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The European Respiratory Journal
|
March 21, 2024
Pulmonary vascular phenotype identified in patients with <i>GDF2</i> (<i>BMP9</i>) or <i>BMP10</i> variants: an international multicentre study
Julien Grynblat, Harm Jan Bogaard, Mélanie Eyries, et al.
Journal of the American College of Cardiology
|
April 1, 2017
Autosomal Recessive Cardiomyopathy Presenting as Acute Myocarditis
Serkan Belkaya, Amy R Kontorovich, Minji Byun, et al.
The Journal of Pediatrics
|
September 18, 2010
Isolated congenital asplenia: a French nationwide retrospective survey of 20 cases
Nizar Mahlaoui, Veronique Minard-Colin, Capucine Picard, et al.
Archives of Cardiovascular Diseases
|
April 13, 2021
Catheter ablation in adults with congenital heart disease: A 15-year perspective from a tertiary centre
Victor Waldmann, Denis Amet, Alexandre Zhao, et al.
Orphanet Journal of Rare Diseases
|
May 10, 2013
Natural history of Barth syndrome: a national cohort study of 22 patients
Charlotte Rigaud, Anne-Sophie Lebre, Renaud Touraine, et al.
Journal of the American Heart Association
|
July 9, 2024
Pulmonary Hypertension Induced by Right Pulmonary Artery Occlusion: Hemodynamic Consequences of <i>Bmpr2</i> Mutation
Alban Todesco, Julien Grynblat, Kouamé Kan Firmin Akoumia, et al.
The European Respiratory Journal
|
May 26, 2022
An emerging phenotype of pulmonary arterial hypertension patients carrying <i>SOX17</i> variants
David Montani, Benoit Lechartier, Barbara Girerd, et al.
The Journal of Rheumatology
|
May 2, 2022
Health Outcomes of 215 Mothers of Children With Autoimmune Congenital Heart Block: Analysis of the French Neonatal Lupus Syndrome Registry
Imene Miniaoui, Nathalie Morel, Kateri Lévesque, et al.
The European Respiratory Journal
|
February 22, 2020
Phenotype and outcome of pulmonary arterial hypertension patients carrying a <i>TBX4</i> mutation
Pierre Thoré, Barbara Girerd, Xavier Jaïs, et al.
Respiratory Medicine and Research
|
May 11, 2026
The preponderance of genetic variations in paediatric pulmonary hypertension
Julien Grynblat, Mélanie Eyries, Marine Ambar-Akkaoui, et al.
Page
of 47
Search research articles
Search
Showing results (401-410 of 461) with videos related to
Sort By:
Page
of 47
The European Respiratory Journal
|
March 21, 2024
Pulmonary vascular phenotype identified in patients with <i>GDF2</i> (<i>BMP9</i>) or <i>BMP10</i> variants: an international multicentre study
Julien Grynblat, Harm Jan Bogaard, Mélanie Eyries, et al.
Journal of the American College of Cardiology
|
April 1, 2017
Autosomal Recessive Cardiomyopathy Presenting as Acute Myocarditis
Serkan Belkaya, Amy R Kontorovich, Minji Byun, et al.
The Journal of Pediatrics
|
September 18, 2010
Isolated congenital asplenia: a French nationwide retrospective survey of 20 cases
Nizar Mahlaoui, Veronique Minard-Colin, Capucine Picard, et al.
Archives of Cardiovascular Diseases
|
April 13, 2021
Catheter ablation in adults with congenital heart disease: A 15-year perspective from a tertiary centre
Victor Waldmann, Denis Amet, Alexandre Zhao, et al.
Orphanet Journal of Rare Diseases
|
May 10, 2013
Natural history of Barth syndrome: a national cohort study of 22 patients
Charlotte Rigaud, Anne-Sophie Lebre, Renaud Touraine, et al.
Journal of the American Heart Association
|
July 9, 2024
Pulmonary Hypertension Induced by Right Pulmonary Artery Occlusion: Hemodynamic Consequences of <i>Bmpr2</i> Mutation
Alban Todesco, Julien Grynblat, Kouamé Kan Firmin Akoumia, et al.
The European Respiratory Journal
|
May 26, 2022
An emerging phenotype of pulmonary arterial hypertension patients carrying <i>SOX17</i> variants
David Montani, Benoit Lechartier, Barbara Girerd, et al.
The Journal of Rheumatology
|
May 2, 2022
Health Outcomes of 215 Mothers of Children With Autoimmune Congenital Heart Block: Analysis of the French Neonatal Lupus Syndrome Registry
Imene Miniaoui, Nathalie Morel, Kateri Lévesque, et al.
The European Respiratory Journal
|
February 22, 2020
Phenotype and outcome of pulmonary arterial hypertension patients carrying a <i>TBX4</i> mutation
Pierre Thoré, Barbara Girerd, Xavier Jaïs, et al.
Respiratory Medicine and Research
|
May 11, 2026
The preponderance of genetic variations in paediatric pulmonary hypertension
Julien Grynblat, Mélanie Eyries, Marine Ambar-Akkaoui, et al.
Page
of 47