Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Elijah R. Behr"'
Publikováno v:
European Heart Journal
Artificial intelligence (AI) has given the electrocardiogram (ECG) and clinicians reading them super-human diagnostic abilities. Trained without hard-coded rules by finding often subclinical patterns in huge datasets, AI transforms the ECG, a ubiquit
Publikováno v:
European Heart Journal: Case Reports
Background Arrhythmogenic left ventricular cardiomyopathy (ALVC) is a rare form of arrhythmogenic cardiomyopathy characterized by fibrofatty replacement of left ventricular myocardium, malignant arrhythmia, and sudden cardiac death. The definition in
Autor:
Adam A. Witney, Tessa Homfray, Maite Tome, Elijah R. Behr, Nicholas Bunce, Belinda Gray, Michael Papadakis, Chris Miles, Paulo Bulleros, James S. Ware, Harshil Dhutia, Aneil Malhotra, Rajan Sharma, Bode Ensam, Zeph Fanton, Lisa J. Anderson, Stathis Papatheodorou, Mary N. Sheppard, Sanjay Sharma, Gherardo Finocchiaro
Publikováno v:
Europace
Aims Idiopathic left ventricular hypertrophy (LVH) is defined as LVH in the absence of myocyte disarray or secondary causes. It is unclear whether idiopathic LVH represents the phenotypic spectrum of hypertrophic cardiomyopathy (HCM) or whether it is
Autor:
Angeliki Asimaki, Joseph Westaby, David C Johnson, Maite Tome, Hamish MacLachlan, Elijah R. Behr, Gherardo Finocchiaro, Mary N. Sheppard, Joyee Basu, Carlos Bueno-Beti, Irina Chis Ster, Bode Ensam, Michael Papadakis, Khari A. Edwards, Sanjay Sharma, Chris Miles, Gemma Parry-Williams, Belinda Gray
BACKGROUND: Electrophysiological, imaging, and pathological studies have reported the presence of subtle structural abnormalities in hearts from patients with Brugada syndrome (BrS). However, data concerning disease involvement outside of the right v
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7062080bfc02c761105b40bc2df77234
https://openaccess.sgul.ac.uk/id/eprint/113763/1/j.jacc.2021.08.010.pdf
https://openaccess.sgul.ac.uk/id/eprint/113763/1/j.jacc.2021.08.010.pdf
Autor:
Giulio Conte, Kengo Kusano, David C Johnson, P. Delise, Shingo Maeda, Domenico Corrado, Belinda Gray, Leonardo Calò, Gi-Byoung Nam, Ruben Casado-Arroyo, Georgia Sarquella-Brugada, Aviram Hochstadt, Jean-Baptiste Gourraud, Christian Veltmann, Jacob Tfelt-Hansen, Silvia G Priori, Camilla H Jespersen, Ramon Brugada, Kenzo Hirao, Anat Milman, Carla Giustetto, Yuka Mizusawa, Jimmy Jm Juang, Giuseppe Allocca, Vincent Probst, Antoine Leenhardt, Pieter G. Postema, Bernard Belhassen, Andrea Mazzanti, Pedro Brugada, Elijah R. Behr, Elena Arbelo, Josep Brugada, T Kamakura, Antoine Andorin, Masahiko Takagi, Isabelle Denjoy, Yoshihide Takahashi, Fiorenzo Gaita, Zhengrong Huang, Arthur A.M. Wilde, Sung Hwan Kim, Takeshi Aiba, Gan-Xin Yan
Publikováno v:
Circulation. Genomic and precision medicine, 14(5). Lippincott Williams and Wilkins Ltd.
