220 related articles for article (PubMed ID: 8954067)
1. Association of a mutation in thiazide-sensitive Na-Cl cotransporter with familial Gitelman's syndrome.
Takeuchi K; Kure S; Kato T; Taniyama Y; Takahashi N; Ikeda Y; Abe T; Narisawa K; Muramatsu Y; Abe K
J Clin Endocrinol Metab; 1996 Dec; 81(12):4496-9. PubMed ID: 8954067
[TBL] [Abstract][Full Text] [Related]
2. Identification of a novel R642C mutation in Na/Cl cotransporter with Gitelman's syndrome.
Yahata K; Tanaka I; Kotani M; Mukoyama M; Ogawa Y; Goto M; Nakagawa M; Sugawara A; Tanaka K; Shimatsu A; Nakao K
Am J Kidney Dis; 1999 Nov; 34(5):845-53. PubMed ID: 10561140
[TBL] [Abstract][Full Text] [Related]
3. Three cases of Gitelman's syndrome possibly caused by different mutations in the thiazide-sensitive Na-Cl cotransporter.
Takeuchi K; Kato T; Taniyama Y; Tsunoda K; Takahashi N; Ikeda Y; Omata K; Imai Y; Saito T; Ito S; Abe K
Intern Med; 1997 Aug; 36(8):582-5. PubMed ID: 9260778
[TBL] [Abstract][Full Text] [Related]
4. Attenuated renal excretion in response to thiazide diuretics in Gitelman's syndrome: a case report.
Yeum CH; Kim SW; Ma SK; Ko JH; Nah MY; Kim NH; Choi KC
J Korean Med Sci; 2002 Aug; 17(4):567-70. PubMed ID: 12172059
[TBL] [Abstract][Full Text] [Related]
5. Abnormal reabsorption of Na+/CI- by the thiazide-inhibitable transporter of the distal convoluted tubule in Gitelman's syndrome.
Colussi G; Rombolà G; Brunati C; De Ferrari ME
Am J Nephrol; 1997; 17(2):103-11. PubMed ID: 9096439
[TBL] [Abstract][Full Text] [Related]
6. Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter.
Simon DB; Nelson-Williams C; Bia MJ; Ellison D; Karet FE; Molina AM; Vaara I; Iwata F; Cushner HM; Koolen M; Gainza FJ; Gitleman HJ; Lifton RP
Nat Genet; 1996 Jan; 12(1):24-30. PubMed ID: 8528245
[TBL] [Abstract][Full Text] [Related]
7. [Renal sodium transport abnormality: Gitelman's syndrome and renal sodium transporter].
Takeuchi K; Taniyama Y; Ito S; Yasujima M
Rinsho Byori; 1999 Dec; 47(12):1128-33. PubMed ID: 10639822
[TBL] [Abstract][Full Text] [Related]
8. Mimicry of surreptitious diuretic ingestion and the ability to make a genetic diagnosis.
Schepkens H; Hoeben H; Vanholder R; Lameire N
Clin Nephrol; 2001 Mar; 55(3):233-7. PubMed ID: 11316244
[TBL] [Abstract][Full Text] [Related]
9. Novel mutations in thiazide-sensitive Na-Cl cotransporter gene of patients with Gitelman's syndrome.
Monkawa T; Kurihara I; Kobayashi K; Hayashi M; Saruta T
J Am Soc Nephrol; 2000 Jan; 11(1):65-70. PubMed ID: 10616841
[TBL] [Abstract][Full Text] [Related]
10. Gitelman's syndrome (Bartter's variant) maps to the thiazide-sensitive cotransporter gene locus on chromosome 16q13 in a large kindred.
Pollak MR; Delaney VB; Graham RM; Hebert SC
J Am Soc Nephrol; 1996 Oct; 7(10):2244-8. PubMed ID: 8915985
[TBL] [Abstract][Full Text] [Related]
11. Genetic variants of thiazide-sensitive NaCl-cotransporter in Gitelman's syndrome and primary hypertension.
Melander O; Orho-Melander M; Bengtsson K; Lindblad U; Râstam L; Groop L; Hulthén UL
Hypertension; 2000 Sep; 36(3):389-94. PubMed ID: 10988270
[TBL] [Abstract][Full Text] [Related]
12. Gitelman's syndrome (familial hypokalemia-hypomagnesemia).
Barakat AJ; Rennert OM
J Nephrol; 2001; 14(1):43-7. PubMed ID: 11281344
[TBL] [Abstract][Full Text] [Related]
13. The molecular basis of inherited hypokalemic alkalosis: Bartter's and Gitelman's syndromes.
Simon DB; Lifton RP
Am J Physiol; 1996 Nov; 271(5 Pt 2):F961-6. PubMed ID: 8945989
[TBL] [Abstract][Full Text] [Related]
14. Miscellaneous non-inflammatory musculoskeletal conditions. Bartter's and Gitelman's diseases.
Favero M; Calò LA; Schiavon F; Punzi L
Best Pract Res Clin Rheumatol; 2011 Oct; 25(5):637-48. PubMed ID: 22142744
[TBL] [Abstract][Full Text] [Related]
15. Gitelman's syndrome with mental retardation.
Morita R; Takeuchi K; Nakamura A; Tajima T; Kuroda Y
Intern Med; 2006; 45(4):211-3. PubMed ID: 16543691
[TBL] [Abstract][Full Text] [Related]
16. Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2.
Simon DB; Karet FE; Hamdan JM; DiPietro A; Sanjad SA; Lifton RP
Nat Genet; 1996 Jun; 13(2):183-8. PubMed ID: 8640224
[TBL] [Abstract][Full Text] [Related]
17. [Gitelman's syndrome: an important differential diagnosis of hypokalemia].
Kurschat C; Heering P; Grabensee B
Dtsch Med Wochenschr; 2003 May; 128(22):1225-8. PubMed ID: 12772080
[TBL] [Abstract][Full Text] [Related]
18. Two novel genotypes of the thiazide-sensitive Na-Cl cotransporter (SLC12A3) gene in patients with Gitelman's syndrome.
Aoi N; Nakayama T; Tahira Y; Haketa A; Yabuki M; Sekiyama T; Nakane C; Mano H; Kawachi H; Sato N; Soma M; Matsumoto K
Endocrine; 2007 Apr; 31(2):149-53. PubMed ID: 17873326
[TBL] [Abstract][Full Text] [Related]
19. Phenotype resembling Gitelman's syndrome in mice lacking the apical Na+-Cl- cotransporter of the distal convoluted tubule.
Schultheis PJ; Lorenz JN; Meneton P; Nieman ML; Riddle TM; Flagella M; Duffy JJ; Doetschman T; Miller ML; Shull GE
J Biol Chem; 1998 Oct; 273(44):29150-5. PubMed ID: 9786924
[TBL] [Abstract][Full Text] [Related]
20. Defective processing and expression of thiazide-sensitive Na-Cl cotransporter as a cause of Gitelman's syndrome.
Kunchaparty S; Palcso M; Berkman J; Velázquez H; Desir GV; Bernstein P; Reilly RF; Ellison DH
Am J Physiol; 1999 Oct; 277(4):F643-9. PubMed ID: 10516289
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]