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Items: 1 to 20 of 411

1.

ECG T-wave patterns in genetically distinct forms of the hereditary long QT syndrome.

Moss AJ, Zareba W, Benhorin J, Locati EH, Hall WJ, Robinson JL, Schwartz PJ, Towbin JA, Vincent GM, Lehmann MH.

Circulation. 1995 Nov 15;92(10):2929-34.

2.

Age-gender influence on the rate-corrected QT interval and the QT-heart rate relation in families with genotypically characterized long QT syndrome.

Lehmann MH, Timothy KW, Frankovich D, Fromm BS, Keating M, Locati EH, Taggart RT, Towbin JA, Moss AJ, Schwartz PJ, Vincent GM.

J Am Coll Cardiol. 1997 Jan;29(1):93-9.

3.

Genetically defined therapy of inherited long-QT syndrome. Correction of abnormal repolarization by potassium.

Compton SJ, Lux RL, Ramsey MR, Strelich KR, Sanguinetti MC, Green LS, Keating MT, Mason JW.

Circulation. 1996 Sep 1;94(5):1018-22.

4.

Spectrum of ST-T-wave patterns and repolarization parameters in congenital long-QT syndrome: ECG findings identify genotypes.

Zhang L, Timothy KW, Vincent GM, Lehmann MH, Fox J, Giuli LC, Shen J, Splawski I, Priori SG, Compton SJ, Yanowitz F, Benhorin J, Moss AJ, Schwartz PJ, Robinson JL, Wang Q, Zareba W, Keating MT, Towbin JA, Napolitano C, Medina A.

Circulation. 2000 Dec 5;102(23):2849-55.

5.

The LQT syndromes--current status of molecular mechanisms.

Schulze-Bahr E, Wedekind H, Haverkamp W, Borggrefe M, Assmann G, Breithardt G, Funke H.

Z Kardiol. 1999 Apr;88(4):245-54. Review.

PMID:
10408028
7.

Genotype-specific ECG patterns in long QT syndrome.

Zareba W.

J Electrocardiol. 2006 Oct;39(4 Suppl):S101-6. Epub 2006 Sep 11. Review.

PMID:
16963070
8.

T wave "humps" as a potential electrocardiographic marker of the long QT syndrome.

Lehmann MH, Suzuki F, Fromm BS, Frankovich D, Elko P, Steinman RT, Fresard J, Baga JJ, Taggart RT.

J Am Coll Cardiol. 1994 Sep;24(3):746-54.

9.

A mutation in HERG associated with notched T waves in long QT syndrome.

Dausse E, Berthet M, Denjoy I, André-Fouet X, Cruaud C, Bennaceur M, Fauré S, Coumel P, Schwartz K, Guicheney P.

J Mol Cell Cardiol. 1996 Aug;28(8):1609-15.

PMID:
8877771
10.

A case of term mors in utero in a chromosome 11p linked long QT syndrome family.

Desmyttere S, Bonduelle M, De Wolf D, Liebaers I, Lissens W.

Genet Couns. 1994;5(3):289-95.

PMID:
7811430
11.

Exercise stress test amplifies genotype-phenotype correlation in the LQT1 and LQT2 forms of the long-QT syndrome.

Takenaka K, Ai T, Shimizu W, Kobori A, Ninomiya T, Otani H, Kubota T, Takaki H, Kamakura S, Horie M.

Circulation. 2003 Feb 18;107(6):838-44.

12.

Electrocardiographic features in Andersen-Tawil syndrome patients with KCNJ2 mutations: characteristic T-U-wave patterns predict the KCNJ2 genotype.

Zhang L, Benson DW, Tristani-Firouzi M, Ptacek LJ, Tawil R, Schwartz PJ, George AL, Horie M, Andelfinger G, Snow GL, Fu YH, Ackerman MJ, Vincent GM.

Circulation. 2005 May 31;111(21):2720-6. Epub 2005 May 23.

13.

Diagnostic performance of QT interval variables from 24-h electrocardiography in the long QT syndrome.

Neyroud N, Maison-Blanche P, Denjoy I, Chevret S, Donger C, Dausse E, Fayn J, Badilini F, Menhabi N, Schwartz K, Guicheney P, Coumel P.

Eur Heart J. 1998 Jan;19(1):158-65.

PMID:
9503190
14.

Genetics, molecular mechanisms and management of long QT syndrome.

Wang Q, Chen Q, Towbin JA.

Ann Med. 1998 Feb;30(1):58-65. Review.

PMID:
9556090
15.

Repolarization dynamics in patients with long QT syndrome.

Perkiömäki JS, Zareba W, Nomura A, Andrews M, Kaufman ES, Moss AJ.

J Cardiovasc Electrophysiol. 2002 Jul;13(7):651-6.

PMID:
12139286
16.

Diagnostic accuracy of screening electrocardiograms in long QT syndrome I.

Miller MD, Porter Cb, Ackerman MJ.

Pediatrics. 2001 Jul;108(1):8-12.

PMID:
11433047
17.

[Molecular genetics of the long QT syndrome. Genes causing syncope and sudden death].

Fosdal I, Wettrell G, Christiansen M, Kanters JK, Larsen LA.

Lakartidningen. 2001 Feb 21;98(8):810-5. Review. Swedish.

PMID:
11265565
19.

Arrhythmic disorder mapped to chromosome 1q42-q43 causes malignant polymorphic ventricular tachycardia in structurally normal hearts.

Swan H, Piippo K, Viitasalo M, Heikkilä P, Paavonen T, Kainulainen K, Kere J, Keto P, Kontula K, Toivonen L.

J Am Coll Cardiol. 1999 Dec;34(7):2035-42.

20.

Clinical characteristics of 5 Chinese LQTS families and phenotype-genotype correlation.

Lian J, Cui C, Xue X, Huang C, Cui H.

J Huazhong Univ Sci Technolog Med Sci. 2004;24(3):208-11.

PMID:
15315326

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