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Revista española de cardiologia, ISSN 0300-8932, 03/2016, Volume 69, Issue 3, pp. 300 - 309
... ( cardiomyopathies, channelopathies, certain aortic diseases, and other syndromes) with a number of common characteristics... 
Cardiac & Cardiovascular Systems | Life Sciences & Biomedicine | Cardiovascular System & Cardiology | Science & Technology | Brugada Syndrome - genetics | Long QT Syndrome - complications | Brugada Syndrome - diagnosis | Loeys-Dietz Syndrome - complications | Cardiomyopathy, Hypertrophic, Familial - genetics | Channelopathies - complications | Humans | Cardiovascular Diseases - therapy | Death, Sudden, Cardiac - prevention & control | Brugada Syndrome - complications | Death, Sudden, Cardiac - etiology | Cardiovascular Diseases - genetics | Marfan Syndrome - therapy | Cardiomyopathy, Hypertrophic, Familial - diagnosis | Channelopathies - diagnosis | Cardiomyopathy, Hypertrophic, Familial - complications | Cardiovascular Diseases - complications | Long QT Syndrome - diagnosis | Tachycardia, Ventricular - genetics | Cardiomyopathy, Dilated - diagnosis | Marfan Syndrome - complications | Arrhythmias, Cardiac - genetics | Cardiovascular Diseases - diagnosis | Cardiomyopathy, Dilated - genetics | Tachycardia, Ventricular - therapy | Genetic Predisposition to Disease | Tachycardia, Ventricular - complications | Arrhythmias, Cardiac - therapy | Cardiomyopathy, Dilated - complications | Loeys-Dietz Syndrome - diagnosis | Long QT Syndrome - therapy | Marfan Syndrome - genetics | Channelopathies - therapy | Loeys-Dietz Syndrome - therapy | Channelopathies - genetics | Algorithms | Cardiomyopathy, Hypertrophic, Familial - therapy | Tachycardia, Ventricular - diagnosis | Marfan Syndrome - diagnosis | Long QT Syndrome - genetics | Arrhythmias, Cardiac - complications | Arrhythmias, Cardiac - diagnosis | Loeys-Dietz Syndrome - genetics | Brugada Syndrome - therapy | Cardiomyopathy, Dilated - therapy | Practice Guidelines as Topic | Heart | Genetic aspects | Cardiovascular diseases | Index Medicus
Journal Article
Cardiovascular pathology, ISSN 1054-8807, 03/2018, Volume 33, pp. 62 - 69
Patients with Marfan (MFS) syndrome and patients with a bicuspid aortic valve (BAV) are more prone to develop aortic dilation and dissection compared to persons with a tricuspid aortic valve... 
molecular biology | histopathology | aneurysm | aorta | bicuspid aortic valve | Marfan syndrome | Cardiac & Cardiovascular Systems | Pathology | Life Sciences & Biomedicine | Cardiovascular System & Cardiology | Science & Technology | Index Medicus
Journal Article
Clinics in dermatology, ISSN 0738-081X, 2015, Volume 34, Issue 2, pp. 242 - 275
Journal Article
Journal of allergy and clinical immunology, ISSN 0091-6749, 08/2013, Volume 132, Issue 2, pp. 378 - 386
Journal Article
Journal of the American College of Cardiology, ISSN 0735-1097, 02/2016, Volume 67, Issue 6, pp. 618 - 626
Journal Article