Search research articles
Contact Us
Filters
Showing results (41-50 of 83) with videos related to
Page
of 9
Sort By:
Progress in Cardiovascular Diseases
|
January 24, 2026
The new life of myectomy in the era of myosin inhibitors
Giovanni Quarta, Roberta Cattaneo, Giacomo Bonacchi, et al.
British Journal of Haematology
|
April 23, 2013
Assessment and management of iron overload in β-thalassaemia major patients during the 21st century: a real-life experience from the Italian WEBTHAL project
Antonio Piga, Filomena Longo, Khaled M Musallam, et al.
JACC. Cardiovascular Imaging
|
November 19, 2011
Evolution and clinical importance of fibrosis in HCM
Giovanni Quarta, Agata Grasso, Ferdinando Pasquale, et al.
Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance
|
February 13, 2013
Arrhythmogenic right ventricular cardiomyopathy mimics: role of cardiovascular magnetic resonance
Giovanni Quarta, Syed I Husain, Andrew S Flett, et al.
European Journal of Internal Medicine
|
January 18, 2011
Myocardial iron overload assessed by magnetic resonance imaging (MRI)T2* in multi-transfused patients with thalassemia and acquired anemias
Alberto Fragasso, Angela Ciancio, Clara Mannarella, et al.
Heart (British Cardiac Society)
|
July 16, 2011
The long-term survival and the risks and benefits of implantable cardioverter defibrillators in patients with hypertrophic cardiomyopathy
Constantinos O'Mahony, Pier D Lambiase, Giovanni Quarta, et al.
Plos One
|
August 14, 2020
Clinical academic research in the time of Corona: A simulation study in England and a call for action
Amitava Banerjee, Michail Katsoulis, Alvina G Lai, et al.
American Journal of Hypertension
|
January 31, 2009
Evaluation of systolic properties in hypertensive patients with different degrees of diastolic dysfunction and normal ejection fraction
Sebastiano Sciarretta, Francesco Paneni, Giuseppino M Ciavarella, et al.
European Heart Journal
|
November 20, 2012
Recurrent missense mutations in TMEM43 (ARVD5) due to founder effects cause arrhythmogenic cardiomyopathies in the UK and Canada
Annika F M Haywood, Nancy D Merner, Kathy A Hodgkinson, et al.
American Journal of Medical Genetics. Part A
|
June 20, 2017
Psychiatric and cognitive characteristics of individuals with Danon disease (LAMP2 gene mutation)
Maya Yardeni, Omri Weisman, Hanna Mandel, et al.
Page
of 9
Search research articles
Search
Showing results (41-50 of 83) with videos related to
Sort By:
Page
of 9
Progress in Cardiovascular Diseases
|
January 24, 2026
The new life of myectomy in the era of myosin inhibitors
Giovanni Quarta, Roberta Cattaneo, Giacomo Bonacchi, et al.
British Journal of Haematology
|
April 23, 2013
Assessment and management of iron overload in β-thalassaemia major patients during the 21st century: a real-life experience from the Italian WEBTHAL project
Antonio Piga, Filomena Longo, Khaled M Musallam, et al.
JACC. Cardiovascular Imaging
|
November 19, 2011
Evolution and clinical importance of fibrosis in HCM
Giovanni Quarta, Agata Grasso, Ferdinando Pasquale, et al.
Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance
|
February 13, 2013
Arrhythmogenic right ventricular cardiomyopathy mimics: role of cardiovascular magnetic resonance
Giovanni Quarta, Syed I Husain, Andrew S Flett, et al.
European Journal of Internal Medicine
|
January 18, 2011
Myocardial iron overload assessed by magnetic resonance imaging (MRI)T2* in multi-transfused patients with thalassemia and acquired anemias
Alberto Fragasso, Angela Ciancio, Clara Mannarella, et al.
Heart (British Cardiac Society)
|
July 16, 2011
The long-term survival and the risks and benefits of implantable cardioverter defibrillators in patients with hypertrophic cardiomyopathy
Constantinos O'Mahony, Pier D Lambiase, Giovanni Quarta, et al.
Plos One
|
August 14, 2020
Clinical academic research in the time of Corona: A simulation study in England and a call for action
Amitava Banerjee, Michail Katsoulis, Alvina G Lai, et al.
American Journal of Hypertension
|
January 31, 2009
Evaluation of systolic properties in hypertensive patients with different degrees of diastolic dysfunction and normal ejection fraction
Sebastiano Sciarretta, Francesco Paneni, Giuseppino M Ciavarella, et al.
European Heart Journal
|
November 20, 2012
Recurrent missense mutations in TMEM43 (ARVD5) due to founder effects cause arrhythmogenic cardiomyopathies in the UK and Canada
Annika F M Haywood, Nancy D Merner, Kathy A Hodgkinson, et al.
American Journal of Medical Genetics. Part A
|
June 20, 2017
Psychiatric and cognitive characteristics of individuals with Danon disease (LAMP2 gene mutation)
Maya Yardeni, Omri Weisman, Hanna Mandel, et al.
Page
of 9