Candidacy and long-term outcomes of subcutaneous implantable cardioverter-defibrillators in current practice in patients with hypertrophic cardiomyopathy

Authors: Rella, V., Maurizi, N., Bernardini, A., Brasca, F.M., Salerno, S., Meda, M., Mariani, D., Torchio, M., Ravaro, S., Cerea, P., Castelletti, S., Fumagalli, C., Conte, G., Auricchio, A., Girolami, F., Pieragnoli, P., Carrassa, G.M., Parati, G., Olivotto, I., Perego, G.B., Cecchi, F., Crotti, L.

Source: In International Journal of Cardiology 15 August 2024 409

Clinical risk factors associated with ventricular fibrillation during first ST-elevation myocardial infarction

Authors: Warming, PE, Glinge, C, Jabbari, R, Stampe, NK, Dusi, V, Tan, HL, Bezzina, CR, Crotti, L, De Ferrari, GM, Engstrom, T, Schwartz, PJ, Wilde, AAM, Tfelt-Hansen, J

Source: Europace. 24(Supplement 1)

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100165254661.0x000001&indx=1&recIds=ETOCvdc_100165254661.0x000001

Symbolic Analysis of Heart Period and QT Interval Variabilities in LQT1 Patients
Medical and biological engineering and computing; XIII Mediterranean MEDICON 2013

Authors: Bari, V., Bassani, T., Marchi, A., Girardengo, G., Calvillo, L., Cerutti, S., Brink, P.A., Crotti, L., Schwartz, P.J., Porta, A.

Source: IFMBE PROCEEDINGS. 41(1):531-534

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCCN085524615&indx=1&recIds=ETOCCN085524615

Elucidating arrhythmogenic mechanisms of long-QT syndrome CALM1-F142L mutation in patient-specific induced pluripotent stem cell-derived cardiomyocytes

Authors: Rocchetti, M., Sala, L., Dreizehnter, L., Crotti, L., Sinnecker, D., Mura, M., Pane, L. S., Altomare, C., Torre, E., Mostacciuolo, G.

Source: CARDIOVASCULAR RESEARCH. 113(5):531-541

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCRN384507303&indx=1&recIds=ETOCRN384507303

The genetics underlying acquired long QT syndrome: impact for genetic screening

Authors: Itoh, H., Crotti, L., Aiba, T., Spazzolini, C., Denjoy, I., Fressart, V. r., Hayashi, K., Nakajima, T., Ohno, S., Makiyama, T.

Source: EUROPEAN HEART JOURNAL. 37(18):1456-1464

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCRN377638734&indx=1&recIds=ETOCRN377638734

Brugada and Long QT Syndrome Are Two Different Diseases: True or False?
Cardiac arrhythmias

Authors: Priori, S. G., Crotti, L.

Source: CARDIAC ARRHYTHMIAS -INTERNATIONAL WORKSHOP-. :291-298

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCCN034185311&indx=1&recIds=ETOCCN034185311

Autonomic Control of Heart Rate and QT Interval Variability Influences Arrhythmic Risk in Long QT Syndrome Type 1

Authors: Porta, A., Girardengo, G., Bari, V., George, A. L., Brink, P. A., Goosen, A., Crotti, L., Schwartz, P. J.

Source: JOURNAL- AMERICAN COLLEGE OF CARDIOLOGY. 65(4):367-374

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCRN366331310&indx=1&recIds=ETOCRN366331310

AKAP9 Is a Genetic Modifier of Congenital Long-QT Syndrome Type 1

Authors: de Villiers, C.P., van der Merwe, L., Crotti, L., Goosen, A., George, A.L., Schwartz, P.J., Brink, P.A., Moolman-Smook, J.C., Corfield, V.A.

Source: CIRCULATION CARDIOVASCULAR GENETICS. 7(5):599-606

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCRN361887916&indx=1&recIds=ETOCRN361887916

Novel Calmodulin Mutations Associated With Congenital Arrhythmia Susceptibility

Authors: Makita, N., Yagihara, N., Crotti, L., Johnson, C.N., Beckmann, B.-M., Roh, M.S., Shigemizu, D., Lichtner, P., Ishikawa, T., Aiba, T.

Source: CIRCULATION CARDIOVASCULAR GENETICS. 7(4):466-474

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCRN359951909&indx=1&recIds=ETOCRN359951909

Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization

Authors: Arking, D. E., Pulit, S. L., Crotti, L., van der Harst, P., Munroe, P. B., Koopmann, T. T., Sotoodehnia, N., Rossin, E. J., Morley, M., Wang, X.

