Sacubitril/valsartan eligibility and outcomes in the ESC‐EORP‐HFA Heart Failure Long‐Term Registry: bridging between European Medicines Agency/Food and Drug Administration label, t... von Ruschitzka, Frank, Ablasser, K., Brandner, K., Gstrein, S., Hegarova, M., Noamany, M., Farag, N., Aziz, R., Nasr, G., Ashmawy, M., Meneveau, N., Seronde, M‐F., Jondeau, G., Thebault, C., Codjia, R., Tousoulis, D., Kotrogiannis, I., Kapelios, C., Saloustros, I., Evangelou, S., Papadopoulou, A., Kosztin, A., Penco, M., Correale, M., Agostoni, P., Salvioni, E., Modena, M.G., Bandino, S., Di Ruocco, M.V., Licata, G., Giambanco, S., Chirco, P.R., Teresi, G., Priori, S.G., Cattaneo, S., Gualco, A., Pagliaro, M., Romeo, F., Ferraiuolo, F., Frea, S., Merlo, M., Sinagra, G., Daneluzzi, C., Gabryel, J., Bala, A., Flis, P., Grajek, S., Straburzynska‐Migaj, E., Zysko, D., Mamcarz, A., Zielinski, T., Rywik, T., Sobieszczanska‐Malek, M., Balsam, P., Gil, K., Skrobowski, A., Ponikowski, P., Prokop‐Lewicka, G., Kleinrok, A., Castro, A., Brito, D., Araujo, I., Silva‐Cardoso, J., Marta, L., Severino, D., Popescu, R., Craiu, E., Christodorescu, R., Suzic Lazic, J., Atanaskovic, V., Ilic, S., Kecojevic, S., Stojiljkovic, J., Goncalvesova, E., Glavic, T., Cencic, V., Bartolic, A., Slemenik Pusnik, C., Leskovar, B., Salmeron Martinez, F.M., Bayes‐Genis, A., Mendez, A., Roig, E., Leon, V., Gonzalez‐Costello, J., Laynez Cerdena, I., Segovia Cubero, J., Sayago, I., Gonzalez‐Segovia, A., Ruiz Cano, M.J., Sahuquillo, A., Martinez‐Abellan, R., Perez‐Silvestre, J., Ridocci‐Soriano, F., Pellicer‐Cabo, A., Sanz Julve, M., Aured‐Guallar, C., Portoles‐Ocampo, A., Olsson, L., Temizhan, A.

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Severe Arrhythmia Disorder Caused by Cardiac L-Type Calcium Channel Mutations von Splawski, Igor, Timothy, Katherine W., Decher, Niels, Kumar, Pradeep, Sachse, Frank B., Beggs, Alan H., Sanguinetti, Michael C., Keating, Mark T.

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A Cardiac Arrhythmia Syndrome Caused by Loss of Ankyrin-B Function von Mohler, Peter J., Splawski, Igor, Napolitano, Carlo, Bottelli, Georgia, Sharpe, Leah, Timothy, Katherine, Priori, Silvia G., Keating, Mark T., Bennett, Vann, Latorre, Ramon

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Variant of SCN5A Sodium Channel Implicated in Risk of Cardiac Arrhythmia von Splawski, Igor, Timothy, Katherine W., Tateyama, Michihiro, Clancy, Colleen E., Malhotra, Alka, Beggs, Alan H., Cappuccio, Francesco P., Sagnella, Giuseppe A., Kass, Robert S., Keating, Mark T.

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Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias von Wang, Q, Curran, M.E, Splawski, I, Burn, T.C, Millholland, J.M, VanRaay, T.J, Shen, J, Timothy, K.W, Vincent, G.M, de Jager, T, Schwartz, P.J, Towbin, J.A, Moss, A.J, Atkinson, D.L, Landes, G.M, Connors, T.D, Keating, M.T

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Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism von Splawski, Igor, Timothy, Katherine W, Sharpe, Leah M, Decher, Niels, Kumar, Pradeep, Bloise, Raffaella, Napolitano, Carlo, Schwartz, Peter J, Joseph, Robert M, Condouris, Karen, Tager-Flusberg, Helen, Priori, Silvia G, Sanguinetti, Michael C, Keating, Mark T

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Take-Home Naloxone Program Implementation: Lessons Learned From Seven Chicago-Area Hospitals von Eswaran, Vidya, Allen, Katherine C., Bottari, Diana C., Splawski, Jennifer A., Bains, Sukheer, Aks, Steven E., Swoboda, Henry D., Moore, P. Quincy, Tran, Tran H., Salisbury-Afshar, Elizabeth, Lank, Patrick M., McCarthy, Danielle M., Kim, Howard S.

