Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Elijah R. Behr"'
Autor:
Charlotte Glinge, Sára Rossetti, Louise Bruun Oestergaard, Niels Kjær Stampe, Thomas Hadberg Lynge, Regitze Skals, Bo Gregers Winkel, Elisabeth M. Lodder, Connie R. Bezzina, Gunnar Gislason, Jytte Banner, Elijah R. Behr, Christian Torp-Pedersen, Reza Jabbari, Jacob Tfelt-Hansen
Publikováno v:
Glinge, C, Rossetti, S, Oestergaard, L B, Stampe, N K, Lynge, T H, Skals, R, Winkel, B G, Lodder, E M, Bezzina, C R, Gislason, G, Banner, J, Behr, E R, Torp-Pedersen, C, Jabbari, R & Tfelt-Hansen, J 2023, ' Risk of Sudden Infant Death Syndrome among Siblings of Children Who Died of Sudden Infant Death Syndrome in Denmark ', JAMA network open, vol. 6, no. 1, E2252724 . https://doi.org/10.1001/jamanetworkopen.2022.52724
Glinge, C, Rossetti, S, Oestergaard, L B, Stampe, N K, Lynge, T H, Skals, R, Winkel, B G, Lodder, E M, Bezzina, C R, Gislason, G, Banner, J, Behr, E R, Torp-Pedersen, C, Jabbari, R & Tfelt-Hansen, J 2023, ' Risk of Sudden Infant Death Syndrome Among Siblings of Children Who Died of Sudden Infant Death Syndrome in Denmark ', JAMA Network Open, vol. 6, no. 1, e2252724, pp. E2252724 . https://doi.org/10.1001/jamanetworkopen.2022.52724
JAMA network open, 6(1). American Medical Association
Glinge, C, Rossetti, S, Oestergaard, L B, Stampe, N K, Lynge, T H, Skals, R, Winkel, B G, Lodder, E M, Bezzina, C R, Gislason, G, Banner, J, Behr, E R, Torp-Pedersen, C, Jabbari, R & Tfelt-Hansen, J 2023, ' Risk of Sudden Infant Death Syndrome Among Siblings of Children Who Died of Sudden Infant Death Syndrome in Denmark ', JAMA Network Open, vol. 6, no. 1, e2252724, pp. E2252724 . https://doi.org/10.1001/jamanetworkopen.2022.52724
JAMA network open, 6(1). American Medical Association
ImportanceSudden infant death syndrome (SIDS) remains a leading cause of death during the first year of life. The etiology of SIDS is complex and remains largely unknown.ObjectiveTo evaluate whether siblings of children who died of SIDS have a higher
Autor:
Puck J. Peltenburg, Dania Kallas, Johan M. Bos, Krystien V.V. Lieve, Sonia Franciosi, Thomas M. Roston, Isabelle Denjoy, Katrina B. Sorensen, Seiko Ohno, Ferran Roses-Noguer, Takeshi Aiba, Alice Maltret, Martin J. LaPage, Joseph Atallah, John R. Giudicessi, Sally-Ann B. Clur, Nico A. Blom, Michael Tanck, Fabrice Extramiana, Koichi Kato, Julien Barc, Martin Borggrefe, Elijah R. Behr, Georgia Sarquella-Brugada, Jacob Tfelt-Hansen, Esther Zorio, Heikki Swan, Janneke A.E. Kammeraad, Andrew D. Krahn, Andrew Davis, Frederic Sacher, Peter J. Schwartz, Jason D. Roberts, Jonathan R. Skinner, Maarten P. van den Berg, Prince J. Kannankeril, Fabrizio Drago, Tomas Robyns, Kristina Haugaa, Terezia Tavacova, Christopher Semsarian, Jan Till, Vincent Probst, Ramon Brugada, Wataru Shimizu, Minoru Horie, Antoine Leenhardt, Michael J. Ackerman, Shubhayan Sanatani, Christian van der Werf, Arthur A.M. Wilde
Publikováno v:
Circulation, 145(5), 333-344. Lippincott Williams & Wilkins
Circulation, 145(5), 333-344. Lippincott Williams and Wilkins
