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24. 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]
25. Gitelman's syndrome is genetically distinct from other forms of Bartter's syndrome. Károlyi L; Ziegler A; Pollak M; Fischbach M; Grzeschik KH; Koch MC; Seyberth HW Pediatr Nephrol; 1996 Oct; 10(5):551-4. PubMed ID: 8897553 [TBL] [Abstract][Full Text] [Related]
26. Problems in diagnosing atypical Gitelman's syndrome presenting with normomagnesaemia. Nakamura A; Shimizu C; Nagai S; Yoshida M; Aoki K; Kondo T; Miyoshi H; Wada N; Tajima T; Terauchi Y; Yoshioka N; Koike T Clin Endocrinol (Oxf); 2010 Feb; 72(2):272-6. PubMed ID: 19508680 [TBL] [Abstract][Full Text] [Related]
27. Mutations in renal ion transporters cause Gitelman's and Bartter's syndromes of inherited hypokalemic alkalosis. Simon DB; Lifton RP Adv Nephrol Necker Hosp; 1997; 27():343-59. PubMed ID: 9408455 [No Abstract] [Full Text] [Related]
29. 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]
30. 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]
31. Hypokalemic nephropathy in an adult patient with partial empty sella: a classic Bartter's syndrome, a Gitelman's syndrome or both? Addolorato G; Ancarani F; Leggio L; Abenavoli L; de Lorenzi G; Montalto M; Staffolani E; Zannoni GF; Costanzi S; Gasbarrini G Panminerva Med; 2006 Jun; 48(2):137-42. PubMed ID: 16953151 [TBL] [Abstract][Full Text] [Related]
32. 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]
33. Ion transporter mutations in Gitelman's and Bartter's syndromes. Simon DB; Lifton RP Curr Opin Nephrol Hypertens; 1998 Jan; 7(1):43-7. PubMed ID: 9442362 [TBL] [Abstract][Full Text] [Related]
34. Chondrocalcinosis is a feature of Gitelman's variant of Bartter's syndrome. A new look at the hypomagnesemia associated with calcium pyrophosphate dihydrate crystal deposition disease. Punzi L; Calò L; Schiavon F; Pianon M; Rosada M; Todesco S Rev Rhum Engl Ed; 1998 Oct; 65(10):571-4. PubMed ID: 9809361 [TBL] [Abstract][Full Text] [Related]
35. Normal prostaglandinuria E2 in Gitelman's syndrome, the hypocalciuric variant of Bartter's syndrome. Lüthy C; Bettinelli A; Iselin S; Metta MG; Basilico E; Oetliker OH; Bianchetti MG Am J Kidney Dis; 1995 Jun; 25(6):824-8. PubMed ID: 7771477 [TBL] [Abstract][Full Text] [Related]
36. Clinical, biochemical and molecular genetic data in five children with Gitelman's syndrome. Schmidt H; Kabesch M; Schwarz HP; Kiess W Horm Metab Res; 2001 Jun; 33(6):354-7. PubMed ID: 11456284 [TBL] [Abstract][Full Text] [Related]
37. Analyses of subjects with hypokalemic metabolic alkolosis, Gitelman's and Bartter's syndrome. Onem Y; Kucukardali Y; Sahan B; Atasoyu EM; Ipcioğlu O; Terekeci H; Solmazgul E; Top C; Oktenli C Ren Fail; 2008; 30(7):691-4. PubMed ID: 18704817 [TBL] [Abstract][Full Text] [Related]
38. [Bartter's syndrome: new classification, old therapy]. Peco-Antic A; Dudic S; Marsenic O; Zivic G Srp Arh Celok Lek; 2001; 129(5-6):139-42. PubMed ID: 11797462 [TBL] [Abstract][Full Text] [Related]