Cardiovascular Outcomes in Aortopathy: GenTAC Registry of Genetically Triggered Aortic Aneurysms and Related Conditions.
暂无分享,去创建一个
Howard K. Song | K. Eagle | S. Lemaire | D. Milewicz | H. Dietz | D. Guo | J. Weinsaft | M. Roman | W. Ravekes | K. Holmes | R. Pyeritz | S. Morris | C. Maslen | R. Shohet | F. Asch | M. Silberbach | Howard K Song | S. Markwardt | Richard B. Devereux | Siddharth K. Prakash | Rita C Milewski | R. B. Devereux | D. Guo | S. Morris | Rita C. Milewski
[1] M. Roman,et al. Hereditary thoracic aortic disease: How to save lives. , 2021, The Journal of thoracic and cardiovascular surgery.
[2] M. Mack,et al. 2020 ACC/AHA Guideline for the Management of Patients With Valvular Heart Disease: Executive Summary: A Report of the American College of Cardiology/American Heart Association Joint Committee on Clinical Practice Guidelines. , 2020, Journal of the American College of Cardiology.
[3] M. Gross,et al. Pathogenic variants in THSD4, encoding the ADAMTS-like 6 protein, predispose to inherited thoracic aortic aneurysm , 2020, Genetics in medicine : official journal of the American College of Medical Genetics.
[4] S. Body,et al. Surgical repair of bicuspid aortopathy at small diameters: Clinical and institutional factors. , 2020, The Journal of thoracic and cardiovascular surgery.
[5] Howard K. Song,et al. Open Thoracoabdominal Aortic Repair in Patients with Heritable Aortic Disease in the GenTAC Registry. , 2020, The Annals of thoracic surgery.
[6] K. Eagle,et al. Type B aortic dissection in young individuals with confirmed and presumed Heritable Thoracic Aortic Disease. , 2020, The Annals of thoracic surgery.
[7] K. Eagle,et al. Circulating interleukin-6 (IL-6) levels are associated with aortic dimensions in genetic aortic conditions , 2019, PloS one.
[8] C. Maslen,et al. The genetic basis of Turner syndrome aortopathy , 2019, American journal of medical genetics. Part C, Seminars in medical genetics.
[9] R. Pyeritz. Marfan syndrome: improved clinical history results in expanded natural history , 2018, Genetics in Medicine.
[10] S. Morris,et al. TIMP3 and TIMP1 are risk genes for bicuspid aortic valve and aortopathy in Turner syndrome , 2018, PLoS genetics.
[11] A. F. Scott,et al. Clinical Validity of Genes for Heritable Thoracic Aortic Aneurysm and Dissection. , 2018, Journal of the American College of Cardiology.
[12] B. Agnarsson,et al. The incidence and mortality of acute thoracic aortic dissection: results from a whole nation study. , 2016, European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery.
[13] S. Lemaire,et al. International Registry of Patients Carrying TGFBR1 or TGFBR2 Mutations: Results of the MAC (Montalcino Aortic Consortium). , 2016, Circulation. Cardiovascular genetics.
[14] Howard K. Song,et al. Aortic Dissection in Patients With Genetically Mediated Aneurysms: Incidence and Predictors in the GenTAC Registry. , 2016, Journal of the American College of Cardiology.
[15] D. Milewicz,et al. Recurrent Rare Genomic Copy Number Variants and Bicuspid Aortic Valve Are Enriched in Early Onset Thoracic Aortic Aneurysms and Dissections , 2016, PloS one.
[16] K. Eagle,et al. The Need for Standardized Methods for Measuring the Aorta: Multimodality Core Lab Experience From the GenTAC Registry. , 2016, JACC. Cardiovascular imaging.
[17] Howard K. Song,et al. GenTAC registry report: Gender differences among individuals with genetically triggered thoracic aortic aneurysm and dissection , 2013, American journal of medical genetics. Part A.
[18] W. Roberts,et al. Natural History of Adults With Congenitally Malformed Aortic Valves (Unicuspid or Bicuspid) , 2012, Medicine.
[19] Howard K. Song,et al. The National Registry of Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions (GenTAC): results from phase I and scientific opportunities in phase II. , 2011, American heart journal.
[20] S. Lemaire,et al. Epidemiology of thoracic aortic dissection , 2011, Nature Reviews Cardiology.
[21] S. Siu,et al. Bicuspid aortic valve disease. , 2010, Journal of the American College of Cardiology.
[22] David M. Williams,et al. 2010 ACCF/AHA/AATS/ACR/ASA/SCA/SCAI/SIR/STS/SVM Guidelines for the diagnosis and management of patients with thoracic aortic disease. A Report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines, American Association for Thoracic Surgery, Ame , 2010, Journal of the American College of Cardiology.
[23] Howard K. Song,et al. Surgical treatment of patients enrolled in the national registry of genetically triggered thoracic aortic conditions. , 2009, The Annals of thoracic surgery.
[24] J. Coselli,et al. Analysis of multigenerational families with thoracic aortic aneurysms and dissections due to TGFBR1 or TGFBR2 mutations , 2009, Journal of Medical Genetics.
[25] K. Eagle. Rationale and design of the National Registry of Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions (GenTAC). , 2009, American heart journal.
[26] George H. Thomas,et al. Aneurysm Syndromes Caused by Mutations in the TGF-β Receptor , 2006 .
[27] G. Morris,et al. Dissecting aneurysms of the aorta. , 1966, The Surgical clinics of North America.