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Perry Elliott

Showing results (51-60 of 156) with videos related to

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JACC. Clinical Electrophysiology|December 24, 2021
Reply: Myotonic Dystrophy and Conduction DiseaseAntonio Creta, Rui Providência, Thomas Gossios, et al.
Heart (British Cardiac Society)|September 6, 2011
Prevalence of Anderson-Fabry disease in patients with hypertrophic cardiomyopathy: the European Anderson-Fabry Disease surveyPerry Elliott, Robert Baker, Ferdinando Pasquale, et al.
Bioinformatics (Oxford, England)|June 19, 2016
The structural effects of mutations can aid in differential phenotype prediction of beta-myosin heavy chain (Myosin-7) missense variantsNouf S Al-Numair, Luis Lopes, Petros Syrris, et al.
BMJ (Clinical Research Ed.)|August 13, 2015
How to develop a more accurate risk prediction model when there are few eventsMenelaos Pavlou, Gareth Ambler, Shaun R Seaman, et al.
BMJ Open|October 29, 2023
Detecting transthyretin amyloid cardiomyopathy (ATTR-CM) using machine learning: an evaluation of the performance of an algorithm in a UK settingCarmen Tsang, Ahsan Huda, Max Norman, et al.
Metabolomics : Official Journal of the Metabolomic Society|April 13, 2016
A targeted metabolomics assay for cardiac metabolism and demonstration using a mouse model of dilated cardiomyopathyJames A West, Abdelaziz Beqqali, Zsuzsanna Ament, et al.
Plos One|January 12, 2018
Identifying unmet clinical need in hypertrophic cardiomyopathy using national electronic health recordsMar Pujades-Rodriguez, Oliver P Guttmann, Arturo Gonzalez-Izquierdo, et al.
Cardiovascular Pathology : the Official Journal of the Society for Cardiovascular Pathology|July 28, 2009
A detailed pathologic examination of heart tissue from three older patients with Anderson-Fabry disease on enzyme replacement therapyMary N Sheppard, Paul Cane, Richard Florio, et al.
Journal of Translational Medicine|May 13, 2022
Recommendations for addressing the translational gap between experimental and clinical research on amyloid diseasesMiriam Solomon, Vito Foderà, Annette Eva Langkilde, et al.
Journal of Inherited Metabolic Disease|September 28, 2011
Pregnancy and its management in women with GSD type III - a single centre experienceRadha Ramachandran, Yehani Wedatilake, Caroline Coats, et al.
Pageof 16

Showing results (51-60 of 156) with videos related to

Sort By:
Pageof 16
JACC. Clinical Electrophysiology|December 24, 2021
Reply: Myotonic Dystrophy and Conduction DiseaseAntonio Creta, Rui Providência, Thomas Gossios, et al.
Heart (British Cardiac Society)|September 6, 2011
Prevalence of Anderson-Fabry disease in patients with hypertrophic cardiomyopathy: the European Anderson-Fabry Disease surveyPerry Elliott, Robert Baker, Ferdinando Pasquale, et al.
Bioinformatics (Oxford, England)|June 19, 2016
The structural effects of mutations can aid in differential phenotype prediction of beta-myosin heavy chain (Myosin-7) missense variantsNouf S Al-Numair, Luis Lopes, Petros Syrris, et al.
BMJ (Clinical Research Ed.)|August 13, 2015
How to develop a more accurate risk prediction model when there are few eventsMenelaos Pavlou, Gareth Ambler, Shaun R Seaman, et al.
BMJ Open|October 29, 2023
Detecting transthyretin amyloid cardiomyopathy (ATTR-CM) using machine learning: an evaluation of the performance of an algorithm in a UK settingCarmen Tsang, Ahsan Huda, Max Norman, et al.
Metabolomics : Official Journal of the Metabolomic Society|April 13, 2016
A targeted metabolomics assay for cardiac metabolism and demonstration using a mouse model of dilated cardiomyopathyJames A West, Abdelaziz Beqqali, Zsuzsanna Ament, et al.
Plos One|January 12, 2018
Identifying unmet clinical need in hypertrophic cardiomyopathy using national electronic health recordsMar Pujades-Rodriguez, Oliver P Guttmann, Arturo Gonzalez-Izquierdo, et al.
Cardiovascular Pathology : the Official Journal of the Society for Cardiovascular Pathology|July 28, 2009
A detailed pathologic examination of heart tissue from three older patients with Anderson-Fabry disease on enzyme replacement therapyMary N Sheppard, Paul Cane, Richard Florio, et al.
Journal of Translational Medicine|May 13, 2022
Recommendations for addressing the translational gap between experimental and clinical research on amyloid diseasesMiriam Solomon, Vito Foderà, Annette Eva Langkilde, et al.
Journal of Inherited Metabolic Disease|September 28, 2011
Pregnancy and its management in women with GSD type III - a single centre experienceRadha Ramachandran, Yehani Wedatilake, Caroline Coats, et al.
Pageof 16