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Journal of Cardiovascular Development and Disease
|
July 25, 2022
Peak Oxygen Uptake on Cardiopulmonary Exercise Test Is a Predictor for Severe Arrhythmic Events during Three-Year Follow-Up in Patients with Complex Congenital Heart Disease
Felix von Sanden, Svetlana Ptushkina, Julia Hock, et al.
Cardiology in the Young
|
August 31, 2023
Differentiating primary sarcomeric hypertrophic cardiomyopathy from Noonan syndrome: can the electrocardiogram be of use?
Robert W L Hauptmeijer, Lea Lippert, Floris E A Udink Ten Cate, et al.
European Journal of Medical Genetics
|
November 10, 2021
Management of cardiac aspects in children with Noonan syndrome - results from a European clinical practice survey among paediatric cardiologists
Cordula M Wolf, Martin Zenker, Emma Burkitt-Wright, et al.
European Journal of Cardio-Thoracic Surgery : Official Journal of the European Association for Cardio-Thoracic Surgery
|
August 25, 2022
Neointimal hyperplasia in systemic-to-pulmonary shunts of children with complex cyanotic congenital heart disease
Philip Kottmann, Julie Cleuziou, Julia Lemmer, et al.
The Journal of Clinical Investigation
|
July 4, 2007
Calsequestrin 2 (CASQ2) mutations increase expression of calreticulin and ryanodine receptors, causing catecholaminergic polymorphic ventricular tachycardia
Lei Song, Ronny Alcalai, Michael Arad, et al.
ESC Heart Failure
|
November 22, 2024
Trametinib alters contractility of paediatric Noonan syndrome-associated hypertrophic myocardial tissue slices
Jules Hamers, Payel Sen, Sarala Raj Murthi, et al.
European Journal of Medical Genetics
|
November 10, 2021
European Medical Education Initiative on Noonan syndrome: A clinical practice survey assessing the diagnosis and clinical management of individuals with Noonan syndrome across Europe
Sixto García-Miñaúr, Emma Burkitt-Wright, Alain Verloes, et al.
European Journal of Medical Genetics
|
December 13, 2021
Management of growth failure and other endocrine aspects in patients with Noonan syndrome across Europe: A sub-analysis of a European clinical practice survey
Thomas Edouard, Martin Zenker, Ingegerd Östman-Smith, et al.
Plos One
|
December 19, 2008
Cytoplasmic CUG RNA foci are insufficient to elicit key DM1 features
Warunee Dansithong, Cordula M Wolf, Partha Sarkar, et al.
Biochimica Et Biophysica Acta
|
May 6, 2010
Ablation of LKB1 in the heart leads to energy deprivation and impaired cardiac function
Niels Jessen, Ho-Jin Koh, Clifford D Folmes, et al.
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of 5
Search research articles
Search
Showing results (11-20 of 44) with videos related to
Sort By:
Page
of 5
Journal of Cardiovascular Development and Disease
|
July 25, 2022
Peak Oxygen Uptake on Cardiopulmonary Exercise Test Is a Predictor for Severe Arrhythmic Events during Three-Year Follow-Up in Patients with Complex Congenital Heart Disease
Felix von Sanden, Svetlana Ptushkina, Julia Hock, et al.
Cardiology in the Young
|
August 31, 2023
Differentiating primary sarcomeric hypertrophic cardiomyopathy from Noonan syndrome: can the electrocardiogram be of use?
Robert W L Hauptmeijer, Lea Lippert, Floris E A Udink Ten Cate, et al.
European Journal of Medical Genetics
|
November 10, 2021
Management of cardiac aspects in children with Noonan syndrome - results from a European clinical practice survey among paediatric cardiologists
Cordula M Wolf, Martin Zenker, Emma Burkitt-Wright, et al.
European Journal of Cardio-Thoracic Surgery : Official Journal of the European Association for Cardio-Thoracic Surgery
|
August 25, 2022
Neointimal hyperplasia in systemic-to-pulmonary shunts of children with complex cyanotic congenital heart disease
Philip Kottmann, Julie Cleuziou, Julia Lemmer, et al.
The Journal of Clinical Investigation
|
July 4, 2007
Calsequestrin 2 (CASQ2) mutations increase expression of calreticulin and ryanodine receptors, causing catecholaminergic polymorphic ventricular tachycardia
Lei Song, Ronny Alcalai, Michael Arad, et al.
ESC Heart Failure
|
November 22, 2024
Trametinib alters contractility of paediatric Noonan syndrome-associated hypertrophic myocardial tissue slices
Jules Hamers, Payel Sen, Sarala Raj Murthi, et al.
European Journal of Medical Genetics
|
November 10, 2021
European Medical Education Initiative on Noonan syndrome: A clinical practice survey assessing the diagnosis and clinical management of individuals with Noonan syndrome across Europe
Sixto García-Miñaúr, Emma Burkitt-Wright, Alain Verloes, et al.
European Journal of Medical Genetics
|
December 13, 2021
Management of growth failure and other endocrine aspects in patients with Noonan syndrome across Europe: A sub-analysis of a European clinical practice survey
Thomas Edouard, Martin Zenker, Ingegerd Östman-Smith, et al.
Plos One
|
December 19, 2008
Cytoplasmic CUG RNA foci are insufficient to elicit key DM1 features
Warunee Dansithong, Cordula M Wolf, Partha Sarkar, et al.
Biochimica Et Biophysica Acta
|
May 6, 2010
Ablation of LKB1 in the heart leads to energy deprivation and impaired cardiac function
Niels Jessen, Ho-Jin Koh, Clifford D Folmes, et al.
Page
of 5