Literature DB >> 15851323

Congenital long QT syndrome aggravated by salt-wasting nephropathy.

Dawood Darbar1, Saba Sile, Frank A Fish, Alfred L George.   

Abstract

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Mesh：

Year:  2005        PMID： 15851323      PMCID： PMC1350445          DOI： 10.1016/j.hrthm.2004.11.015

Source DB:  PubMed          Journal:  Heart Rhythm        ISSN： 1547-5271            Impact factor:   6.343


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  15 in total

1.  A novel mutation in the chloride channel gene, CLCNKB, as a cause of Gitelman and Bartter syndromes.

Authors:  Israel Zelikovic; Raymonde Szargel; Ali Hawash; Valentina Labay; Ihab Hatib; Nadine Cohen; Farid Nakhoul
Journal:  Kidney Int       Date:  2003-01       Impact factor: 10.612

2.  Allelic variants in long-QT disease genes in patients with drug-associated torsades de pointes.

Authors:  Ping Yang; Hideaki Kanki; Benoit Drolet; Tao Yang; Jian Wei; Prakash C Viswanathan; Stefan H Hohnloser; Wataru Shimizu; Peter J Schwartz; Marshall Stanton; Katherine T Murray; Kris Norris; Alfred L George; Dan M Roden
Journal:  Circulation       Date:  2002-04-23       Impact factor: 29.690

3.  KVLQT1 C-terminal missense mutation causes a forme fruste long-QT syndrome.

Authors:  C Donger; I Denjoy; M Berthet; N Neyroud; C Cruaud; M Bennaceur; G Chivoret; K Schwartz; P Coumel; P Guicheney
Journal:  Circulation       Date:  1997-11-04       Impact factor: 29.690

4.  A structural basis for drug-induced long QT syndrome.

Authors:  J S Mitcheson; J Chen; M Lin; C Culberson; M C Sanguinetti
Journal:  Proc Natl Acad Sci U S A       Date:  2000-10-24       Impact factor: 11.205

Review 5.  Congenital and acquired long QT syndrome. Current concepts and management.

Authors:  Chern-En Chiang
Journal:  Cardiol Rev       Date:  2004 Jul-Aug       Impact factor: 2.644

6.  Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter.

Authors:  D B Simon; C Nelson-Williams; M J Bia; D Ellison; F E Karet; A M Molina; I Vaara; F Iwata; H M Cushner; M Koolen; F J Gainza; H J Gitleman; R P Lifton
Journal:  Nat Genet       Date:  1996-01       Impact factor: 38.330

Review 7.  Prevention of cardiac arrhythmias in pediatric patients with normotensive-hypokalemic tubulopathy. Current attitude among European pediatricians.

Authors:  Cinzia Cortesi; Pietro E G Foglia; Alberto Bettinelli; Mario G Bianchetti
Journal:  Pediatr Nephrol       Date:  2003-08       Impact factor: 3.714

8.  Extracellular potassium modulation of drug block of IKr. Implications for torsade de pointes and reverse use-dependence.

Authors:  T Yang; D M Roden
Journal:  Circulation       Date:  1996-02-01       Impact factor: 29.690

9.  Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia.

Authors:  Igor Splawski; Katherine W Timothy; Michihiro Tateyama; Colleen E Clancy; Alka Malhotra; Alan H Beggs; Francesco P Cappuccio; Giuseppe A Sagnella; Robert S Kass; Mark T Keating
Journal:  Science       Date:  2002-08-23       Impact factor: 47.728

10.  A new oral therapy for long QT syndrome: long-term oral potassium improves repolarization in patients with HERG mutations.

Authors:  Susan P Etheridge; Steven J Compton; Martin Tristani-Firouzi; Jay W Mason
Journal:  J Am Coll Cardiol       Date:  2003-11-19       Impact factor: 24.094
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  1 in total

1.  Cardiac arrhythmias and rhabdomyolysis in Bartter-Gitelman patients.

Authors:  Cinzia Cortesi; Sebastiano A G Lava; Alberto Bettinelli; Fabiana Tammaro; Olivier Giannini; Maria Caiata-Zufferey; Mario G Bianchetti
Journal:  Pediatr Nephrol       Date:  2010-06-13       Impact factor: 3.714
  1 in total

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