BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

142 related articles for article (PubMed ID: 34619845)

  • 1. [Clinical characteristics of congenital nephrogenic diabetes insipidus].
    Zhang YH; Li ZZ; Li S; Meng DD; Qin GJ
    Zhonghua Nei Ke Za Zhi; 2021 Jul; 60(7):665-668. PubMed ID: 34619845
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Congenital nephrogenic diabetes insipidus accompanied with central nephrogenic diabetes secondary to pituitary surgery -a case report.
    Zhang W; Shen Y; Ren Y; Xin Y; Wang L
    BMC Endocr Disord; 2021 Apr; 21(1):78. PubMed ID: 33882907
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A Novel Mutation in the
    Çelebi Tayfur A; Karaduman T; Özcan Türkmen M; Şahin D; Çaltık Yılmaz A; Büyükkaragöz B; Buluş AD; Mergen H
    J Clin Res Pediatr Endocrinol; 2018 Nov; 10(4):350-356. PubMed ID: 29991464
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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; 44(5):1131-1137. PubMed ID: 27565746
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A Novel Missense Mutation of Arginine Vasopressin Receptor 2 in a Chinese Family with Congenital Nephrogenic Diabetes Insipidus: X-Chromosome Inactivation in Female CNDI Patients with Heterozygote 814A>G Mutation.
    Zang L; Gong Y; Li Y; Dou J; Lyu Z; Su X; Zhang Y; Mu Y
    Biomed Res Int; 2022; 2022():7073158. PubMed ID: 35865667
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Nephrogenic diabetes insipidus due to a novel AVPR2 mutation.
    Sakallioglu O; Tascilar ME; Kalman S; Cheong HI; Atay AA
    J Pediatr Endocrinol Metab; 2009 Feb; 22(2):187-9. PubMed ID: 19449677
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Partial nephrogenic diabetes insipidus caused by a novel mutation in the AVPR2 gene.
    Faerch M; Christensen JH; Corydon TJ; Kamperis K; de Zegher F; Gregersen N; Robertson GL; Rittig S
    Clin Endocrinol (Oxf); 2008 Mar; 68(3):395-403. PubMed ID: 17941907
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Novel AVPR2 mutations and clinical characteristics in 28 Chinese families with congenital nephrogenic diabetes insipidus.
    Li Q; Tian D; Cen J; Duan L; Xia W
    J Endocrinol Invest; 2021 Dec; 44(12):2777-2783. PubMed ID: 34101133
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic analysis of a congenital nephrogenic diabetes insipidus pedigree.
    Shen Y; Lai X; Xiao X; Li J; Yu R; Gao H; Zhang M
    Chin Med J (Engl); 2014; 127(6):1089-92. PubMed ID: 24622440
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A patient with congenital nephrogenic diabetes insipidus due to AVPR2 mutation complicated by persisting polydipsia under hemodialysis treatment.
    Iijima T; Mori T; Sohara E; Suwabe T; Hoshino J; Ubara Y
    CEN Case Rep; 2021 May; 10(2):226-229. PubMed ID: 33125666
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A novel AVPR2 splice site mutation leads to partial X-linked nephrogenic diabetes insipidus in two brothers.
    Schernthaner-Reiter MH; Adams D; Trivellin G; Ramnitz MS; Raygada M; Golas G; Faucz FR; Nilsson O; Nella AA; Dileepan K; Lodish M; Lee P; Tifft C; Markello T; Gahl W; Stratakis CA
    Eur J Pediatr; 2016 May; 175(5):727-33. PubMed ID: 26795631
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Analysis of AVPR2 variant in a neonate with congenital nephrogenic diabetes insipidus].
    Yu Y; Chen A; Zheng J; Chen L; Du L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Dec; 37(12):1376-1379. PubMed ID: 33306826
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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; 30(2):263-76. PubMed ID: 27156763
    [TBL] [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; 8(12):1855-62. PubMed ID: 9402087
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Analysis of AVPR2 gene mutation in a pedigree affected with congenital nephrogenic diabetes insipidus].
    Dai Z; Ruan L; Jin J; Qian Y; Wang L; Shi Z; Wu C
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Oct; 33(5):666-9. PubMed ID: 27577218
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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; 47(1):126-30. PubMed ID: 16502494
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Correlation between AVPR2 mutations and urinary AQP2 excretion in patients with nephrogenic diabetes insipidus.
    Kotnik P; Battelino T; Debeljak M; Podkrajsek KT; Waldhauser F; Frøkiaer J; Nielsen S; Krzisnik C
    J Pediatr Endocrinol Metab; 2007 Apr; 20(4):483-9. PubMed ID: 17550212
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A 4-year-old boy presenting with persistent urinary incontinence: Questions.
    Keenswijk W; Walle JV
    Pediatr Nephrol; 2017 May; 32(5):767-768. PubMed ID: 27350623
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.