Milman, A, Behr, E R, Gray, B, Johnson, D C, Andorin, A, Hochstadt, A, Gourraud, J-B, Maeda, S, Takahashi, Y, Jm Juang, J, Kim, S-H, Kamakura, T, Aiba, T, Postema, P G, Mizusawa, Y, Denjoy, I, Giustetto, C, Conte, G, Huang, Z, Sarquella-Brugada, G, Mazzanti, A, Jespersen, C H, Arbelo, E, Brugada, R, Calo, L, Corrado, D, Casado-Arroyo, R, Allocca, G, Takagi, M, Delise, P, Brugada, J, Tfelt-Hansen, J, Priori, S G, Veltmann, C, Yan, G-X, Brugada, P, Gaita, F, Leenhardt, A, Wilde, A A M, Kusano, K F, Nam, G-B, Hirao, K, Probst, V & Belhassen, B 2021, ' Genotype-Phenotype Correlation of SCN5A Genotype in Patients With Brugada Syndrome and Arrhythmic Events : Insights From the SABRUS in 392 Probands ', Circulation. Genomic and precision medicine, vol. 14, no. 5, e003222 . https://doi.org/10.1161/CIRCGEN.120.003222
Circulation-Genomic and Precision Medicine
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
Milman, A, Behr, E R, Gray, B, Johnson, D C, Andorin, A, Hochstadt, A, Gourraud, J-B, Maeda, S, Takahashi, Y, Jm Juang, J, Kim, S-H, Kamakura, T, Aiba, T, Postema, P G, Mizusawa, Y, Denjoy, I, Giustetto, C, Conte, G, Huang, Z, Sarquella-Brugada, G, Mazzanti, A, Jespersen, C H, Arbelo, E, Brugada, R, Calo, L, Corrado, D, Casado-Arroyo, R, Allocca, G, Takagi, M, Delise, P, Brugada, J, Tfelt-Hansen, J, Priori, S G, Veltmann, C, Yan, G-X, Brugada, P, Gaita, F, Leenhardt, A, Wilde, A A M, Kusano, K F, Nam, G-B, Hirao, K, Probst, V & Belhassen, B 2021, ' Genotype-Phenotype Correlation of SCN5A Genotype in Patients With Brugada Syndrome and Arrhythmic Events : Insights From the SABRUS in 392 Probands ', Circulation. Genomic and precision medicine, vol. 14, no. 5, e003222 . https://doi.org/10.1161/CIRCGEN.120.003222
Circulation-Genomic and Precision Medicine
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
Background: Brugada syndrome (BrS) is associated with mutations in the cardiac sodium channel gene, SCN5A. However, genetic studies of patients with BrS with arrhythmic events have been limited. We sought to compare various clinical, ECG, and electro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4996f0a0777debaf7d4e6c5402d63c04
https://pure.amc.nl/en/publications/genotypephenotype-correlation-of-scn5a-genotype-in-patients-with-brugada-syndrome-and-arrhythmic-events(30208168-1225-4d88-9df0-8b320cc73dcd).html
https://pure.amc.nl/en/publications/genotypephenotype-correlation-of-scn5a-genotype-in-patients-with-brugada-syndrome-and-arrhythmic-events(30208168-1225-4d88-9df0-8b320cc73dcd).html
Autor:
Peter Lichtner, Thomas Meitinger, Wataru Shimizu, Alison Muir, F. Kyndt, Michael W.T. Tanck, Seiko Ohno, Martina Muggenthaler, Michael J. Ackerman, Vincent Probst, Stephen P. Page, Jean-Jacques Schott, Silvia Castelletti, Hariharan Raju, Jean-Baptiste Gourraud, Joseph Galvin, Taisuke Ishikawa, Eline A. Nannenberg, Dan M. Roden, Doris Škorić-Milosavljević, Kazuhiro Takahashi, Pascal P. McKeown, Federica Dagradi, Lia Crotti, Yanushi D. Wijeyeratne, Julien Barc, Yuka Mizusawa, Peter J. Schwartz, Michael Papadakis, Margherita Torchio, Sanjay Sharma, Velislav N. Batchvarov, Naomasa Makita, Richard Redon, Christian Veltmann, Elijah R. Behr, Takeshi Aiba, Martin Borggrefe, Rafik Tadros, Connie R. Bezzina, J. Martijn Bos, David J. Tester, Isabelle Denjoy, Minoru Horie, Arthur A.M. Wilde
Publikováno v:
Circ. Genom. Precis. Med. 13, 599-608 (2020)
Circulation: Genomic and Precision Medicine
Circulation: Genomic and Precision Medicine, American Heart Association, 2020, 13 (6), ⟨10.1161/CIRCGEN.120.002911⟩
Circulation: Genomic and Precision Medicine, 2020, 13 (6), ⟨10.1161/CIRCGEN.120.002911⟩
Circulation: Genomic and Precision Medicine, 599-608. Lippincott Williams and Wilkins Ltd.
