Natural history of cardiovascular manifestations in Marfan syndrome. - Wikidata - wikimedia - TriplyDB

Natural history of cardiovascular manifestations in Marfan syndrome.

Natural history of cardiovascular manifestations in Marfan syndrome.

http://www.wikidata.org/entity/Q33931523

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Educational paper. Connective tissue disorders with vascular involvement: from gene to therapy Adolescent BMI at Northern Israel: From Trends, to Associated Variables and Comorbidities, and to Medical Signatures.Antibiotic resistance and antibiotic sensitivity based treatment in Helicobacter pylori infection: advantages and outcome Pre- and Postoperative Imaging of the Aortic Root Altered aortic 3D hemodynamics and geometry in pediatric Marfan syndrome patients.Prevalence data on all Ghent features in a cross-sectional study of 87 adults with proven Marfan syndrome The economic impact of Marfan syndrome: a non-experimental, retrospective, population-based matched cohort study.The prevalence and clinical impact of obesity in adults with Marfan syndrome.[Modern aortic surgery in Marfan syndrome--2011].Causes and histopathology of ascending aortic disease in children and young adults.Cardiovascular Manifestation of a Family with Marfan's Syndrome.Current insights in diagnosis and management of the cardiovascular complications of Marfan's syndrome.Parenteral nutrition solution retrieved by lumbar puncture following left saphenous vein catheterization.Chest pain in adult congenital heart disease: where does it come from?Marfan syndrome: what internists and pediatric or adult cardiologists need to know.Genetic testing in aortic aneurysm disease: PRO.Current role of endovascular therapy in Marfan patients with previous aortic surgery Project report: adult congenital heart disease.The distal aorta in the Marfan syndrome.Transforming growth factor-beta signaling in thoracic aortic aneurysm development: a paradox in pathogenesis Pathophysiology of thoracic aortic aneurysm (TAA): is it not one uniform aorta? Role of embryologic origin The pathogenesis of aortopathy in Marfan syndrome and related diseases.Current and future pharmacological treatment strategies with regard to aortic disease in Marfan syndrome.A systematic review of the pharmacological management of aortic root dilation in Marfan syndrome.A patient with Marfan's syndrome presented with severe rheumatic mitral stenosis and successfully treated with percutaneous transmitral balloon commissurotomy - Report of first case.Aortic Involvement in Pediatric Marfan syndrome: A Review.Overview of current surgical strategies for aortic disease in patients with Marfan syndrome.Genetic basis of thoracic aortic aneurysms and dissections: potential relevance to abdominal aortic aneurysms.Mortality in adult congenital heart disease.Informative STR Markers for Marfan Syndrome in Birjand, Iran.Study of phenotype evolution during childhood in Marfan syndrome to improve clinical recognition.The Kid-Short Marfan Score (Kid-SMS) - an easy executable risk score for suspected paediatric patients with Marfan syndrome.Impact of aortic aneurysm on hospitalizations in patients with marfan syndrome: a multi-institutional study.Natural history of aortic root aneurysms in Marfan syndrome.Variation in identifying neonatal percutaneous central venous line position.Critical appraisal of the revised Ghent criteria for diagnosis of Marfan syndrome.A critical analysis of minor cardiovascular criteria in the diagnostic evaluation of patients with Marfan syndrome.Effect of the Antioxidant Lipoic Acid in Aortic Phenotype in a Marfan Syndrome Mouse Model.Aortic flow patterns in patients with Marfan syndrome assessed by flow-sensitive four-dimensional MRI

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Natural history of cardiovascular manifestations in Marfan syndrome.

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2001 թուականի Փետրուարին հրատարակուած գիտական յօդուած

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Natural history of cardiovascular manifestations in Marfan syndrome.

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Natural history of cardiovascular manifestations in Marfan syndrome.

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Natural history of cardiovascular manifestations in Marfan syndrome.

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Archives of Disease in Childhood

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Natural history of cardiovascular manifestations in Marfan syndrome.

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Hennekam RC

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Mulder BJ

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Naeff MS

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Offringa M

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van Karnebeek CD

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P2860

Revised diagnostic criteria for the Marfan syndrome.

Geometric method for measuring body surface area: a height-weight formula validated in infants, children, and adults.

Evolving phenotype of Marfan's syndrome.

Aortic root complications in Marfan's syndrome: identification of a lower risk group.

Congenital cardiovascular abnormalities usually "silent" until adulthood: morphologic features of the floppy mitral valve, valvular aortic stenosis, discrete subvalvular aortic stenosis, hypertrophic cardiomyopathy, sinus of Valsalva aneurysm, and t

Progression of aortic dilatation and the benefit of long-term beta-adrenergic blockade in Marfan's syndrome.

Mitral valve dimensions and motion in Marfan patients with and without mitral valve prolapse. Comparison to primary mitral valve prolapse and normal subjects.

Reassessment of echocardiographic criteria for diagnosis of mitral valve prolapse.

Aortic root dilatation and mitral valve prolapse in Marfan's syndrome: an ECHOCARDIOgraphic study.

Two-dimensional echocardiographic aortic root dimensions in normal children and adults.

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11159287

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Aparato circulatorio

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1718664

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