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Author/Creator Elliott, Perry M

1. 126 Advanced Assessment of Cardiac Morphology and Prediction of Gene Carriage by CMR in Hypertrophic Cardiomyopathy - The HCMNET/UCL Collaboration. (31st May 2014)

Authors:
Captur, Gaby; Mohun, Timothy J; Finocchiaro, Gherardo; Wilson, Robert; Levine, Jonathan; Conner, Lauren; Lopes, Luis; Patel, Vimal; Sado, Daniel M; Li, Chunming; Bassett, Paul; Herrey, Anna; Tome Esteban, Maite; McKenna, William J; Seidman, Christine; Muthurangu, Vivek; Bluemke, David A; Ho, Caro...
Journal:
Heart
Issue:
Volume 100:(2014)Supplement 3
Page Start:
A72
Record Type:
Journal Article
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2. 2018 ESC Guidelines for the diagnosis and management of syncope. (19th March 2018)

Authors:
Brignole, Michele; Moya, Angel; de Lange, Frederik J; Deharo, Jean-Claude; Elliott, Perry M; Fanciulli, Alessandra; Fedorowski, Artur; Furlan, Raffaello; Kenny, Rose Anne; Martín, Alfonso; Probst, Vincent; Reed, Matthew J; Rice, Ciara P; Sutton, Richard; Ungar, Andrea; van Dijk, J Gert
Journal:
European heart journal
Issue:
Volume 39:Number 21(2018)
Page Start:
1883
Record Type:
Journal Article
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5. A validation study of the 2003 American College of Cardiology/European Society of Cardiology and 2011 American College of Cardiology Foundation/American Heart Association risk stratification and treatment algorithms for sudden cardiac death in patients with hypertrophic cardiomyopathy. Issue 8 (22nd January 2013)

Authors:
O'Mahony, Constantinos; Tome-Esteban, Maite; Lambiase, Pier D; Pantazis, Antonios; Dickie, Shaughan; McKenna, William J; Elliott, Perry M
Journal:
Heart
Issue:
Volume 99:Issue 8(2013)
Page Start:
534
Record Type:
Journal Article
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6. Agalsidase alfa versus agalsidase beta for the treatment of Fabry disease: an international cohort study. Issue 5 (7th February 2018)

Authors:
Arends, Maarten; Biegstraaten, Marieke; Wanner, Christoph; Sirrs, Sandra; Mehta, Atul; Elliott, Perry M; Oder, Daniel; Watkinson, Oliver T; Bichet, Daniel G; Khan, Aneal; Iwanochko, Mark; Vaz, Frédéric M; van Kuilenburg, André B P; West, Michael L; Hughes, Derralynn A; Hollak, Carla E M
Journal:
Journal of medical genetics
Issue:
Volume 55:Issue 5(2018)
Page Start:
351
Record Type:
Journal Article
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9. Alpha-protein kinase 3 (ALPK3) truncating variants are a cause of autosomal dominant hypertrophic cardiomyopathy. (15th July 2021)

Authors:
Lopes, Luis R; Garcia-Hernández, Soledad; Lorenzini, Massimiliano; Futema, Marta; Chumakova, Olga; Zateyshchikov, Dmitry; Isidoro-Garcia, Maria; Villacorta, Eduardo; Escobar-Lopez, Luis; Garcia-Pavia, Pablo; Bilbao, Raquel; Dobarro, David; Sandin-Fuentes, Maria; Catalli, Claudio; Gener Querol, Bl...
Journal:
European heart journal
Issue:
Volume 42:Number 32(2021)
Page Start:
3063
Record Type:
Journal Article
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