STARTPAGE=599;ENDPAGE=608;ISSN=2574-8300;TITLE=Circulation: Genomic and Precision Medicine
Circulation. Genomic and Precision Medicine
Circulation: Genomic and Precision Medicine
Circulation: Genomic and Precision Medicine, American Heart Association, 2020, 13 (6), ⟨10.1161/CIRCGEN.120.002911⟩
Circulation: Genomic and Precision Medicine, 2020, 13 (6), ⟨10.1161/CIRCGEN.120.002911⟩
Circulation: Genomic and Precision Medicine, 599-608. Lippincott Williams and Wilkins Ltd.
STARTPAGE=599;ENDPAGE=608;ISSN=2574-8300;TITLE=Circulation: Genomic and Precision Medicine
Circulation. Genomic and Precision Medicine
Supplemental Digital Content is available in the text.
Background: Brugada syndrome (BrS) is characterized by the type 1 Brugada ECG pattern. Pathogenic rare variants in SCN5A (mutations) are identified in 20% of BrS families in whom incomplete
Background: Brugada syndrome (BrS) is characterized by the type 1 Brugada ECG pattern. Pathogenic rare variants in SCN5A (mutations) are identified in 20% of BrS families in whom incomplete
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf0dd4698c2a81d312e6f868f16dce14
https://openaccess.sgul.ac.uk/id/eprint/112608/1/CIRCGEN.120.002911.pdf
https://openaccess.sgul.ac.uk/id/eprint/112608/1/CIRCGEN.120.002911.pdf
Autor:
N Bunce, Andrew D'Silva, Zephryn Fanton, Gherardo Finocchiaro, Jessica Webb, Maria Teresa Tome Esteban, Sanjay Sharma, Gerry Carr-White, Lynne Millar, Michael Papadakis, Matthew Reed, Gabriel Sanchez-Fernandez, Aneil Malhotra, Ahmed Merghani, David Oxborough, Rajan Sharma, Harshil Dhutia, Elijah R. Behr, Jamie M. O’Driscoll
Publikováno v:
Heart (British Cardiac Society). 106(19)
The Authors’ reply We are grateful to Dr Stuart1 for his interest in our paper.2 We agree entirely that our dilated cardiomyopathy (DCM) cohort were indeed highly selected. Most individuals with DCM do not have the capacity to exercise intensively
Autor:
N Bunce, Zephryn Fanton, Matthew Reed, Gherardo Finocchiaro, Ahmed Merghani, Gabriel Sanchez-Fernandez, Michael Papadakis, Aneil Malhotra, Jamie M. O’Driscoll, Rajan Sharma, Harshil Dhutia, Maria Teresa Tome Esteban, David Oxborough, Andrew D'Silva, Gerry Carr-White, Elijah R. Behr, Lynne Millar, Sanjay Sharma, Jessica Webb
Publikováno v:
Heart (British Cardiac Society). 106(14)
ObjectiveDistinguishing early dilated cardiomyopathy (DCM) from physiological left ventricular (LV) dilatation with LV ejection fraction MethodsThirty-five asymptomatic active males with DCM, 25 male athletes in the ‘grey zone’ and 24 male athlet
Publikováno v:
Circulation. Arrhythmia and electrophysiology. 12(8)
Sudden cardiac death is defined as a death occurring usually within an hour of onset of symptoms, arising from an underlying cardiac disease. Sudden cardiac death is a complication of a number of cardiovascular diseases and is often unexpected. In in
Publikováno v:
Journal of the Royal Army Medical Corps. 161:253-258
Members of the Armed Forces may be exposed to drugs, or combinations of drugs, with the potential to prolong the QRS or QT intervals. The effect of this is to increase the likelihood of developing dangerous ventricular tachyarrhythmias, including ven