Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Daniel Cheeran"'
Autor:
Zhuo Chen, Elmer Salazar, Kyle Marple, Sandeep R. Das, Alpesh Amin, Daniel Cheeran, Lakshman S. Tamil, Gopal Gupta
Publikováno v:
IEEE Journal of Translational Engineering in Health and Medicine, Vol 6, Pp 1-10 (2018)
Management of heart failure is a major health care challenge. Healthcare providers are expected to use best practices described in clinical practice guidelines, which typically consist of a long series of complex rules. For heart failure management,
Externí odkaz:
https://doaj.org/article/74a7b3454d934bcc9ef410dbb1eba741
Autor:
Daniel Cheeran, Shaida Khan, Rohan Khera, Anish Bhatt, Sonia Garg, Justin L. Grodin, Robert Morlend, Faris G. Araj, Alpesh A. Amin, Jennifer T. Thibodeau, Sandeep Das, Mark H. Drazner, Pradeep P. A. Mammen
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 6, Iss 10 (2017)
BackgroundDuchenne muscular dystrophy (DMD) is frequently complicated by development of a cardiomyopathy. Despite significant medical advances provided to DMD patients over the past 2 decades, there remains a group of DMD patients who die prematurely
Externí odkaz:
https://doaj.org/article/21f4d3e8381444da81a764e3a8805000
Autor:
Gregory Paul Milligan, Nicole Minniefield, Bharath Raju, Nishi Patel, Katherine Michelis, Johanna Van Zyl, Daniel Cheeran, Amit Alam
Publikováno v:
The American journal of cardiology. 184
Ambulatory hemodynamic monitoring has demonstrated the ability to reduce heart failure-related hospitalization, regardless of left ventricular ejection fraction; however, real-world data in a Veterans Affairs patient population are limited. The prese
Autor:
Rahul Sheth, Daniel Galvan, Hannah Lehrenbaum, Daniel Cheeran, Faris Araj, Alpesh Amin, Mark H Drazner, Vlad G Zaha, Ronald M Peshock, Pradeep P Mammen
Publikováno v:
Circulation. 144
Introduction: Cardiomyopathy is a common complication in muscular dystrophy (MD) patients, though the mechanism is not clear. Retrospective data from adults with Duchenne muscular dystrophy suggest they have reduced LV mass compared to adults with ot
Autor:
Hannah Lehrenbaum, Rahul Sheth, Daniel Cheeran, Faris Araj, Alpesh Amin, Ronald M Peshock, Mark H Drazner, Pradeep P Mammen
Publikováno v:
Circulation. 144
Introduction: Duchenne muscular dystrophy (DMD) is a rare X-linked neuromuscular disorder affecting 1:5,000 males that results in terminal injury to the skeletal muscle and the heart. Recent evidence suggests that DMD female carriers are also at incr
Publikováno v:
Resuscitation. 141:69-72
Background Cardiac troponin is routinely tested in the post-cardiac arrest setting, but its utility in identifying ischaemic aetiology and predicting left ventricular systolic dysfunction (LVSD) and survival is not known. Methods In a retrospective s
Autor:
Susan M. Joseph, Timothy Gong, Detlef Wencker, Daniel Cheeran, Shelley A. Hall, Subash Banerjee, Nicole Minniefield, Nishi Patel, Amit Alam
Publikováno v:
Circulation. 142
Background: Due to the Coronavirus Disease of 2019 pandemic many clinics began to utilize virtual visits in lieu of traditional office visits. It is unclear what effect this will have on outcomes and admission rates for heart failure (HF). We describ
Autor:
Rahul Sheth, Alpesh Amin, Faris G. Araj, Ronald M Peshock, Claudio Ramaciotti, Mark H. Drazner, Pradeep P.A. Mammen, Daniel Cheeran
Publikováno v:
Circulation. 142
Background: Duchenne muscular dystrophy (DMD) is an X-linked neuromuscular disorder characterized by progressive muscle degeneration. The leading cause of death is complications from the development of DMD-associated cardiomyopathy. The majority of D
Autor:
Mark H. Drazner, Benjamin D. Levine, Hannah Lehrenbaum, Vlad G. Zaha, Pradeep P.A. Mammen, Yunbeen Bae, Michinari Hieda, James A. de Lemos, Faris G. Araj, Daniel Cheeran, Alpesh Amin, Colby Ayers, Ronald M Peshock
Publikováno v:
Circulation. 142
Introduction: Duchenne muscular dystrophy (DMD) is an X-linked neuromuscular disorder. DMD-associated cardiomyopathy is the primary mode of premature death in the majority of male DMD patients, but the prevalence of cardiomyopathy and its clinical si
Autor:
Daniel Cheeran, James A. de Lemos, Pradeep P.A. Mammen, Faris G. Araj, Mark H. Drazner, Alpesh Amin, Xuan Jiang, Colby Ayers, Ronald M Peshock, Rahul Sheth, Anishka P Kappalayil, Vlad G. Zaha
Publikováno v:
Circulation. 142
Background: Muscular dystrophies (MD) are genetic disorders that cause progressive peripheral skeletal myopathies. The majority of MD patients will develop atrial and ventricular arrhythmias and/or an associated cardiomyopathy with a high degree of m