Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Samir Arnaout"'
Autor:
Marwan M. Refaat, Sylvana Hassanieh, Jad A. Ballout, Patrick Zakka, Mostafa Hotait, Athar Khalil, Fadi Bitar, Mariam Arabi, Samir Arnaout, Hadi Skouri, Antoine Abchee, Bernard Abi-Saleh, Maurice Khoury, Andreas Massouras, Georges Nemer
Publikováno v:
BMC Medical Genomics, Vol 12, Iss 1, Pp 1-11 (2019)
Abstract Background Cardiomyopathies affect more than 0.5% of the general population. They are associated with high risk of sudden cardiac death, which can result from either heart failure or electrical abnormalities. Although different mechanisms un
Externí odkaz:
https://doaj.org/article/714bffd2095d4d429574eb50cab5284a
Autor:
Samir Arnaout, Hanady R. Samaha, Julien Succar, Imad Bou-Akl, Khaled M. Musallam, Ali T. Taher
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 3, Iss 1, Pp e2011023-e2011023 (2011)
Several factors have been proposed to explain the persistence of a high incidence of venous thromboembolism worldwide with its associated morbidity and mortality. Underutilization of anticoagulants and failure of adherence to thromboprophylaxis guide
Externí odkaz:
https://doaj.org/article/efb3a3e7c2774589b6cc794ed30a37bc
Publikováno v:
Journal of Medical Case Reports, Vol 17, Iss 1, Pp 1-5 (2023)
Abstract Background Several factors increase the risk of right-sided endocarditis. The tricuspid valve is usually involved in right-sided endocarditis cases. Infective endocarditis of the pulmonic valve is rare, and few cases of pulmonic valve endoca
Externí odkaz:
https://doaj.org/article/7c390706ee024737a0303326d479fbec
Publikováno v:
Archives of Clinical and Medical Case Reports.
Autor:
Ali T. Taher, Mostafa Hotait, Patrick Zakka, Miran A. Jaffa, Joseph Elias, Farah Abdulhai, Rayan Bou-Fakhredin, Samir Arnaout, Marwan M. Refaat
Publikováno v:
Annals of hematology. 100(10)
Beta-thalassemia intermedia (β-TI) is associated with vascular dysfunction. We used digital thermal monitoring (DTM), a non-invasive tool that evaluates vascular function based on changes in fingertip temperature during and after cuff occlusion on
Autor:
Wael Almahmeed, Samir Arnaout, Aletta E. Schutte, Dorairaj Prabhakaran, N. E. Zvartau, Markus P. Schlaich, Julia Zhernakova
Publikováno v:
Current medical research and opinion. 36(12)
Multiple pharmacologic strategies are currently available to lower blood pressure (BP). Renin-angiotensin system (RAS)-inhibitors, calcium channel blockers and diuretics are widely recommended as first line therapies. Sympathetic activation is an imp
Autor:
Samir Arnaout, Georges Nemer, Ossama K. Abou Hassan, Steven R. DePalma, Manal Batrawi, Fadi Bitar, James S. Ware, Antoine Abchee, Mariam Arabi, Jonathan G. Seidman, Athar Khalil, Akl C. Fahed, Christine E. Seidman, Barbara McDonough
Publikováno v:
Circulation. Cardiovascular Genetics
Supplemental Digital Content is available in the text.
Background: Cardiac troponin I (TNNI3) gene mutations account for 3% of hypertrophic cardiomyopathy and carriers have a heterogeneous phenotype, with increased risk of sudden cardiac death (
Background: Cardiac troponin I (TNNI3) gene mutations account for 3% of hypertrophic cardiomyopathy and carriers have a heterogeneous phenotype, with increased risk of sudden cardiac death (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9338ff1ab859680e0a92cfd91bbe141b
http://hdl.handle.net/10044/1/82743
http://hdl.handle.net/10044/1/82743
Autor:
Rita Nemr, Samir Arnaout, Antoine Sarkis, Mounzer Saleh, Emile Andari, Elie Chammas, Sami T. Azar, Selim Jambart
Publikováno v:
Current diabetes reviews. 16(8)
Background: Cardiovascular disease (CVD), the main macro vascular complication of type 2 diabetes (T2D), increases the risk of death significantly in patients with T2D. Introduction: Most of the patients with T2D do not have obvious CVD symptoms. Due
Autor:
Samir Arnaout, Mariam Arabi, Athar Khalil, Jonathan G. Seidman, Akl C. Fahed, Steven R. DePalma, Christine E. Seidman, Manal Batrawi, James S. Ware, Fadi Bitar, Georges Nemer, Antoine Abche, Barbara McDonough
Publikováno v:
Circulation Research. 125
Hypertrophic Cardiomyopathy (HCM) occurs in 1 of every 500 people and has a wide phenotypic variability. In the majority of cases, HCM is caused by known mutations in genes that code for sarcomere proteins. Although gene testing is widely available f
Autor:
Andreas Massouras, Sylvana Hassanieh, Mostafa Hotait, Fadi Bitar, Georges Nemer, Maurice Khoury, Patrick Zakka, Bernard Abi-Saleh, Samir Arnaout, Mariam Arabi, Jad Ballout, Marwan M. Refaat, Antoine Abchee, Athar Khalil, Hadi Skouri
Publikováno v:
BMC Medical Genomics, Vol 12, Iss 1, Pp 1-11 (2019)
BMC Medical Genomics
BMC Medical Genomics
Background Cardiomyopathies affect more than 0.5% of the general population. They are associated with high risk of sudden cardiac death, which can result from either heart failure or electrical abnormalities. Although different mechanisms underlie th