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Results: 1 to 20 of 34

Related Articles by Review for PubMed (Select 8640224)

1.

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.

PMID:
8640224
2.

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. Review.

PMID:
8945989
3.

Mutations in Na(K)Cl transporters in Gitelman's and Bartter's syndromes.

Simon DB, Lifton RP.

Curr Opin Cell Biol. 1998 Aug;10(4):450-4. Review.

PMID:
9719864
4.

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. doi: 10.1016/j.berh.2011.10.013. Review.

PMID:
22142744
5.

[Bartter's syndromes].

Vantyghem MC, Douillard C, Binaut R, Provot F.

Ann Endocrinol (Paris). 1999 Dec;60(6):465-72. Review. French.

PMID:
10617800
6.

Bartter's and Gitelman's syndromes: from gene to clinic.

Naesens M, Steels P, Verberckmoes R, Vanrenterghem Y, Kuypers D.

Nephron Physiol. 2004;96(3):p65-78. Review.

PMID:
15056980
7.
8.

Molecular pathogenesis of Bartter's and Gitelman's syndromes.

Kurtz I.

Kidney Int. 1998 Oct;54(4):1396-410. Review. No abstract available.

9.

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. Review.

PMID:
9587066
10.

[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. Review. Polish.

PMID:
15518434
11.

Regulation of the renal Na/K/2Cl cotransporter gene. Physiological modulation in health and abnormal function in disease.

Nonoguchi H, Itoh K, Ikebe M, Tomita K.

Exp Nephrol. 1998 Jul-Aug;6(4):272-6. Review.

PMID:
9690088
12.

Ion transporter mutations in Gitelman's and Bartter's syndromes.

Simon DB, Lifton RP.

Curr Opin Nephrol Hypertens. 1998 Jan;7(1):43-7. Review.

PMID:
9442362
13.

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. Review. No abstract available.

PMID:
9408455
14.

Chloride channels in renal disease.

Thakker RV.

Adv Nephrol Necker Hosp. 1999;29:289-98. Review.

PMID:
10561751
15.
16.

[Bartter's syndrome and Gitelman's syndrome: Pathogenesis, pathophysiology, and therapy].

Watanabe S, Uchida S.

Nihon Rinsho. 2006 Feb;64 Suppl 2:504-7. Review. Japanese.

PMID:
16523943
17.

[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. Review. Japanese.

PMID:
10639822
19.

Molecular pathology of renal chloride channels in Dent's disease and Bartter's syndrome.

Thakker RV.

Exp Nephrol. 2000 Nov-Dec;8(6):351-60. Review.

PMID:
11014932
20.

The molecular physiology of electroneutral cation-chloride cotransport.

Mount DB, Hoover RS, Hebert SC.

J Membr Biol. 1997 Aug 1;158(3):177-86. Review.

PMID:
9263880
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