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Journal Abstract Search

723 related items for PubMed ID: 29125546

  • 1. Hereditary Nephrogenic Diabetes Insipidus: Pathophysiology and Possible Treatment. An Update.
    Milano S, Carmosino M, Gerbino A, Svelto M, Procino G.
    Int J Mol Sci; 2017 Nov 10; 18(11):. PubMed ID: 29125546
    [Abstract] [Full Text] [Related]

  • 2. AQP2: Mutations Associated with Congenital Nephrogenic Diabetes Insipidus and Regulation by Post-Translational Modifications and Protein-Protein Interactions.
    Gao C, Higgins PJ, Zhang W.
    Cells; 2020 Sep 26; 9(10):. PubMed ID: 32993088
    [Abstract] [Full Text] [Related]

  • 3. Physiopathology and diagnosis of nephrogenic diabetes insipidus.
    Devuyst O.
    Ann Endocrinol (Paris); 2012 Apr 26; 73(2):128-9. PubMed ID: 22503803
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  • 6. Nephrogenic diabetes insipidus: essential insights into the molecular background and potential therapies for treatment.
    Moeller HB, Rittig S, Fenton RA.
    Endocr Rev; 2013 Apr 26; 34(2):278-301. PubMed ID: 23360744
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  • 7. V2R mutations and nephrogenic diabetes insipidus.
    Bichet DG.
    Prog Mol Biol Transl Sci; 2009 Apr 26; 89():15-29. PubMed ID: 20374732
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  • 8. Nephrogenic diabetes insipidus.
    Bichet DG.
    Am J Med; 1998 Nov 26; 105(5):431-42. PubMed ID: 9831428
    [Abstract] [Full Text] [Related]

  • 9. Cell biological aspects of the vasopressin type-2 receptor and aquaporin 2 water channel in nephrogenic diabetes insipidus.
    Robben JH, Knoers NV, Deen PM.
    Am J Physiol Renal Physiol; 2006 Aug 26; 291(2):F257-70. PubMed ID: 16825342
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  • 10. Genetic basis of nephrogenic diabetes insipidus.
    Hureaux M, Vargas-Poussou R.
    Mol Cell Endocrinol; 2023 Jan 15; 560():111825. PubMed ID: 36460218
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  • 11. Hereditary nephrogenic diabetes insipidus in Japanese patients: analysis of 78 families and report of 22 new mutations in AVPR2 and AQP2.
    Sasaki S, Chiga M, Kikuchi E, Rai T, Uchida S.
    Clin Exp Nephrol; 2013 Jun 15; 17(3):338-44. PubMed ID: 23150186
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  • 12. [Nephrogenic diabetes insipidus].
    Evrard A, Lefebvre J, Vantyghem M.
    Ann Endocrinol (Paris); 1999 Dec 15; 60(6):457-64. PubMed ID: 10617799
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  • 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 15; 36(11):e22583. PubMed ID: 36197017
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  • 14. Nephrogenic Diabetes Insipidus.
    Balla A, Hunyady L.
    Exp Suppl; 2019 Nov 15; 111():317-339. PubMed ID: 31588538
    [Abstract] [Full Text] [Related]

  • 15. Congenital nephrogenic diabetes insipidus: the current state of affairs.
    Wesche D, Deen PM, Knoers NV.
    Pediatr Nephrol; 2012 Dec 15; 27(12):2183-204. PubMed ID: 22427315
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  • 16. [Clinical and laboratory characteristics of arginine vasopressin resistance, caused by a new homozygous mutation p.R113C in AQP2].
    Makretskaya NA, Nanzanova US, Hamaganova IR, Eremina ER, Tiulpakov AN.
    Probl Endokrinol (Mosk); 2023 May 12; 69(2):75-79. PubMed ID: 37448274
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  • 17. A female with X-linked Nephrogenic diabetes insipidus in a family with inherited central diabetes Insipidus: Case report and review of the literature.
    Ding C, Beetz R, Rittner G, Bartsch O.
    Am J Med Genet A; 2020 May 12; 182(5):1032-1040. PubMed ID: 32073219
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  • 18. Aquaporin 2 mutations in nephrogenic diabetes insipidus.
    Loonen AJ, Knoers NV, van Os CH, Deen PM.
    Semin Nephrol; 2008 May 12; 28(3):252-65. PubMed ID: 18519086
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  • 19. [Vasopressin V2 receptor-related pathologies: congenital nephrogenic diabetes insipidus and nephrogenic syndrome of inappropiate antidiuresis].
    Morin D.
    Nephrol Ther; 2014 Dec 12; 10(7):538-46. PubMed ID: 25449762
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