Peltenburg, P J, Kallas, D, Bos, J M, Lieve, K V V, Franciosi, S, Roston, T M, Denjoy, I, Sorensen, K B, Ohno, S, Roses-Noguer, F, Aiba, T, Maltret, A, Lapage, M J, Atallah, J, Giudicessi, J R, Clur, S-A B, Blom, N A, Tanck, M, Extramiana, F, Kato, K, Barc, J, Borggrefe, M, Behr, E R, Sarquella-Brugada, G, Tfelt-Hansen, J, Zorio, E, Swan, H, Kammeraad, J A E, Krahn, A D, Davis, A, Sacher, F, Schwartz, P J, Roberts, J D, Skinner, J R, van den Berg, M P, Kannankeril, P J, Drago, F, Robyns, T, Haugaa, K, Tavacova, T, Semsarian, C, Till, J, Probst, V, Brugada, R, Shimizu, W, Horie, M, Leenhardt, A, Ackerman, M J, Sanatani, S, van der Werf, C & Wilde, A A M 2022, ' An International Multicenter Cohort Study on β-Blockers for the Treatment of Symptomatic Children With Catecholaminergic Polymorphic Ventricular Tachycardia ', Circulation, vol. 145, no. 5, pp. 333-344 . https://doi.org/10.1161/CIRCULATIONAHA.121.056018
Circulation, 145(5), 333-344. LIPPINCOTT WILLIAMS & WILKINS
Circulation
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
Circulation, 145(5), 333-344. Lippincott Williams and Wilkins
Peltenburg, P J, Kallas, D, Bos, J M, Lieve, K V V, Franciosi, S, Roston, T M, Denjoy, I, Sorensen, K B, Ohno, S, Roses-Noguer, F, Aiba, T, Maltret, A, Lapage, M J, Atallah, J, Giudicessi, J R, Clur, S-A B, Blom, N A, Tanck, M, Extramiana, F, Kato, K, Barc, J, Borggrefe, M, Behr, E R, Sarquella-Brugada, G, Tfelt-Hansen, J, Zorio, E, Swan, H, Kammeraad, J A E, Krahn, A D, Davis, A, Sacher, F, Schwartz, P J, Roberts, J D, Skinner, J R, van den Berg, M P, Kannankeril, P J, Drago, F, Robyns, T, Haugaa, K, Tavacova, T, Semsarian, C, Till, J, Probst, V, Brugada, R, Shimizu, W, Horie, M, Leenhardt, A, Ackerman, M J, Sanatani, S, van der Werf, C & Wilde, A A M 2022, ' An International Multicenter Cohort Study on β-Blockers for the Treatment of Symptomatic Children With Catecholaminergic Polymorphic Ventricular Tachycardia ', Circulation, vol. 145, no. 5, pp. 333-344 . https://doi.org/10.1161/CIRCULATIONAHA.121.056018
Circulation, 145(5), 333-344. LIPPINCOTT WILLIAMS & WILKINS
Circulation
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
Background: Symptomatic children with catecholaminergic polymorphic ventricular tachycardia (CPVT) are at risk for recurrent arrhythmic events. β-Blockers decrease this risk, but studies comparing individual β-blockers in sizeable cohorts are lacki
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9763d1251c233799ab62ab359429a22b
https://openaccess.sgul.ac.uk/id/eprint/113944/1/CIRCULATIONAHA.121.056018.pdf
https://openaccess.sgul.ac.uk/id/eprint/113944/1/CIRCULATIONAHA.121.056018.pdf
Autor:
Keerthi Jaliparthy, Aiswarya Rajendran, R. Ross Reichard, Erik K. St. Louis, Mariha Khan, Michael J. Ackerman, Ahmed U. Fayyaz, Aradhana Sahoo, Elson L. So, David J. Tester, Virend K. Somers, William D. Edwards, Elijah R. Behr, Jennifer A. Knight, Michael A. Simpson, Nadeem Khan, C. Anwar A. Chahal, Dongmei Lu
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 10, Iss 23 (2021)
