نتایج جستجو برای: ischemic cardiomyopathy

تعداد نتایج: 120072  

Journal: :Revista espanola de cardiologia 2007
Guillermo Romero-Farina Jaume Candell-Riera Santiago Aguadé-Bruix Joan Castell-Conesa Gustavo de León Albert Igual

INTRODUCTION AND OBJECTIVES Although it is known that the presence of myocardial viability predicts an increase in ejection fraction after revascularization in patients with ischemic cardiomyopathy, little is known about other predictive factors. The aim of this study was to identify variables that can predict an increase in ejection fraction after coronary revascularization surgery in patients...

Journal: :Channels 2010
Naomi Gronich Azad Kumar Yuwei Zhang Igor R Efimov Nikolai M Soldatov

Existing molecular knowledge base of cardiovascular diseases is rudimentary because of lack of specific attribution to cell type and function. The aim of this study was to investigate cell-specific molecular remodeling in human atrial and ventricular myocytes associated with ischemic cardiomyopathy. Our strategy combines two technological innovations, laser-capture microdissection of identified...

Journal: :Clinical pharmacology and therapeutics 2013
B Vrtovec G Poglajen M Sever L Lezaic A Socan F Haddad J C Wu

Recent trends indicate that patients with nonischemic dilated cardiomyopathy represent the largest subpopulation of heart failure patients with a significant need for alternative treatment modalities. Similar to patients with ischemic cardiomyopathy, patients with nonischemic dilated cardiomyopathy have been found to have myocardial regions with flow abnormalities, which may represent targets f...

Journal: :Circulation: Heart Failure 2019

Journal: :European Journal of Cardio-Thoracic Surgery 1997

Journal: :Journal of the American College of Cardiology 2013

Journal: :Current Cardiovascular Imaging Reports 2014

Journal: :European Journal of Cardio-Thoracic Surgery 2001

Journal: :Puerto Rico health sciences journal 2008
Nelson Escobales María J Crespo

The Syrian cardiomyopathic hamster (SCH) is an established animal model for genetic cardiomyopathy. The disease in the hamster develops through similar stages to those observed in humans with this condition. The pathophysiological basis for this condition in the hamster resides in an inherited mutation in the gene encoding for delta-sarcoglycan, a component of the dystrophin complex. Two basic ...

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