Zobrazeno 1 - 10
of 44
pro vyhledávání: '"James S. Ware"'
Autor:
Inga Voges, Amrit Lota, Resham Baruah, Paul J.R. Barton, James S. Ware, John Gregson, Sanjay K Prasad, Nicola Whiffin, Brian P Halliday, Julian W.E. Jarman, Dudley J. Pennell, Angharad M. Roberts, Michael P. Frenneaux, A. John Baksi, Rachel Buchan, Upasana Tayal, Stuart A. Cook, John G.F. Cleland
Publikováno v:
Heart. 108:619-625
ObjectiveThe effect of moderate excess alcohol consumption is widely debated and has not been well defined in dilated cardiomyopathy (DCM). There is need for a greater evidence base to help advise patients. We sought to evaluate the effect of moderat
Autor:
Antonio de Marvao, Francesca Girolami, Antonis Pantazis, Francesco Mazzarotto, A. John Baksi, James S. Ware, Kathryn A. McGurk, Iacopo Olivotto, Megan H. Hawley, Angharad M. Roberts, Sanjay K Prasad, Roddy Walsh, Elisabetta Cerbai, Paul J.R. Barton, Beatrice Boschi, Ben Statton, Soha Romeih, Leander Beekman, Elisabeth M. Lodder, Declan P. O'Regan, Matteo Beltrami, Connie R. Bezzina, Magdi H. Yacoub, Birgit Funke, Mona Allouba, Yasmine Aguib, Stuart A. Cook
Publikováno v:
Genetics in Medicine
Genetics in medicine, 23(5), 856-864. Lippincott Williams and Wilkins
Genetics in medicine, 23(5), 856-864. Lippincott Williams and Wilkins
Purpose: To characterize the genetic architecture of left ventricular noncompaction (LVNC) and investigate the extent to which it may represent a distinct pathology or a secondary phenotype associated with other cardiac diseases. Methods: We performe
Autor:
Carolyn Y. Ho, Euan A. Ashley, James S. Ware, Sharlene M. Day, Sara Saberi, Joseph W. Rossano, Samuel G. Wittekind, Daniel Jacoby, Alexandre C. Pereira, Adam S. Helms, Iacopo Olivotto, Steven D. Colan, Michelle Michels, Jodie Ingles, Larry Han, Christopher Semsarian, Nicholas A Marston
Publikováno v:
European Heart Journal, 42(20), 1988-1996. Oxford University Press
Aims Childhood-onset hypertrophic cardiomyopathy (HCM) is far less common than adult-onset disease, thus natural history is not well characterized. We aim to describe the characteristics and outcomes of childhood-onset HCM. Methods and results We per
Autor:
Daniel J Hammersley, Rachel J Buchan, Amrit S Lota, Lukas Mach, Richard E Jones, Brian P Halliday, Upasana Tayal, Devendra Meena, Abbas Dehghan, Ioanna Tzoulaki, A John Baksi, Antonis Pantazis, Angharad M Roberts, Sanjay K Prasad, James S Ware
Publikováno v:
Open Heart, Vol 9, Iss 1 (2022)
Open Heart
Open Heart
Objectives(1) To evaluate the prevalence and hospitalisation rate of COVID-19 infections among patients with dilated cardiomyopathy (DCM) and hypertrophic cardiomyopathy (HCM) in the Royal Brompton and Harefield Hospital Cardiovascular Research Centr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b6939ced29dfe3ea05cea09119e10751
http://hdl.handle.net/10044/1/96212
http://hdl.handle.net/10044/1/96212
Autor:
Sara Saberi, Carolyn Y. Ho, Euan A. Ashley, Iacopo Olivotto, Sharlene M. Day, Steven D. Colan, Jodie Ingles, Christopher Semsarian, Alexandre C. Pereira, Neal K. Lakdawala, Larry Han, Peter Marstrand, James S. Ware, Michelle Michels, Adam S. Helms, Daniel Jacoby, Samuel G. Wittekind
Publikováno v:
Circulation, 141(17), 1371-1383. Lippincott Williams & Wilkins
Background: The term “end stage” has been used to describe hypertrophic cardiomyopathy (HCM) with left ventricular systolic dysfunction (LVSD), defined as occurring when left ventricular ejection fraction is Methods: Data from 11 high-volume HCM