Background Sudden cardiac arrest is the leading mode of death in the United States. Epilepsy affects 1% of Americans; yet epidemiological data show a prevalence of 4% in cases of sudden cardiac arrest. Sudden unexpected death in epilepsy (SUDEP) may
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cfda18e6378a499946f6129983441d1f
https://openaccess.sgul.ac.uk/id/eprint/113892/1/JAHA.121.021170.pdf
https://openaccess.sgul.ac.uk/id/eprint/113892/1/JAHA.121.021170.pdf
Autor:
Christopher Semsarian, Daniel J. Clemens, Steven M. Dotzler, Richard D. Bagnall, Belinda Gray, Elijah R. Behr, Emma Matthews, David J. Tester, John R. Giudicessi, Michael J. Ackerman
Publikováno v:
Circulation: Genomic and Precision Medicine. 13
Background: Triadin knockout syndrome (TKOS) is a potentially lethal arrhythmia disorder caused by recessively inherited null variants in TRDN -encoded cardiac triadin. Despite its malignant phenotype, the prevalence of TKOS in sudden infant death sy
Autor:
Shingo Maeda, Yoav Michowitz, Yuka Mizusawa, Elijah R. Behr, Gan-Xin Yan, Georgia Sarquella-Brugada, Carlo Napolitano, Domenico Corrado, Tsukasa Kamakura, Zhengrong Huang, Antoine Leenhardt, Elena Arbelo, Ramon Brugada, Kengo Kusano, Carla Giustetto, Eran Leshem, Pieter G. Postema, Bernard Belhassen, Silvia G. Priori, Yoshihide Takahashi, Michael Rahkovich, Antoine Andorin, Kenzo Hirao, Jean-Baptiste Gourraud, Arthur A.M. Wilde, Christian Veltmann, Yanushi D. Wijeyeratne, Anat Milman, Pietro Delise, Ruben Casado-Arroyo, Jacob Tfelt-Hansen, Fiorenzo Gaita, Gi-Byoung Nam, Aviram Hochstadt, Vincent Probst, Leonardo Calo, Giulio Conte, Pedro Brugada, Takeshi Aiba, Jimmy J.M. Juang, Josep Brugada, Frederic Sacher, Jean Champagne, Philippe Mabo, Isabelle Denjoy, Sung Hwan Kim, Masahiko Takagi
Publikováno v:
Heart Rhythm
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Heart rhythm, 15(9), 1394-1401. Elsevier
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Heart rhythm, 15(9), 1394-1401. Elsevier
BACKGROUND: The literature on fever-related arrhythmic events (AEs) in Brugada syndrome (BrS) is currently limited to few case reports and small series. OBJECTIVE: The present study aimed to describe the characteristics of fever-related AE in a large
Autor:
Michael Christiansen, Elijah R. Behr, Jacob Tfelt-Hansen, Bo Gregers Winkel, Xinzhong Li, Steve Jeffery, Donald R. Love, Paula L. Hedley, Shibu John, Hariharan Raju, James S. Ware, Jonathan R. Skinner, Christian van der Werf, Gavin Arno, Marta C. Cohen, Arthur A. M. Wilde, Mary N. Sheppard, Sanjay Sharma
Publikováno v:
BMC cardiovascular disorders, 19(1):174. BioMed Central
Raju, H, Ware, J S, Skinner, J R, Hedley, P L, Arno, G, Love, D R, van der Werf, C, Tfelt-Hansen, J, Winkel, B G, Cohen, M C, Li, X, John, S, Sharma, S, Jeffery, S, Wilde, A A M, Christiansen, M, Sheppard, M N & Behr, E R 2019, ' Next-generation sequencing using microfluidic PCR enrichment for molecular autopsy ', BMC Cardiovascular Disorders, vol. 19, no. 1, 174 . https://doi.org/10.1186/s12872-019-1154-8
BMC Cardiovascular Disorders, Vol 19, Iss 1, Pp 1-10 (2019)
BMC Cardiovascular Disorders
