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Items: 14


Long QT syndrome: how effective therapy in a single patient favorably influenced the long-term clinical course and genetic understanding of this hereditary disorder.

Lowengrub KM, Moss DR, Moss DA, Moss AJ.

Prog Cardiovasc Dis. 2015 Sep-Oct;58(2):221-6. doi: 10.1016/j.pcad.2015.08.002. Epub 2015 Aug 4.


Congenital and drug-induced long-QT syndrome: an update.

Wehrens XH, Doevendans PA.

Neth Heart J. 2004 Apr;12(4):165-172.


Oral contraceptive use and the risk of cardiac events in patients with long QT syndrome.

Abu-Zeitone A, Peterson DR, Polonsky B, McNitt S, Moss AJ.

Heart Rhythm. 2014 Jul;11(7):1170-5. doi: 10.1016/j.hrthm.2014.04.016. Epub 2014 Apr 13.


Cytoskeletal basis of ion channel function in cardiac muscle.

Vatta M, Faulkner G.

Future Cardiol. 2006 Jul;2(4):467-76. doi: 10.2217/14796678.2.4.467.


Analysis of genetic and non-genetic factors that affect the QTc interval in a Mongolian population: the GENDISCAN study.

Im SW, Lee MK, Lee HJ, Oh SI, Kim HL, Sung J, Cho SI, Seo JS, Kim JI.

Exp Mol Med. 2009 Nov 30;41(11):841-8. doi: 10.3858/emm.2009.41.11.090. Erratum in: Exp Mol Med. 2009 Dec 31;41(12):946.


Single-channel properties of IKs potassium channels.

Yang Y, Sigworth FJ.

J Gen Physiol. 1998 Dec;112(6):665-78. Erratum in: J Gen Physiol 1999 Mar;113(3):505.


Evidence of a long QT founder gene with varying phenotypic expression in South African families.

de Jager T, Corbett CH, Badenhorst JC, Brink PA, Corfield VA.

J Med Genet. 1996 Jul;33(7):567-73.


Evidence of genetic and phenotypic heterogeneity in the Romano-Ward syndrome.

Dean JC, Cross S, Jennings K.

J Med Genet. 1993 Nov;30(11):947-50.


Counselling pitfalls in Romano-Ward syndrome.

Dean JC, Cross S, Jennings K.

J Med Genet. 1993 Oct;30(10):886. No abstract available.


Molecular genetic aspects of the Romano-Ward long QT syndrome.

Towbin JA.

Tex Heart Inst J. 1994;21(1):42-7. Review.


Locus heterogeneity of autosomal dominant long QT syndrome.

Curran M, Atkinson D, Timothy K, Vincent GM, Moss AJ, Leppert M, Keating M.

J Clin Invest. 1993 Aug;92(2):799-803.


Analysis of HLA and disease susceptibility: chromosome 6 genes and sex influence long-QT phenotype.

Weitkamp LR, Moss AJ, Lewis RA, Hall WJ, MacCluer JW, Schwartz PJ, Locati EH, Tzivoni D, Vincent GM, Robinson JL, et al.

Am J Hum Genet. 1994 Dec;55(6):1230-41.


Familial dilated cardiomyopathy.

Mestroni L, Krajinovic M, Severini GM, Pinamonti B, Di Lenarda A, Giacca M, Falaschi A, Camerini F.

Br Heart J. 1994 Dec;72(6 Suppl):S35-41. Review. No abstract available.


Mapping of a gene for long QT syndrome to chromosome 4q25-27.

Schott JJ, Charpentier F, Peltier S, Foley P, Drouin E, Bouhour JB, Donnelly P, Vergnaud G, Bachner L, Moisan JP, et al.

Am J Hum Genet. 1995 Nov;57(5):1114-22.

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