Autor:
Upasana Tayal, Amrit Lota, John G.F. Cleland, Amal Muthumala, Michael P. Frenneaux, John Gregson, Sanjay K Prasad, Suzan Hatipoglu, Ramasamy Manivarmane, Ravi Assomull, Stuart A. Cook, Ricardo Wage, James S. Ware, Cemil Izgi, Andrew D Scott, Dudley J. Pennell, Jason Dungu, Brian P Halliday, Simon Newsome
Publikováno v:
European Journal of Heart Failure. 22:1160-1170
Aims:\ud There is an important need for better biomarkers to predict left ventricular (LV) remodelling in dilated cardiomyopathy (DCM). We undertook a comprehensive assessment of cardiac structure and myocardial composition to determine predictors of
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:
Jasper J. van der Smagt, Gemma Correnti, Diane Fatkin, E. Haan, Paul G.A. Volders, Jodie Ingles, Euan A. Ashley, Nicola Whiffin, Laura Yeates, Daniela Q.C.M. Barge-Schaapveld, Nicholas Pachter, Jan D. H. Jongbloed, Jaap I. van Waning, Arthur van den Wijngaard, Ahmet Adiyaman, Belinda Gray, Ben Corden, Victoria N. Parikh, Chloe M. Reuter, Amrit Lota, Maarten P. van den Berg, Johan Duflou, Luisa Marsili, Freyja H.M. van Lint, Ahmad S. Amin, Matthew T. Wheeler, Christopher Semsarian, Charlotte Burns, James S. Ware, Michael Fietz, Marianne Bootsma, Carlo Marcelis, Jitendra K. Vohra, Rogier A. Oldenburg, Dominica Zentner, Arthur A.M. Wilde, Laurens P Bosman, Arnaud D. Hauer, Gijs van Woerden, J. Peter van Tintelen, Edgar T. Hoorntje, R. Nils Planken, Richard D. Bagnall, Anneke M. van Mil, Gerard J. te Meerman, Hugh J. McCarthy, Ruben N. Eppinga, T. Thompson, Lien Lam
BackgroundTruncating variants in desmoplakin (DSPtv) are an important cause of arrhythmogenic cardiomyopathy (ACM), however the genetic architecture and genotype-specific risk factors are incompletely understood. We evaluated phenotype, risk factors
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::715b75283d10d73969cbe1a3dbca4b57
https://doi.org/10.1101/2021.10.16.21264154
https://doi.org/10.1101/2021.10.16.21264154
Autor:
Paul Elliott, Amanda Sr Ho, Paul M. Matthews, Stéphanie Debette, Stefan T. Engelter, Philippe Amouyel, James S. Ware, Wenjia Bai, Enrico Petretto, Muralidharan Sargurupremraj, Jian Huang, Catherine Francis, Abbas Dehghan, Matthias E. Futschik
Aortic dimensions and distensibility are key risk factors for aortic aneurysms and dissections, as well as for other cardiovascular and cerebrovascular diseases. We tested genome-wide associations of ascending and descending aortic distensibility and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::24dd2f86382e33b13aefe68a93f8edbb
https://doi.org/10.1101/2021.09.01.21262202
https://doi.org/10.1101/2021.09.01.21262202
Autor:
Wenjia Bai, Hannah Meyer, Kathryn A. McGurk, Daniel Rueckert, Zeng L, MacNamara A, Bender C, James S. Ware, Freitag Df, Declan P. O'Regan, Marjola Thanaj, Nicoló Savioli, Sohler F, de Marvao A, Mielke J, Martin R. Wilkins
Diastole is the sequence of physiological events that occur in the heart during ventricular filling and principally depends on myocardial relaxation and chamber stiffness. Abnormal diastolic function is related to many cardiovascular disease processe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c5741cce842b6065fef5f8a54a7b5638
https://doi.org/10.1101/2021.06.07.21257302
https://doi.org/10.1101/2021.06.07.21257302