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Spectrum of mutations in long-QT syndrome genes : KVLQT1, HERG, SCN5A, KCNE1, and KCNE2 von SPLAWSKI, I, JIAXIANG SHEN, KEATING, M. T, TIMOTHY, K. W, LEHMANN, M. H, PRIORI, S, ROBINSON, J. L, MOSS, A. J, SCHWARTZ, P. J, TOWBIN, J. A, VINCENT, G. M

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A Survey of Staff Perceptions of an Emergency Medicine Pharmacist Program in a Community Hospital: A Brief Report von Splawski, Jennifer, PharmD, Horner, Deanna, PharmD, Tao, Kevin, MD

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Spectrum and prevalence of cardiac sodium channel variants among black, white, Asian, and Hispanic individuals: Implications for arrhythmogenic susceptibility and Brugada/long QT s... von Ackerman, Michael J., Splawski, Igor, Makielski, Jonathan C., Tester, David J., Will, Melissa L., Timothy, Katherine W., Keating, Mark T., Jones, Gregg, Chadha, Monica, Burrow, Christopher R., Stephens, J. Claiborne, Xu, Chuanbo, Judson, Richard, Curran, Mark E.

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A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome von Curran, Mark E, Splawski, Igor, Timothy, Katherine W, Vincen, G.Michael, Green, Eric D, Keating, Mark T

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Compound mutations: A common cause of severe long-Qt syndrome von WESTENSKOW, Peter, SPLAWSKI, Igor, TIMOTHY, Katherine W, KEATING, Mark T, SANGUINETTI, Michael C

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Long QT Syndrome-associated Mutations in the Per-Arnt-Sim (PAS) Domain of HERG Potassium Channels Accelerate Channel Deactivation von Chen, J, Zou, A, Splawski, I, Keating, M T, Sanguinetti, M C

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MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia von Abbott, G W, Sesti, F, Splawski, I, Buck, M E, Lehmann, M H, Timothy, K W, Keating, M T, Goldstein, S A

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Characterization of an Early-Onset, Autosomal Recessive, Progressive Retinal Degeneration in Bengal Cats von Ofri, Ron, Reilly, Christopher M, Maggs, David J, Fitzgerald, Paul G, Shilo-Benjamini, Yael, Good, Kathryn L, Grahn, Robert A, Splawski, Danielle D, Lyons, Leslie A

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SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome von Wang, Qing, Shen, Jiaxiang, Splawski, Igor, Atkinson, Donald, Li, Zhizhong, Robinson, Jennifer L, Moss, Arthur J, Towbin, Jeffrey A, Keating, Mark T

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Inflammatory disease in HLA-B27 transgenic rats von Taugor, Joel D., Maika, Shanna D., Satumtira, Nimman, Dorris, Martha L., McLean, Ian Lochlan, Yanagisawa, Hiromi, Sayad, Alain, Stagg, Andrew J., Fox, Graham M., Le O'Brein, Anne, Rehman, Muhammad, Zhou, Ming, Weiner, Allison L., Splawski, Judy B., Richardson, James A., Hammer, Robert E.

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Genomic structure of three long QT syndrome genes : KVLQT1, HERG, and KCNE1 von SPLAWSKI, I, JIAXIANG SHEN, TIMOTHY, K. W, VINCENT, G. M, LEHMANN, M. H, KEATING, M. T

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Spectrum of ST-T-wave patterns and repolarization parameters in congenital long-QT syndrome : ECG findings identify genotypes von LI ZHANG, TIMOTHY, Katherine W, YANOWITZ, Frank, BENHORIN, Jesaia, MOSS, Arthur J, SCHWARTZ, Peter J, ROBINSON, Jennifer L, QING WANG, ZAREBA, Wojciech, KEATING, Mark T, TOWBIN, Jeffrey A, NAPOLITANO, Carlo, VINCENT, G. Michael, MEDINA, Aharon, LEHMANN, Michael H, FOX, Jolene, GIULI, Lisa C, JIAXIANG SHEN, SPLAWSKI, Igor, PRIORI, Silvia G, COMPTON, Steven J

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Molecular Basis of the Long-QT Syndrome Associated with Deafness von Splawski, Igor, Timothy, Katherine W, Vincent, G. Michael, Atkinson, Donald L, Keating, Mark T

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