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3. 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]
4. An improved terminology and classification of Bartter-like syndromes. Seyberth HW Nat Clin Pract Nephrol; 2008 Oct; 4(10):560-7. PubMed ID: 18695706 [TBL] [Abstract][Full Text] [Related]
5. The molecular genetic approach to "Bartter's syndrome". Károlyi L; Koch MC; Grzeschik KH; Seyberth HW J Mol Med (Berl); 1998 Apr; 76(5):317-25. PubMed ID: 9587066 [TBL] [Abstract][Full Text] [Related]
6. [Bartter's syndrome]. Daniluk U; Kaczmarski M; Wasilewska J; Matuszewska E; Semeniuk J; Sidor K; Krasnow A Pol Merkur Lekarski; 2004 May; 16(95):484-9. PubMed ID: 15518434 [TBL] [Abstract][Full Text] [Related]
7. Mutations in the chloride channel gene CLCNKB as a cause of classic Bartter syndrome. Konrad M; Vollmer M; Lemmink HH; VAN DEN Heuvel LPWJ; Jeck N; Vargas-Poussou R; Lakings A; Ruf R; Deschênes G; Antignac C; Guay-Woodford L; Knoers NVAM; Seyberth HW; Feldmann D; Hildebrandt F J Am Soc Nephrol; 2000 Aug; 11(8):1449-1459. PubMed ID: 10906158 [TBL] [Abstract][Full Text] [Related]
9. Mouse model of type II Bartter's syndrome. II. Altered expression of renal sodium- and water-transporting proteins. Wagner CA; Loffing-Cueni D; Yan Q; Schulz N; Fakitsas P; Carrel M; Wang T; Verrey F; Geibel JP; Giebisch G; Hebert SC; Loffing J Am J Physiol Renal Physiol; 2008 Jun; 294(6):F1373-80. PubMed ID: 18322017 [TBL] [Abstract][Full Text] [Related]
10. Heterozygous mutations of the gene for Kir 1.1 (ROMK) in antenatal Bartter syndrome presenting with transient hyperkalemia, evolving to a benign course. Cho JT; Guay-Woodford LM J Korean Med Sci; 2003 Feb; 18(1):65-8. PubMed ID: 12589089 [TBL] [Abstract][Full Text] [Related]
11. Barttin increases surface expression and changes current properties of ClC-K channels. Waldegger S; Jeck N; Barth P; Peters M; Vitzthum H; Wolf K; Kurtz A; Konrad M; Seyberth HW Pflugers Arch; 2002 Jun; 444(3):411-8. PubMed ID: 12111250 [TBL] [Abstract][Full Text] [Related]
13. Mouse model of type II Bartter's syndrome. I. Upregulation of thiazide-sensitive Na-Cl cotransport activity. Cantone A; Yang X; Yan Q; Giebisch G; Hebert SC; Wang T Am J Physiol Renal Physiol; 2008 Jun; 294(6):F1366-72. PubMed ID: 18385266 [TBL] [Abstract][Full Text] [Related]
14. Mutations in the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Bartter syndrome: evidence for genetic heterogeneity. International Collaborative Study Group for Bartter-like Syndromes. Hum Mol Genet; 1997 Jan; 6(1):17-26. PubMed ID: 9002665 [TBL] [Abstract][Full Text] [Related]
16. Expression of the Na-K-2Cl cotransporter by macula densa and thick ascending limb cells of rat and rabbit nephron. Obermüller N; Kunchaparty S; Ellison DH; Bachmann S J Clin Invest; 1996 Aug; 98(3):635-40. PubMed ID: 8698854 [TBL] [Abstract][Full Text] [Related]
17. [Gitelman syndrome. An overlooked disease with chronic hypomagnesemia and hypokalemia in adults]. Hansen KW; Mosekilde L Ugeskr Laeger; 2003 Mar; 165(11):1123-7. PubMed ID: 12677988 [TBL] [Abstract][Full Text] [Related]
18. Late-onset manifestation of antenatal Bartter syndrome as a result of residual function of the mutated renal Na+-K+-2Cl- co-transporter. Pressler CA; Heinzinger J; Jeck N; Waldegger P; Pechmann U; Reinalter S; Konrad M; Beetz R; Seyberth HW; Waldegger S J Am Soc Nephrol; 2006 Aug; 17(8):2136-42. PubMed ID: 16807401 [TBL] [Abstract][Full Text] [Related]
19. Potassium handling in health and disease: lessons from inherited tubulopathies. Landau D Pediatr Endocrinol Rev; 2004 Dec; 2(2):203-8. PubMed ID: 16429107 [TBL] [Abstract][Full Text] [Related]
20. Generation and analyses of R8L barttin knockin mouse. Nomura N; Tajima M; Sugawara N; Morimoto T; Kondo Y; Ohno M; Uchida K; Mutig K; Bachmann S; Soleimani M; Ohta E; Ohta A; Sohara E; Okado T; Rai T; Jentsch TJ; Sasaki S; Uchida S Am J Physiol Renal Physiol; 2011 Aug; 301(2):F297-307. PubMed ID: 21593186 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]