Results 221 to 230 of about 266,382 (322)

Exploring the mechanisms of sex-specific proarrhythmia in long QT syndrome through computational modeling. [PDF]

Am J Physiol Heart Circ Physiol
Doherty I, Shetty R, Ni H, Morotti S, Grandi E.   +4 more
europepmc   +1 more source

Classification and Reporting of Potentially Proarrhythmic Common Genetic Variation in Long QT Syndrome Genetic Testing

Circulation, 2018
J. Giudicessi, D. Roden, A. Wilde, M. Ackerman   +3 more
semanticscholar   +1 more source

Clinical, Electrical, and Mechanical Parameters in Potassium Channel-Mediated Congenital Long QT Syndrome. [PDF]

J Clin Med
Bileišienė N, Mikštienė V, Preikšaitienė E, Kažukauskienė I, Tarutytė G, Zakarkaitė D, Kramena R, Marinskis G, Aidietis A, Barysienė J.   +9 more
europepmc   +1 more source

Prevalence of the Congenital Long-QT Syndrome

Circulation, 2009
P. Schwartz, M. Stramba-Badiale, L. Crotti, M. Pedrazzini, A. Besana, G. Bosi, F. Gabbarini, K. Goulene, R. Insolia, S. Mannarino, F. Mosca, L. Nespoli, A. Rimini, E. Rosati, P. Salice, C. Spazzolini   +15 more
semanticscholar   +1 more source

Electrocardiographic Discrimination of Long QT Syndrome Genotypes: A Comparative Analysis and Machine Learning Approach. [PDF]

Sensors (Basel)
Srutova M, Kremen V, Lhotska L.
europepmc   +1 more source

Long QT Syndrome: LQT3 Variant Presenting in a Bradycardic Newborn. [PDF]

Cureus
Afonso C, Mendes DA, Queirós RV, Serra CM, Laranjo S.   +4 more
europepmc   +1 more source

Homozygous SCN5A Mutation in Long-QT Syndrome With Functional Two-to-One Atrioventricular Block [PDF]

, 2001
Jean‐Marc Lupoglazoff, T. Cheav, Ghayath Baroudi, Myriam Berthet, Isabelle Denjoy, B Cauchemez, Fabrice Extramiana, Mohamed Chahine, Pascale Guicheney   +8 more
openalex   +1 more source

Induced Pluripotent Stem Cells in Congenital Long QT Syndrome: Research Progress and Clinical Applications. [PDF]

Rev Cardiovasc Med
Li Q, Wang YF, Wang B, Lv TT, Zhang P.
europepmc   +1 more source

Homozygosity for a HERG potassium channel mutation causes a severe form of long QT syndrome: identification of an apparent founder mutation in the Finns

, 2000
Kirsi Piippo, Päivi Laitinen, Heikki Swan, Lauri Toivonen, Matti Viitasalo, Michael Pasternack, Kristian Paavonen, Hugh Chapman, Kenneth T. Wann, Eeva Hirvelä, Antti Sajantila, Kimmo Kontula   +11 more
openalex   +1 more source

Long-QT Syndrome-Associated Missense Mutations in the Pore Helix of the HERG Potassium Channel [PDF]

, 2001
Fu-De Huang, Jun Chen, Monica Lin, Mark T. Keating, Michael C. Sanguinetti   +4 more
openalex   +1 more source