Raju, H, Ware, J S, Skinner, J R, Hedley, P L, Arno, G, Love, D R, van der Werf, C, Tfelt-Hansen, J, Winkel, B G, Cohen, M C, Li, X, John, S, Sharma, S, Jeffery, S, Wilde, A A M, Christiansen, M, Sheppard, M N & Behr, E R 2019, ' Next-generation sequencing using microfluidic PCR enrichment for molecular autopsy ', BMC Cardiovascular Disorders, vol. 19, no. 1, 174 . https://doi.org/10.1186/s12872-019-1154-8
BMC Cardiovascular Disorders, Vol 19, Iss 1, Pp 1-10 (2019)
BMC Cardiovascular Disorders
Background We aimed to determine the mutation yield and clinical applicability of “molecular autopsy” following sudden arrhythmic death syndrome (SADS) by validating and utilizing low-cost high-throughput technologies: Fluidigm Access Array PCR-e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::761e2ad500e58a109bde74b4267115f4
https://pure.amc.nl/en/publications/nextgeneration-sequencing-using-microfluidic-pcr-enrichment-for-molecular-autopsy(a325145f-7305-4578-935b-7a75924b17c3).html
https://pure.amc.nl/en/publications/nextgeneration-sequencing-using-microfluidic-pcr-enrichment-for-molecular-autopsy(a325145f-7305-4578-935b-7a75924b17c3).html
Autor:
Elijah R. Behr, Iona Jeffrey, Belinda Gray, Margaret J. Evans, David J. Tester, Leonie C.H. Wong, Michael A. Simpson, Amie Jaye, Peter J. Fleming, Jared M. Evans, Pritha Chanana, Jacob Tfelt-Hansen, Michael J. Ackerman, Marta C. Cohen
Publikováno v:
Tester, D J, Wong, L C H, Chanana, P, Gray, B, Jaye, A, Evans, J M, Evans, M, Fleming, P, Jeffrey, I, Cohen, M, Tfelt-Hansen, J, Simpson, M A, Behr, E R & Ackerman, M J 2018, ' Exome-Wide Rare Variant Analyses in Sudden Infant Death Syndrome ', Journal of Pediatrics, vol. 203, pp. 423-428.e11 . https://doi.org/10.1016/j.jpeds.2018.08.011
Objective: To determine whether a monogenic basis explains sudden infant death syndrome (SIDS) using an exome-wide focus. Study design: A cohort of 427 unrelated cases of SIDS (257 male; average age = 2.7 ± 1.9 months) underwent whole-exome sequenci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30a7a27384a48e90ab6d3495a7042765
Autor:
Tsukasa Kamakura, Shingo Maeda, Leonardo Calo, Zhengrong Huang, Kenzo Hirao, Elena Arbelo, Arthur A.M. Wilde, Antoine Andorin, Domenico Corrado, Sung Hwan Kim, Yanushi D. Wijeyeratne, Yoav Michowitz, Christian Veltmann, Gi-Byoung Nam, Jean Champagne, Giulio Conte, Anat Milman, Jacob Tfelt-Hansen, Philippe Mabo, Takeshi Aiba, Michael Rahkovich, Carlo Napolitano, Pietro Delise, Pedro Brugada, Carla Giustetto, Silvia G. Priori, Fiorenzo Gaita, Antoine Leenhardt, Aviram Hochstadt, Vincent Probst, Jimmy J.M. Juang, Gan-Xin Yan, Jean-Baptiste Gourraud, Kengo Kusano, Georgia Sarquella-Brugada, Yuka Mizusawa, Isabelle Denjoy, Josep Brugada, Masahiko Takagi, Frederic Sacher, Pieter G. Postema, Bernard Belhassen, Ruben Casado-Arroyo, Elijah R. Behr, Ramon Brugada, Yoshihide Takahashi, Eran Leshem
Publikováno v:
Heart Rhythm
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
Heart rhythm, 15(10), 1457-1465. Elsevier
Heart rhythm, 15 (10
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
Heart rhythm, 15(10), 1457-1465. Elsevier
