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Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
October 2, 2008
The many faces of aggressive aortic pathology: Loeys-Dietz syndrome
J J J Aalberts, M P van den Berg, J E H Bergman, et al.
Neuropediatrics
|
June 10, 2005
Neonatal lactic acidosis, complex I/IV deficiency, and fetal cerebral disruption
H L M van Straaten, J P van Tintelen, J M F Trijbels, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
December 2, 2009
Founder mutations in the Netherlands: SCN5a 1795insD, the first described arrhythmia overlap syndrome and one of the largest and best characterised families worldwide
P G Postema, M Van den Berg, J P Van Tintelen, et al.
Clinical Genetics
|
August 20, 2010
Desmin-related myopathy
K Y van Spaendonck-Zwarts, L van Hessem, J D H Jongbloed, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
March 5, 2010
Recurrent and founder mutations in the Netherlands: Extensive clinical variability in Marfan syndrome patients with a single novel recurrent fibrillin-1 missense mutation
J J J Aalberts, A G Schuurman, G Pals, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
May 29, 2019
UNRAVEL: big data analytics research data platform to improve care of patients with cardiomyopathies using routine electronic health records and standardised biobanking
A Sammani, M Jansen, M Linschoten, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
May 28, 2010
Founder mutations in hypertrophic cardiomyopathy patients in the Netherlands
I Christiaans, E A Nannenberg, D Dooijes, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
February 20, 2015
A large family characterised by nocturnal sudden death
M P van den Berg, J W Viersma, G C M Beaufort-Krol, et al.
Clinical Genetics
|
February 22, 2011
Critical appraisal of the revised Ghent criteria for diagnosis of Marfan syndrome
T Radonic, P de Witte, M Groenink, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
May 3, 2011
Recurrent and founder mutations in the Netherlands: cardiac Troponin I (TNNI3) gene mutations as a cause of severe forms of hypertrophic and restrictive cardiomyopathy
A van den Wijngaard, P Volders, J P Van Tintelen, et al.
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of 5
Search research articles
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Showing results (21-30 of 44) with videos related to
Sort By:
Page
of 5
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
October 2, 2008
The many faces of aggressive aortic pathology: Loeys-Dietz syndrome
J J J Aalberts, M P van den Berg, J E H Bergman, et al.
Neuropediatrics
|
June 10, 2005
Neonatal lactic acidosis, complex I/IV deficiency, and fetal cerebral disruption
H L M van Straaten, J P van Tintelen, J M F Trijbels, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
December 2, 2009
Founder mutations in the Netherlands: SCN5a 1795insD, the first described arrhythmia overlap syndrome and one of the largest and best characterised families worldwide
P G Postema, M Van den Berg, J P Van Tintelen, et al.
Clinical Genetics
|
August 20, 2010
Desmin-related myopathy
K Y van Spaendonck-Zwarts, L van Hessem, J D H Jongbloed, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
March 5, 2010
Recurrent and founder mutations in the Netherlands: Extensive clinical variability in Marfan syndrome patients with a single novel recurrent fibrillin-1 missense mutation
J J J Aalberts, A G Schuurman, G Pals, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
May 29, 2019
UNRAVEL: big data analytics research data platform to improve care of patients with cardiomyopathies using routine electronic health records and standardised biobanking
A Sammani, M Jansen, M Linschoten, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
May 28, 2010
Founder mutations in hypertrophic cardiomyopathy patients in the Netherlands
I Christiaans, E A Nannenberg, D Dooijes, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
February 20, 2015
A large family characterised by nocturnal sudden death
M P van den Berg, J W Viersma, G C M Beaufort-Krol, et al.
Clinical Genetics
|
February 22, 2011
Critical appraisal of the revised Ghent criteria for diagnosis of Marfan syndrome
T Radonic, P de Witte, M Groenink, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
May 3, 2011
Recurrent and founder mutations in the Netherlands: cardiac Troponin I (TNNI3) gene mutations as a cause of severe forms of hypertrophic and restrictive cardiomyopathy
A van den Wijngaard, P Volders, J P Van Tintelen, et al.
Page
of 5