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Current Opinion in Cardiology
|
April 7, 2007
Molecular genetics of arrhythmogenic right ventricular cardiomyopathy: emerging horizon?
J Peter van Tintelen, Robert Mw Hofstra, Ans Cp Wiesfeld, et al.
European Journal of Cardio-Thoracic Surgery : Official Journal of the European Association for Cardio-Thoracic Surgery
|
June 3, 2008
Prophylactic aortic root surgery in patients with Marfan syndrome: 10 years' experience with a protocol based on body surface area
Jan J J Aalberts, Tjalling W Waterbolk, J Peter van Tintelen, et al.
European Journal of Heart Failure
|
October 19, 2010
Familial dilated cardiomyopathy: another risk factor for anthracycline-induced cardiotoxicity?
Maarten P van den Berg, Karin Y van Spaendonck-Zwarts, Dirk J van Veldhuisen, et al.
European Journal of Human Genetics : EJHG
|
December 20, 2012
Clinical utility gene card for: dilated cardiomyopathy (CMD)
Anna Posafalvi, Johanna C Herkert, Richard J Sinke, et al.
Stem Cell Research
|
March 5, 2022
Generation of human induced pluripotent stem cell (iPSC) lines derived from five patients carrying the pathogenic phospholamban-R14del (PLN-R14del) variant and three non-carrier family members
Nishka Mittal, Jaydev Dave, Magdalena Harakalova, et al.
European Journal of Human Genetics : EJHG
|
June 6, 2013
Clinical utility gene card for: arrhythmogenic right ventricular cardiomyopathy (ARVC)
Wouter P Te Rijdt, Jan Dh Jongbloed, Rudolf A de Boer, et al.
Cardiovascular Research
|
September 29, 2017
Arrhythmogenic cardiomyopathy: pathology, genetics, and concepts in pathogenesis
Edgar T Hoorntje, Wouter P Te Rijdt, Cynthia A James, et al.
Molecular Genetics & Genomic Medicine
|
November 29, 2018
Autosomal dominant Marfan syndrome caused by a previously reported recessive FBN1 variant
Eline Overwater, Rifka Efrat, Daniela Q C M Barge-Schaapveld, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
February 8, 2019
[Hypertrophic cardiomyopathy]
Beau van Driel, Folkert W Asselbergs, Rudolf A de Boer, et al.
European Journal of Human Genetics : EJHG
|
November 24, 2021
A tailored approach to informing relatives at risk of inherited cardiac conditions: results of a randomised controlled trial
Lieke M van den Heuvel, Yvonne M Hoedemaekers, Annette F Baas, et al.
Page
of 24
Search research articles
Search
Showing results (31-40 of 232) with videos related to
Sort By:
Page
of 24
Current Opinion in Cardiology
|
April 7, 2007
Molecular genetics of arrhythmogenic right ventricular cardiomyopathy: emerging horizon?
J Peter van Tintelen, Robert Mw Hofstra, Ans Cp Wiesfeld, et al.
European Journal of Cardio-Thoracic Surgery : Official Journal of the European Association for Cardio-Thoracic Surgery
|
June 3, 2008
Prophylactic aortic root surgery in patients with Marfan syndrome: 10 years' experience with a protocol based on body surface area
Jan J J Aalberts, Tjalling W Waterbolk, J Peter van Tintelen, et al.
European Journal of Heart Failure
|
October 19, 2010
Familial dilated cardiomyopathy: another risk factor for anthracycline-induced cardiotoxicity?
Maarten P van den Berg, Karin Y van Spaendonck-Zwarts, Dirk J van Veldhuisen, et al.
European Journal of Human Genetics : EJHG
|
December 20, 2012
Clinical utility gene card for: dilated cardiomyopathy (CMD)
Anna Posafalvi, Johanna C Herkert, Richard J Sinke, et al.
Stem Cell Research
|
March 5, 2022
Generation of human induced pluripotent stem cell (iPSC) lines derived from five patients carrying the pathogenic phospholamban-R14del (PLN-R14del) variant and three non-carrier family members
Nishka Mittal, Jaydev Dave, Magdalena Harakalova, et al.
European Journal of Human Genetics : EJHG
|
June 6, 2013
Clinical utility gene card for: arrhythmogenic right ventricular cardiomyopathy (ARVC)
Wouter P Te Rijdt, Jan Dh Jongbloed, Rudolf A de Boer, et al.
Cardiovascular Research
|
September 29, 2017
Arrhythmogenic cardiomyopathy: pathology, genetics, and concepts in pathogenesis
Edgar T Hoorntje, Wouter P Te Rijdt, Cynthia A James, et al.
Molecular Genetics & Genomic Medicine
|
November 29, 2018
Autosomal dominant Marfan syndrome caused by a previously reported recessive FBN1 variant
Eline Overwater, Rifka Efrat, Daniela Q C M Barge-Schaapveld, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
February 8, 2019
[Hypertrophic cardiomyopathy]
Beau van Driel, Folkert W Asselbergs, Rudolf A de Boer, et al.
European Journal of Human Genetics : EJHG
|
November 24, 2021
A tailored approach to informing relatives at risk of inherited cardiac conditions: results of a randomised controlled trial
Lieke M van den Heuvel, Yvonne M Hoedemaekers, Annette F Baas, et al.
Page
of 24