Source: NATURE GENETICS. 46(8):826-836

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCRN357029234&indx=1&recIds=ETOCRN357029234

A comprehensive electrocardiographic, molecular, and echocardiographic study of Brugada syndrome: Validation of the 2013 diagnostic criteria

Authors: Savastano, S., Rordorf, R., Vicentini, A., Petracci, B., Taravelli, E., Castelletti, S., D'Errico, A., Torchio, M., Dossena, C., Novara, P., Dagradi, F., Landolina, M., Spazzolini, C., Crotti, L., Schwartz, P. J.

Source: HEART RHYTHM. 11(7):1176-1183

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCRN354502286&indx=1&recIds=ETOCRN354502286

Propranolol prevents life-threatening arrhythmias in LQT3 transgenic mice: Implications for the clinical management of LQT3 patients

Authors: Calvillo, L., Spazzolini, C., Vullo, E., Insolia, R., Crotti, L., Schwartz, P. J.

Source: HEART RHYTHM. 11(1):126-132

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCRN344964073&indx=1&recIds=ETOCRN344964073

FGF12 is a candidate Brugada syndrome locus
Focus Issue: Devices

Authors: Hennessey, J. A., Marcou, C. A., Wang, C., Wei, E. Q., Tester, D. J., Torchio, M., Dagradi, F., Crotti, L., Schwartz, P. J., Ackerman, M. J., Pitt, G. S.

Source: HEART RHYTHM. 10(12):1886-1894

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCRN344021154&indx=1&recIds=ETOCRN344021154

Identification of a KCNQ1 Polymorphism Acting as a Protective Modifier Against Arrhythmic Risk in Long-QT Syndrome

Authors: Duchatelet, S., Crotti, L., Peat, R.A., Denjoy, I., Itoh, H., Berthet, M., Ohno, S., Fressart, V., Monti, M.C., Crocamo, C.

Source: CIRCULATION CARDIOVASCULAR GENETICS. 6(4):354-361

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCRN342199561&indx=1&recIds=ETOCRN342199561

Calmodulin Mutations Associated With Recurrent Cardiac Arrest in Infants

Authors: Crotti, L., Johnson, C.N., Graf, E., De Ferrari, G.M., Cuneo, B.F., Ovadia, M., Papagiannis, J., Feldkamp, M.D., Rathi, S.G., Kunic, J.D.

Source: CIRCULATION. 127(9):1009-1017

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCRN341159932&indx=1&recIds=ETOCRN341159932

Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

Authors: Bezzina, C. R., Barc, J., Mizusawa, Y., Remme, C. A., Gourraud, J. B., Simonet, F., Verkerk, A. O., Schwartz, P. J., Crotti, L., Dagradi, F.

Source: NATURE GENETICS. 45(9):1044-1049

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCRN338094009&indx=1&recIds=ETOCRN338094009

Long QT Syndrome-Associated Mutations in Intrauterine Fetal Death

Authors: Crotti, L., Tester, D.J., White, W.M., Bartos, D.C., Insolia, R., Besana, A., Kunic, J.D., Will, M.L., Velasco, E.J., Bair, J.J.

Source: JOURNAL- AMERICAN MEDICAL ASSOCIATION. 309(14):1473-1482

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCRN330565511&indx=1&recIds=ETOCRN330565511

Clinical conditions associated with abnormal QT interval: clinical implications

Authors: Crotti, L., Dossena, C., Mastantuono, E., Dagradi, F., Schwartz, P.J.

Source: GIORNALE ITALIANO DI CARDIOLOGIA -NEW SERIES-. 14(1):55-65

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCRN326865599&indx=1&recIds=ETOCRN326865599

Torsades de pointes following acute myocardial infarction: Evidence for a deadly link with a common genetic variant

Authors: Crotti, L., Hu, D., Barajas-Martinez, H., De Ferrari, G.M., Oliva, A., Insolia, R., Pollevick, G.D., Dagradi, F., Guerchicoff, A., Greco, F.

Source: HEART RHYTHM. 9(7):1104-1112

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCRN327029769&indx=1&recIds=ETOCRN327029769

A Novel Disease Gene for Brugada Syndrome: Sarcolemmal Membrane-Associated Protein Gene Mutations Impair Intracellular Trafficking of hNav1.5

Authors: Ishikawa, T., Sato, A., Marcou, C.A., Tester, D.J., Ackerman, M.J., Crotti, L., Schwartz, P.J., On, Y.K., Park, J.-E., Nakamura, K.

Source: CIRCULATION ARRHYTHMIA AND ELECTROPHYSIOLOGY. 5(6):1098-1107

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCRN325157134&indx=1&recIds=ETOCRN325157134