189 related articles for article (PubMed ID: 33125666)
1. 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]
2. 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]
3. 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]
4. 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]
5. A novel mutation in the AVPR2 gene (222delA) associated with X-linked nephrogenic diabetes insipidus in a boy with growth failure.
Abaci A; Wood K; Demir K; Büyükgebiz A; Böber E; Kopp P
Endocr Pract; 2010; 16(2):231-6. PubMed ID: 19703807
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. [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]
8. 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]
9. 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]
10. A large deletion of the AVPR2 gene causing severe nephrogenic diabetes insipidus in a Turkish family.
Saglar E; Deniz F; Erdem B; Karaduman T; Yönem A; Cagiltay E; Mergen H
Endocrine; 2014 May; 46(1):148-53. PubMed ID: 24026507
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Physiopathology and diagnosis of nephrogenic diabetes insipidus.
Devuyst O
Ann Endocrinol (Paris); 2012 Apr; 73(2):128-9. PubMed ID: 22503803
[TBL] [Abstract][Full Text] [Related]
14. A novel AVPR2 missense mutation in a Chinese boy with severe inherited nephrogenic diabetes insipidus.
Huang L; Li W; Tang W; Lu G
J Pediatr Endocrinol Metab; 2011; 24(9-10):807-9. PubMed ID: 22145481
[TBL] [Abstract][Full Text] [Related]
15. V2R mutations and nephrogenic diabetes insipidus.
Bichet DG
Prog Mol Biol Transl Sci; 2009; 89():15-29. PubMed ID: 20374732
[TBL] [Abstract][Full Text] [Related]
16. 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; 18(11):. PubMed ID: 29125546
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. [Vasopressin V2 receptor-related pathologies: congenital nephrogenic diabetes insipidus and nephrogenic syndrome of inappropiate antidiuresis].
Morin D
Nephrol Ther; 2014 Dec; 10(7):538-46. PubMed ID: 25449762
[TBL] [Abstract][Full Text] [Related]
19. Functional characterization of vasopressin receptor 2 mutations causing partial and complete congenital nephrogenic diabetes insipidus in Thai families.
Sahakitrungruang T; Tee MK; Rattanachartnarong N; Shotelersuk V; Suphapeetiporn K; Miller WL
Horm Res Paediatr; 2010; 73(5):349-54. PubMed ID: 20389105
[TBL] [Abstract][Full Text] [Related]
20. Nephrogenic diabetes insipidus.
Bichet DG
Adv Chronic Kidney Dis; 2006 Apr; 13(2):96-104. PubMed ID: 16580609
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
