176 related articles for article (PubMed ID: 27577218)
1. [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]
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. [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]
4. [Identification of mutations in the arginine vasopressin receptor 2 gene in congenital nephrogenic diabetes insipidus patients].
Gu F; Shi Y; Deng J; Jin Z
Zhonghua Yi Xue Za Zhi; 2002 Oct; 82(20):1401-5. PubMed ID: 12509923
[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 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]
7. 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]
8. 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; 7():53. PubMed ID: 17101063
[TBL] [Abstract][Full Text] [Related]
9. Contiguous 22.1-kb deletion embracing AVPR2 and ARHGAP4 genes at novel breakpoints leads to nephrogenic diabetes insipidus in a Chinese pedigree.
Bai Y; Chen Y; Kong X
BMC Nephrol; 2018 Feb; 19(1):26. PubMed ID: 29394883
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. 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]
13. 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; 182(5):1032-1040. PubMed ID: 32073219
[TBL] [Abstract][Full Text] [Related]
14. Novel mutations associated with nephrogenic diabetes insipidus. A clinical-genetic study.
García Castaño A; Pérez de Nanclares G; Madariaga L; Aguirre M; Chocron S; Madrid A; Lafita Tejedor FJ; Gil Campos M; Sánchez Del Pozo J; Ruiz Cano R; Espino M; Gomez Vida JM; Santos F; García Nieto VM; Loza R; Rodríguez LM; Hidalgo Barquero E; Printza N; Camacho JA; Castaño L; Ariceta G;
Eur J Pediatr; 2015 Oct; 174(10):1373-85. PubMed ID: 25902753
[TBL] [Abstract][Full Text] [Related]
15. Clinical phenotype of nephrogenic diabetes insipidus in females heterozygous for a vasopressin type 2 receptor mutation.
van Lieburg AF; Verdijk MA; Schoute F; Ligtenberg MJ; van Oost BA; Waldhauser F; Dobner M; Monnens LA; Knoers NV
Hum Genet; 1995 Jul; 96(1):70-8. PubMed ID: 7607658
[TBL] [Abstract][Full Text] [Related]
16. Novel vasopressin type 2 (AVPR2) gene mutations in Brazilian nephrogenic diabetes insipidus patients.
Boson WL; Della Manna T; Damiani D; Miranda DM; Gadelha MR; Liberman B; Correa H; Romano-Silva MA; Friedman E; Silva FF; Ribeiro PA; De Marco L
Genet Test; 2006; 10(3):157-62. PubMed ID: 17020465
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. Novel AVPR2 mutation causing partial nephrogenic diabetes insipidus in a Japanese family.
Yamashita S; Hata A; Usui T; Oda H; Hijikata A; Shirai T; Kaneko N; Hata D
J Pediatr Endocrinol Metab; 2016 May; 29(5):591-6. PubMed ID: 26974133
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
