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Reed E Pyeritz

Showing results (81-90 of 107) with videos related to

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Journal of the American College of Cardiology|May 13, 2022
Location of Aortic Enlargement and Risk of Type A Dissection at Smaller DiametersAsvin M Ganapathi, David N Ranney, Mark D Peterson, et al.
Chest|June 19, 2007
Is pulmonary arterial hypertension in neurofibromatosis type 1 secondary to a plexogenic arteriopathy?Douglas R Stewart, Joy D Cogan, Mordechai R Kramer, et al.
The Annals of Thoracic Surgery|July 5, 2011
Impact of image analysis methodology on diagnostic and surgical classification of patients with thoracic aortic aneurysmsDorinna D Mendoza, Minisha Kochar, Richard B Devereux, et al.
Circulation. Cardiovascular Quality and Outcomes|August 15, 2024
Acute Aortic Dissection: Observational Lessons Learned From 11 000 PatientsEduardo Bossone, Kim A Eagle, Christoph A Nienaber, et al.
The American Journal of Cardiology|September 28, 2011
Type-selective benefits of medications in treatment of acute aortic dissection (from the International Registry of Acute Aortic Dissection [IRAD])Toru Suzuki, Eric M Isselbacher, Christoph A Nienaber, et al.
Circulation. Cardiovascular Genetics|June 11, 2017
Associations of Age and Sex With Marfan Phenotype: The National Heart, Lung, and Blood Institute GenTAC (Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions) RegistryMary J Roman, Richard B Devereux, Liliana R Preiss, et al.
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation|March 18, 2025
Family functioning and health-related quality of life in children and young adults with Marfan syndromeLauren S Crafts, Lynn A Sleeper, Karen Uzark, et al.
The Journal of Thoracic and Cardiovascular Surgery|May 20, 2011
Descending aortic diameter of 5.5 cm or greater is not an accurate predictor of acute type B aortic dissectionSanti Trimarchi, Frederik H W Jonker, Stuart Hutchison, et al.
American Heart Journal|September 26, 2007
Rationale and design of a randomized clinical trial of beta-blocker therapy (atenolol) versus angiotensin II receptor blocker therapy (losartan) in individuals with Marfan syndromeRonald V Lacro, Harry C Dietz, Lisa M Wruck, et al.
American Heart Journal|October 11, 2011
The National Registry of Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions (GenTAC): results from phase I and scientific opportunities in phase IIBarbara L Kroner, H Eser Tolunay, Craig T Basson, et al.
Pageof 11

Showing results (81-90 of 107) with videos related to

Sort By:
Pageof 11
Journal of the American College of Cardiology|May 13, 2022
Location of Aortic Enlargement and Risk of Type A Dissection at Smaller DiametersAsvin M Ganapathi, David N Ranney, Mark D Peterson, et al.
Chest|June 19, 2007
Is pulmonary arterial hypertension in neurofibromatosis type 1 secondary to a plexogenic arteriopathy?Douglas R Stewart, Joy D Cogan, Mordechai R Kramer, et al.
The Annals of Thoracic Surgery|July 5, 2011
Impact of image analysis methodology on diagnostic and surgical classification of patients with thoracic aortic aneurysmsDorinna D Mendoza, Minisha Kochar, Richard B Devereux, et al.
Circulation. Cardiovascular Quality and Outcomes|August 15, 2024
Acute Aortic Dissection: Observational Lessons Learned From 11 000 PatientsEduardo Bossone, Kim A Eagle, Christoph A Nienaber, et al.
The American Journal of Cardiology|September 28, 2011
Type-selective benefits of medications in treatment of acute aortic dissection (from the International Registry of Acute Aortic Dissection [IRAD])Toru Suzuki, Eric M Isselbacher, Christoph A Nienaber, et al.
Circulation. Cardiovascular Genetics|June 11, 2017
Associations of Age and Sex With Marfan Phenotype: The National Heart, Lung, and Blood Institute GenTAC (Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions) RegistryMary J Roman, Richard B Devereux, Liliana R Preiss, et al.
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation|March 18, 2025
Family functioning and health-related quality of life in children and young adults with Marfan syndromeLauren S Crafts, Lynn A Sleeper, Karen Uzark, et al.
The Journal of Thoracic and Cardiovascular Surgery|May 20, 2011
Descending aortic diameter of 5.5 cm or greater is not an accurate predictor of acute type B aortic dissectionSanti Trimarchi, Frederik H W Jonker, Stuart Hutchison, et al.
American Heart Journal|September 26, 2007
Rationale and design of a randomized clinical trial of beta-blocker therapy (atenolol) versus angiotensin II receptor blocker therapy (losartan) in individuals with Marfan syndromeRonald V Lacro, Harry C Dietz, Lisa M Wruck, et al.
American Heart Journal|October 11, 2011
The National Registry of Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions (GenTAC): results from phase I and scientific opportunities in phase IIBarbara L Kroner, H Eser Tolunay, Craig T Basson, et al.
Pageof 11