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American Journal of Medical Genetics. Part A
|
November 19, 2013
Screening of TGFBR1, TGFBR2, and FLNA in familial mitral valve prolapse
Jan J J Aalberts, J Peter van Tintelen, Toon Oomen, et al.
Heart Rhythm O2
|
November 11, 2024
Healthcare professionals' perspective on the acceptance of gene therapy
Lian Y Rekker, Erik Renkema, Femke Hilverda, et al.
Iscience
|
August 18, 2025
Deep representation learning of electrocardiogram reveals biological insights in cardiac phenotypes and cardiovascular diseases
Ming Wai Yeung, Rutger R van de Leur, Jan Walter Benjamins, et al.
Heart Rhythm
|
November 1, 2006
A family with Andersen-Tawil syndrome and dilated cardiomyopathy
Bas A Schoonderwoerd, Ans C P Wiesfeld, Arthur A M Wilde, et al.
Science Translational Medicine
|
September 22, 2021
Epicardial differentiation drives fibro-fatty remodeling in arrhythmogenic cardiomyopathy
Arwa Kohela, Sebastiaan J van Kampen, Tara Moens, et al.
American Journal of Medical Genetics. Part A
|
July 13, 2021
Terminal osseous dysplasia with pigmentary defects and cardiomyopathy caused by a novel FLNA variant
Lynne Rumping, Marja W Wessels, Alex V Postma, et al.
Current Heart Failure Reports
|
December 11, 2024
Artificial Intelligence Advancements in Cardiomyopathies: Implications for Diagnosis and Management of Arrhythmogenic Cardiomyopathy
Arman Salavati, C Nina van der Wilt, Martina Calore, et al.
Journal of Genetic Counseling
|
April 29, 2026
Digital genetic counseling services for cascade cardiogenetic testing
Marlies N van Lingen, Sietske A L van Till, Noor A A Giesbertz, et al.
Journal of Clinical Medicine
|
February 22, 2020
Quantitative Approach to Fragmented QRS in Arrhythmogenic Cardiomyopathy: From Disease towards Asymptomatic Carriers of Pathogenic Variants
Rob W Roudijk, Laurens P Bosman, Jeroen F van der Heijden, et al.
Plos One
|
December 19, 2017
High proportion of genetic cases in patients with advanced cardiomyopathy including a novel homozygous Plakophilin 2-gene mutation
Baerbel Klauke, Anna Gaertner-Rommel, Uwe Schulz, et al.
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of 24
Search research articles
Search
Showing results (71-80 of 232) with videos related to
Sort By:
Page
of 24
American Journal of Medical Genetics. Part A
|
November 19, 2013
Screening of TGFBR1, TGFBR2, and FLNA in familial mitral valve prolapse
Jan J J Aalberts, J Peter van Tintelen, Toon Oomen, et al.
Heart Rhythm O2
|
November 11, 2024
Healthcare professionals' perspective on the acceptance of gene therapy
Lian Y Rekker, Erik Renkema, Femke Hilverda, et al.
Iscience
|
August 18, 2025
Deep representation learning of electrocardiogram reveals biological insights in cardiac phenotypes and cardiovascular diseases
Ming Wai Yeung, Rutger R van de Leur, Jan Walter Benjamins, et al.
Heart Rhythm
|
November 1, 2006
A family with Andersen-Tawil syndrome and dilated cardiomyopathy
Bas A Schoonderwoerd, Ans C P Wiesfeld, Arthur A M Wilde, et al.
Science Translational Medicine
|
September 22, 2021
Epicardial differentiation drives fibro-fatty remodeling in arrhythmogenic cardiomyopathy
Arwa Kohela, Sebastiaan J van Kampen, Tara Moens, et al.
American Journal of Medical Genetics. Part A
|
July 13, 2021
Terminal osseous dysplasia with pigmentary defects and cardiomyopathy caused by a novel FLNA variant
Lynne Rumping, Marja W Wessels, Alex V Postma, et al.
Current Heart Failure Reports
|
December 11, 2024
Artificial Intelligence Advancements in Cardiomyopathies: Implications for Diagnosis and Management of Arrhythmogenic Cardiomyopathy
Arman Salavati, C Nina van der Wilt, Martina Calore, et al.
Journal of Genetic Counseling
|
April 29, 2026
Digital genetic counseling services for cascade cardiogenetic testing
Marlies N van Lingen, Sietske A L van Till, Noor A A Giesbertz, et al.
Journal of Clinical Medicine
|
February 22, 2020
Quantitative Approach to Fragmented QRS in Arrhythmogenic Cardiomyopathy: From Disease towards Asymptomatic Carriers of Pathogenic Variants
Rob W Roudijk, Laurens P Bosman, Jeroen F van der Heijden, et al.
Plos One
|
December 19, 2017
High proportion of genetic cases in patients with advanced cardiomyopathy including a novel homozygous Plakophilin 2-gene mutation
Baerbel Klauke, Anna Gaertner-Rommel, Uwe Schulz, et al.
Page
of 24