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The Lancet, ISSN 0140-6736, 12/2005, Volume 366, Issue 9501, pp. 1965 - 1976
Journal Article
Journal of Clinical Gastroenterology, ISSN 0192-0790, 10/2019, Volume 53, Issue 9, pp. 653 - 659
BACKGROUND AND AIMS:Prior studies have shown a high prevalence of gastrointestinal (GI) symptoms, diagnoses of functional GI diseases (FGIDs), and pelvic floor... 
UNITED-STATES | FECAL INCONTINENCE | functional GI disorders | joint hypermobility syndrome | ehlers-danlos syndrome | irritable bowel syndrome | ADULTS | functional dyspepsia | GASTROENTEROLOGY & HEPATOLOGY | Marfan syndrome | URINARY-INCONTINENCE
Journal Article
Thrombosis and Haemostasis, ISSN 0340-6245, 10/2015, Volume 114, Issue 4, pp. 748 - 756
Folic acid metabolism enzyme polymorphism are believed to be responsible for the elevation of homocysteine (HCY) concentration in the blood plasma, correlating... 
Vascular remodelling | Single nucleotide polymorphism | Cardiology | Matrix-metalloproteinases | HCY | HOMOCYSTEINE | HYPERHOMOCYSTEINEMIA | single nucleotide polymorphism | matrix-metalloproteinases | DISORDERS | AORTIC DISSECTION | DILATION | MTHFR GENE | METHYLENETETRAHYDROFOLATE REDUCTASE | METHIONINE SYNTHASE REDUCTASE | ANEURYSMS | DISEASE | vascular remodelling | PERIPHERAL VASCULAR DISEASE | HEMATOLOGY | Aneurysm, Dissecting - diagnosis | Ferredoxin-NADP Reductase - metabolism | Multivariate Analysis | Predictive Value of Tests | Up-Regulation | Aneurysm, Dissecting - genetics | Aortic Aneurysm - diagnosis | Humans | Middle Aged | Aortic Aneurysm - therapy | Male | Methylenetetrahydrofolate Reductase (NADPH2) - metabolism | Case-Control Studies | Young Adult | Aneurysm, Dissecting - enzymology | Aortic Aneurysm - blood | Methylenetetrahydrofolate Reductase (NADPH2) - genetics | Aortic Aneurysm - enzymology | Ferredoxin-NADP Reductase - genetics | Adult | Female | Marfan Syndrome - complications | Marfan Syndrome - blood | Odds Ratio | Marfan Syndrome - enzymology | Severity of Illness Index | Genetic Predisposition to Disease | Genetic Association Studies | Gene Frequency | Risk Factors | Homocysteine - blood | Logistic Models | Biomarkers - blood | Vitamin B 12 - blood | Aneurysm, Dissecting - therapy | Chi-Square Distribution | Marfan Syndrome - genetics | Homozygote | Phenotype | 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase - metabolism | Adolescent | Folic Acid - blood | Marfan Syndrome - diagnosis | 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase - genetics | Heterozygote | Polymorphism, Single Nucleotide | Aortic Aneurysm - genetics
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 11/2010, Volume 152A, Issue 11, pp. 2749 - 2755
Journal Article
BMC Medical Genetics, ISSN 1471-2350, 08/2018, Volume 19, Issue 1, pp. 155 - 7
Journal Article
JACC (Journal of the American College of Cardiology), ISSN 0735-1097, 2014, Volume 64, Issue 16, pp. 1725 - 1739
Journal Article
Canadian Journal of Cardiology, ISSN 0828-282X, 2014, Volume 30, Issue 6, pp. 577 - 589
Abstract This Canadian Cardiovascular Society position statement aims to provide succinct perspectives on key issues in the management of thoracic aortic... 
Cardiovascular | INTERNATIONAL-REGISTRY | ENDOVASCULAR REPAIR | CARDIAC & CARDIOVASCULAR SYSTEMS | PRESSURE-LOWERING DRUGS | VALVE-REPLACEMENT | ASYMPTOMATIC PATIENTS | NATURAL-HISTORY | COMPUTED-TOMOGRAPHY | AMERICAN-SOCIETY | EHLERS-DANLOS-SYNDROME | ANEURYSM REPAIR | Genetic Testing | Loeys-Dietz Syndrome - complications | Humans | Patient Care Team | Hypertension - drug therapy | Aortic Valve - surgery | Cardiac Catheterization | Ehlers-Danlos Syndrome - genetics | Exercise | Aortic Aneurysm, Thoracic - pathology | Aneurysm, Dissecting - surgery | Turner Syndrome - complications | Aneurysm, Dissecting - prevention & control | Decision Making | Risk Assessment | Coronary Artery Disease - prevention & control | Endovascular Procedures | Antihypertensive Agents - therapeutic use | Preoperative Care | Aneurysm, Ruptured - complications | Diagnostic Imaging | Ehlers-Danlos Syndrome - complications | Diet | Hydroxymethylglutaryl-CoA Reductase Inhibitors - therapeutic use | Turner Syndrome - genetics | Ehlers-Danlos Syndrome - diagnosis | Angiotensin Receptor Antagonists - therapeutic use | Smoking Cessation | Aortic Aneurysm, Thoracic - genetics | Life Style | Marfan Syndrome - surgery | Turner Syndrome - diagnosis | Patient Selection | Marfan Syndrome - drug therapy | Hypertension - prevention & control | Adult | Female | Stents | Aorta, Thoracic - pathology | Adrenergic beta-Antagonists - therapeutic use | Aneurysm, False - surgery | Aorta, Thoracic - abnormalities | Loeys-Dietz Syndrome - diagnosis | Marfan Syndrome - genetics | Quality Assurance, Health Care | Pregnancy | Aorta, Thoracic - surgery | Marfan Syndrome - diagnosis | Aortic Aneurysm, Thoracic - surgery | Loeys-Dietz Syndrome - genetics | Automobile Driving
Journal Article
ISSN 2041-1723, 2018
Journal Article
Revista Española de Cardiología (English Edition), ISSN 1885-5857, 03/2016, Volume 69, Issue 3, pp. 300 - 309
The term inherited cardiovascular disease encompasses a group of cardiovascular diseases (cardiomyopathies, channelopathies, certain aortic diseases, and other... 
Channelopathies | Muerte súbita | Canalopatías | Síndrome de Marfan | Miocardiopatías | Cardiomyopathies | Sudden cardiac death | Marfan syndrome | DIAGNOSIS | CARDIAC & CARDIOVASCULAR SYSTEMS | MANAGEMENT | POSITION STATEMENT | GUIDELINES | EUROPEAN-SOCIETY | HYPERTROPHIC CARDIOMYOPATHY | EXPERT CONSENSUS STATEMENT | ESC | CARDIOLOGY WORKING GROUP | 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
Journal Article
Circulation. Cardiovascular Genetics, ISSN 1942-325X, 06/2017, Volume 10, Issue 3, pp. e001785 - e001785
Journal Article