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Journal Abstract Search

231 related items for PubMed ID: 19449677

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  • 2. 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; 8(12):1855-62. PubMed ID: 9402087
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  • 5. Novel and recurrent variants in AVPR2 in 19 families with X-linked congenital nephrogenic diabetes insipidus.
    Joshi S, Kvistgaard H, Kamperis K, Færch M, Hagstrøm S, Gregersen N, Rittig S, Christensen JH.
    Eur J Pediatr; 2018 Sep; 177(9):1399-1405. PubMed ID: 29594432
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  • 9. Deletion of the V2 vasopressin receptor gene in two Chinese patients with nephrogenic diabetes insipidus.
    Dong Y, Sheng H, Chen X, Yin J, Su Q.
    BMC Genet; 2006 Nov 14; 7():53. PubMed ID: 17101063
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  • 10. 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 14; 30(2):263-76. PubMed ID: 27156763
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  • 12. 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 14; 61(7):922-30. PubMed ID: 22386940
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  • 16. Six novel mutations in the vasopressin V2 receptor gene causing nephrogenic diabetes insipidus.
    Cheong HI, Park HW, Ha IS, Moon HN, Choi Y, Ko KW, Jun JK.
    Nephron; 1997 Jul 14; 75(4):431-7. PubMed ID: 9127330
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