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10. C112R, W323S, N317K mutations in the vasopressin V2 receptor gene in patients with nephrogenic diabetes insipidus. Mutations in brief no. 165. Online. Szalai C; Triga D; Czinner A Hum Mutat; 1998; 12(2):137-8. PubMed ID: 10694923 [TBL] [Abstract][Full Text] [Related]
11. Autosomal recessive nephrogenic diabetes insipidus caused by an aquaporin-2 mutation. Hochberg Z; Van Lieburg A; Even L; Brenner B; Lanir N; Van Oost BA; Knoers NV J Clin Endocrinol Metab; 1997 Feb; 82(2):686-9. PubMed ID: 9024277 [TBL] [Abstract][Full Text] [Related]
12. Normal response of factor VIII and von Willebrand factor to 1-deamino-8D-arginine vasopressin in nephrogenic diabetes insipidus. Brenner B; Seligsohn U; Hochberg Z J Clin Endocrinol Metab; 1988 Jul; 67(1):191-3. PubMed ID: 3132483 [TBL] [Abstract][Full Text] [Related]
13. Mutations in the vasopressin V2 receptor gene in families with nephrogenic diabetes insipidus and functional expression of the Q-2 mutant. Rosenthal W; Seibold A; Antaramian A; Gilbert S; Birnbaumer M; Bichet DG; Arthus MF; Lonergan M Cell Mol Biol (Noisy-le-grand); 1994 May; 40(3):429-36. PubMed ID: 7920187 [TBL] [Abstract][Full Text] [Related]
14. Detection of skewed X-inactivation in two female carriers of vasopressin type 2 receptor gene mutation. Nomura Y; Onigata K; Nagashima T; Yutani S; Mochizuki H; Nagashima K; Morikawa A J Clin Endocrinol Metab; 1997 Oct; 82(10):3434-7. PubMed ID: 9329382 [TBL] [Abstract][Full Text] [Related]
15. A Novel Form of Familial Vasopressin Deficient Diabetes Insipidus Transmitted in an X-linked Recessive Manner. Habiby R; Bichet DG; Arthus MF; Connaughton D; Shril S; Mane S; Majmundar AJ; Hildebrandt F; Robertson GL J Clin Endocrinol Metab; 2022 May; 107(6):e2513-e2522. PubMed ID: 35137152 [TBL] [Abstract][Full Text] [Related]
16. Lack of responsiveness to 1-desamino-D arginin vasopressin (desmopressin) in male patients with nephrogenic syndrome of inappropriate antidiuresis: from bench to bedside. Vandergheynst F; Pradier O; Beukinga I; Kornreich A; Vassart G; Decaux G Eur J Clin Invest; 2012 Mar; 42(3):254-9. PubMed ID: 21834801 [TBL] [Abstract][Full Text] [Related]
18. Novel mutations in the V2 vasopressin receptor gene in two pedigrees with congenital nephrogenic diabetes insipidus. Yuasa H; Ito M; Oiso Y; Kurokawa M; Watanabe T; Oda Y; Ishizuka T; Tani N; Ito S; Shibata A J Clin Endocrinol Metab; 1994 Aug; 79(2):361-5. PubMed ID: 8045948 [TBL] [Abstract][Full Text] [Related]
19. A low affinity vasopressin V2-receptor in inherited nephrogenic diabetes insipidus. Luzius H; Jans DA; Grünbaum EG; Moritz A; Rascher W; Fahrenholz F J Recept Res; 1992; 12(3):351-68. PubMed ID: 1387165 [TBL] [Abstract][Full Text] [Related]
20. Molecular identification of the gene responsible for congenital nephrogenic diabetes insipidus. Rosenthal W; Seibold A; Antaramian A; Lonergan M; Arthus MF; Hendy GN; Birnbaumer M; Bichet DG Nature; 1992 Sep; 359(6392):233-5. PubMed ID: 1356229 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]