Heart rhythm, 15 (10
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
Background: There is limited information on gender differences in patients with Brugada syndrome (BrS) who experienced arrhythmic events (AEs). Objective: The purpose of this study was to compare clinical, electrocardiographic (ECG), electrophysiolog
Autor:
Takeshi Aiba, Raymond W. Sy, Jodie Ingles, Belinda Gray, Christopher Semsarian, Vincent Probst, Can Hasdemir, Mary N. Sheppard, Elijah R. Behr, Naomasa Makita, Arthur A.M. Wilde, Ruth Newbury-Ecob
Publikováno v:
Heart rhythm, 15(7), 1051-1057. Elsevier
WOS: 000436479200017
PubMed ID: 29758173
BACKGROUND There is limited evidence that Brugada Syndrome (BrS) is due to SCN1B variants (BrS5). This gene may be inappropriately included in routine genetic testing panels for BrS or Sudden Arrhyth
PubMed ID: 29758173
BACKGROUND There is limited evidence that Brugada Syndrome (BrS) is due to SCN1B variants (BrS5). This gene may be inappropriately included in routine genetic testing panels for BrS or Sudden Arrhyth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b709120a068efe15f0d5a529e8e0e940
https://hdl.handle.net/11454/30266
https://hdl.handle.net/11454/30266
Autor:
Michael J. Ackerman, Sonia Franciosi, Carla Spazzolini, Peter J. Schwartz, Laura Zahavich, Annika Winbo, Anna Joong, Hervé Le Marec, Arja S. Vink, Andrew D. Krahn, Isabelle Denjoy, Mangesh Jadhav, Béatrice Guyomarc’h-Delasalle, Virginie Beauséjour-Ladouceur, Johan M Bos, Nico A. Blom, Alban-Elouen Baruteau, Matthias Lachaud, Claudine Rieubland, Jean Marc Lupoglazoff, Minoru Horie, Yanushi D. Wijeyeratne, Peter C. Ruben, Mena Abdelsayed, Jonathan R. Skinner, Elijah R. Behr, George F. Van Hare, Dominic Abrams, Takeshi Aiba, Jean-Baptiste Gourraud, Arthur A.M. Wilde, Junichi Ozawa, Tak-cheung Yung, Wataru Shimizu, Jacob Tfelt-Hansen, Leonardo Liberman, Lia Crotti, Sit Yee Kwok, Anne M. Dubin, David J. Tester, Shubhayan Sanatani, Vincent Probst, Juan Pablo Kaski, Andrew M. Davis, Federica Dagradi, Elizabeth A. Stephenson, Véronique Fressart, Boris Rudic, Leonie C.H. Wong, F. Kyndt, Jean-Jacques Schott
Publikováno v:
Baruteau, Alban-Elouen; Kyndt, Florence; Behr, Elijah R; Vink, Arja S; Lachaud, Matthias; Joong, Anna; Schott, Jean-Jacques; Horie, Minoru; Denjoy, Isabelle; Crotti, Lia; Shimizu, Wataru; Bos, Johan M; Stephenson, Elizabeth A; Wong, Leonie; Abrams, Dominic J; Davis, Andrew M; Winbo, Annika; Dubin, Anne M; Sanatani, Shubhayan; Liberman, Leonardo; ... (2018). SCN5A mutations in 442 neonates and children: genotype-phenotype correlation and identification of higher-risk subgroups. European Heart Journal, 39(31), pp. 2879-2887. Oxford University Press 10.1093/eurheartj/ehy412
European heart journal, 39(31), 2879-2887. Oxford University Press
European heart journal, 39(31), 2879-2887. Oxford University Press
Aims To clarify the clinical characteristics and outcomes of children with SCN5A-mediated disease and to improve their risk stratification. Methods and results A multicentre, international, retrospective cohort study was conducted in 25 tertiary hosp