Results 31 to 40 of about 20,708 (216)

Indirect pathological indicators for cardiac sarcoidosis on endomyocardial biopsy [PDF]

open access: yesJournal of Pathology and Translational Medicine, 2020
Background The definitive pathologic diagnosis of cardiac sarcoidosis requires observation of a granuloma in the myocardial tissue. It is common, however, to receive a “negative” report for a clinically probable case. We would like to advise pathologists
Myung-Jin Cha   +6 more
doaj   +1 more source

The XIIIth Banff Conference on Allograft Pathology: The Banff 2015 Heart Meeting Report: Improving Antibody-Mediated Rejection Diagnostics: Strengths, Unmet Needs, and Future Directions. [PDF]

open access: yes, 2017
The 13th Banff Conference on Allograft Pathology was held in Vancouver, British Columbia, Canada from October 5 to 10, 2015. The cardiac session was devoted to current diagnostic issues in heart transplantation with a focus on antibody-mediated rejection
Angelini, A   +18 more
core   +1 more source

Return to work in heart failure patients with suspected viral myocarditis

open access: yesSAGE Open Medicine, 2017
Background: Endomyocardial biopsy is considered as the gold standard in patients with suspected myocarditis. We aimed to evaluate the impact of bioptic findings on prediction of successful return to work.
Rona Reibis   +6 more
doaj   +1 more source

New perspectives to repair a broken heart [PDF]

open access: yes, 2009
The aim of cardiac cell therapy is to restore at least in part the functionality of the diseased or injured myocardium by the use of stem/ progenitor cells.
BARILE, Lucio   +9 more
core   +1 more source

CARDIAC MAGNETIC RESONANCE IMAGING IN THE DIAGNOSIS OF ACUTE MYOCARDITIS: A CLINICAL CASE AND A REVIEW OF LITERATURE

open access: yesВестник рентгенологии и радиологии, 2016
The clinical manifestations of myocarditis are extremely variable and it may commonly manifest as acute myocardial infarction. The diagnosis of acute myocarditis is frequently empiric and substantiated by the clinical picture of the disease, ECG changes,
O. M. Larina   +3 more
doaj   +1 more source

High sensitivity of late gadolinium enhancement for predicting microscopic myocardial scarring in biopsied specimens in hypertrophic cardiomyopathy. [PDF]

open access: yesPLoS ONE, 2014
BACKGROUND: Myocardial scarring can be assessed by cardiac magnetic resonance imaging with late gadolinium enhancement and by endomyocardial biopsy.
Tetsuo Konno   +9 more
doaj   +1 more source

Comparison of Ventricular Inducibility with Late Gadolinium Enhancement and Myocardial Inflammation in Endomyocardial Biopsy in Patients with Dilated Cardiomyopathy. [PDF]

open access: yesPLoS ONE, 2016
Risk stratification of patients with non-ischemic dilated cardiomyopathy remains a matter of debate in the era of device implantation.We investigated associations between histopathological findings, contrast-enhanced cardiac MRI and the inducibility of ...
Karin A L Mueller   +11 more
doaj   +1 more source

Endomyocardial biopsy using the brachial venous access route. Description of the technique and 12-year experience at 2 different centers

open access: yesREC: Interventional Cardiology (English Ed.), 2020
Introduction and objectives: Recipients of a heart transplant need to receive serial endomyocardial biopsies (EMB) to discard rejection, a procedure that is usually performed through the femoral or jugular vein. Over the last few years, we have developed
María Tamargo   +20 more
doaj   +1 more source

Targeted treatment in viral‐associated inflammatory cardiomyopathy

open access: yesClinical Case Reports, 2021
Detection of viruses like HHV‐6 in endomyocardial biopsy or serum serology of patients with myocarditis or heart failure features unresponsive to conventional heart failure therapies could be a potential targeted treatment especially in refractory cases.
Ahmad Amin   +5 more
doaj   +1 more source

Senile Systemic Amyloidosis: Clinical Features at Presentation and Outcome [PDF]

open access: yes, 2013
Background Cardiac amyloidosis is a fatal disease whose prognosis and treatment rely on identification of the amyloid type. In our aging population transthyretin amyloidosis (ATTRwt) is common and must be differentiated from other amyloid types.
Banypersad, SM   +15 more
core   +1 more source

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