus presented with bilateral hydronephrosis: genetic analysis of V2R gene mutations.
    Yoo TH, Ryu DR, Song YS, Lee SC, Kim HJ, Kim JS, Choi HY, Kang SW.
    Yonsei Med J; 2006 Feb 28; 47(1):126-30. PubMed ID: 16502494
    [Abstract] [Full Text] [Related]

  • 3. Autosomal recessive nephrogenic diabetes insipidus caused by an aquaporin-2 mutation.
    Hochberg Z, Van Lieburg A, Even L, Brenner B, Lanir N, Van Oost BA, Knoers NV.
    J Clin Endocrinol Metab; 1997 Feb 28; 82(2):686-9. PubMed ID: 9024277
    [Abstract] [Full Text] [Related]

  • 4. Lack of responsiveness to 1-desamino-D arginin vasopressin (desmopressin) in male patients with nephrogenic syndrome of inappropriate antidiuresis: from bench to bedside.
    Vandergheynst F, Pradier O, Beukinga I, Kornreich A, Vassart G, Decaux G.
    Eur J Clin Invest; 2012 Mar 28; 42(3):254-9. PubMed ID: 21834801
    [Abstract] [Full Text] [Related]

  • 5. Normal response of factor VIII and von Willebrand factor to 1-deamino-8D-arginine vasopressin in nephrogenic diabetes insipidus.
    Brenner B, Seligsohn U, Hochberg Z.
    J Clin Endocrinol Metab; 1988 Jul 28; 67(1):191-3. PubMed ID: 3132483
    [Abstract] [Full Text] [Related]

  • 6. A novel AVPR2 gene mutation in a Chinese pedigree with nephrogenic diabetes insipidus.
    Zhao Y, Li K, Chen C, Lv X, Wang Y, Ma L, Fu S, Liu J.
    Postgrad Med; 2024 Aug 28; 136(6):683-690. PubMed ID: 39041787
    [Abstract] [Full Text] [Related]

  • 7. Normal fibrinolytic responses to 1-desamino-8-D-arginine vasopressin in patients with nephrogenic diabetes insipidus caused by mutations in the aquaporin 2 gene.
    van Lieburg AF, Knoers VV, Mallmann R, Proesmans W, van den Heuvel LP, Monnens LA.
    Nephron; 1996 Aug 28; 72(4):544-6. PubMed ID: 8730418
    [Abstract] [Full Text] [Related]

  • 8. V2R mutations and nephrogenic diabetes insipidus.
    Bichet DG.
    Prog Mol Biol Transl Sci; 2009 Aug 28; 89():15-29. PubMed ID: 20374732
    [Abstract] [Full Text] [Related]

  • 9. 1-Desamino-8-D-arginine vasopressin (DDAVP) in patients with congenital nephrogenic diabetes insipidus.
    Brink HS, Derkx FH, Boomsma F, Brommer EJ, Schalekamp MA.
    Neth J Med; 1993 Aug 28; 43(1-2):5-12. PubMed ID: 8232694
    [Abstract] [Full Text] [Related]

  • 10. Identification and characterization of a novel X-linked AVPR2 mutation causing partial nephrogenic diabetes insipidus: a case report and review of the literature.
    Neocleous V, Skordis N, Shammas C, Efstathiou E, Mastroyiannopoulos NP, Phylactou LA.
    Metabolism; 2012 Jul 28; 61(7):922-30. PubMed ID: 22386940
    [Abstract] [Full Text] [Related]

  • 11. Genetic forms of nephrogenic diabetes insipidus (NDI): Vasopressin receptor defect (X-linked) and aquaporin defect (autosomal recessive and dominant).
    Bichet DG, Bockenhauer D.
    Best Pract Res Clin Endocrinol Metab; 2016 Mar 28; 30(2):263-76. PubMed ID: 27156763
    [Abstract] [Full Text] [Related]

  • 12. [From genes to disease: from vasopressin-V2-receptor and aquaporine-2 to nephrogenic diabetes insipidus].
    Knoers NV, Deen PM.
    Ned Tijdschr Geneeskd; 2000 Dec 09; 144(50):2402-4. PubMed ID: 11145096
    [Abstract] [Full Text] [Related]

  • 13. Genetic deletion of the nuclear factor of activated T cells 5 in collecting duct principal cells causes nephrogenic diabetes insipidus.
    Petrillo F, Chernyakov D, Esteva-Font C, Poulsen SB, Edemir B, Fenton RA.
    FASEB J; 2022 Nov 09; 36(11):e22583. PubMed ID: 36197017
    [Abstract] [Full Text] [Related]

  • 14. Hemodynamic and coagulation responses to 1-desamino[8-D-arginine] vasopressin in patients with congenital nephrogenic diabetes insipidus.
    Bichet DG, Razi M, Lonergan M, Arthus MF, Papukna V, Kortas C, Barjon JN.
    N Engl J Med; 1988 Apr 07; 318(14):881-7. PubMed ID: 2965301
    [Abstract] [Full Text] [Related]

  • 15. Mutations in the vasopressin V2 receptor and aquaporin-2 genes in 12 families with congenital nephrogenic diabetes insipidus.
    Vargas-Poussou R, Forestier L, Dautzenberg MD, Niaudet P, Déchaux M, Antignac C.
    J Am Soc Nephrol; 1997 Dec 07; 8(12):1855-62. PubMed ID: 9402087
    [Abstract] [Full Text] [Related]

  • 16. The property of a novel v2 receptor mutant in a patient with nephrogenic diabetes insipidus.
    Inaba S, Hatakeyama H, Taniguchi N, Miyamori I.
    J Clin Endocrinol Metab; 2001 Jan 07; 86(1):381-5. PubMed ID: 11232028
    [Abstract] [Full Text] [Related]

  • 17. Identification and characterization of aquaporin-2 water channel mutations causing nephrogenic diabetes insipidus with partial vasopressin response.
    Canfield MC, Tamarappoo BK, Moses AM, Verkman AS, Holtzman EJ.
    Hum Mol Genet; 1997 Oct 07; 6(11):1865-71. PubMed ID: 9302264
    [Abstract] [Full Text] [Related]

  • 18. Characterization of an aquaporin-2 water channel gene mutation causing partial nephrogenic diabetes insipidus in a Mexican family: evidence of increased frequency of the mutation in the town of origin.
    Boccalandro C, De Mattia F, Guo DC, Xue L, Orlander P, King TM, Gupta P, Deen PM, Lavis VR, Milewicz DM.
    J Am Soc Nephrol; 2004 May 07; 15(5):1223-31. PubMed ID: 15100362
    [Abstract] [Full Text] [Related]

  • 19. A novel mutation affecting the arginine-137 residue of AVPR2 in dizygous twins leads to nephrogenic diabetes insipidus and attenuated urine exosome aquaporin-2.
    Hinrichs GR, Hansen LH, Nielsen MR, Fagerberg C, Dieperink H, Rittig S, Jensen BL.
    Physiol Rep; 2016 Apr 07; 4(8):. PubMed ID: 27117808
    [Abstract] [Full Text] [Related]

  • 20. A novel AVPR2 gene mutation of X-linked congenital nephrogenic diabetes insipidus in an Asian pedigree.
    Guo WH, Li Q, Wei HY, Lu HY, Qu HQ, Zhu M.
    J Int Med Res; 2016 Oct 07; 44(5):1131-1137. PubMed ID: 27565746
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 17.