Results 101 to 110 of about 2,884 (194)

Abnormal Flow Conditions Promote Endocardial Fibroelastosis Via Endothelial-to-Mesenchymal Transition, Which Is Responsive to Losartan Treatment. [PDF]

open access: yesJACC Basic Transl Sci, 2021
Oh NA   +8 more
europepmc   +1 more source

Mitral valve orifice area predicts outcome after biventricular repair in patients with hypoplastic left ventricles

open access: yesJournal of Cardiovascular Magnetic Resonance
: Background: Identification of risk factors for biventricular (BiV) repair in children with hypoplastic left ventricles (HLV) has been challenging.
David Liddle   +9 more
doaj   +1 more source

Recessive ciliopathy mutations in primary endocardial fibroelastosis: a rare neonatal cardiomyopathy in a case of Alstrom syndrome. [PDF]

open access: yesJ Mol Med (Berl), 2021
Zhao Y   +24 more
europepmc   +1 more source

Wide variation in shape of hypoplastic left ventricles undergoing recruitment and biventricular repair: A statistical shape modeling study

open access: yesJournal of Cardiovascular Magnetic Resonance
: Background: Patients with hypoplastic left ventricles (LV) who undergo volume-loading procedures (recruitment, biventricular [BIV] repair) are at risk for adverse outcomes, including heart failure and death.
Isabel R. Barnet   +8 more
doaj   +1 more source

Endocardial fibroelastosis and dilated cardiomyopathy - the past and future of the interface between histology and genetics. [PDF]

open access: yesRom J Morphol Embryol, 2020
Luca AC   +10 more
europepmc   +1 more source

Cardiac Disease of Obscure Origin in Africa [PDF]

open access: yes, 1958
A Central African Journal of Medicine (CAJM) article on heart disease in Africa.Within recent years a number of papers have emanated from East, West, Central and South Africa, all reporting a form or forms of congestive heart failure, the etiology of ...
Gelfand, Michael
core  

Cardiac pathology in a patient with a novel pathogenic variant c.703del (p.Ile235SerfsTer4) of the TAFAZZIN gene [PDF]

open access: yes
IntroductionBarth syndrome is a mitochondrial disease caused by loss-of-function mutations in the TAFAZZIN gene located on chromosome Xq28 encoding a transacylase essential for cardiolipin remodeling.
Chang, Richard   +6 more
core   +1 more source

Acute endomyocardial disease in infants and children : the relationship between acute myocarditis and endocardial fibroelastosis [PDF]

open access: yes, 1979
This prospective study of acute myocarditis (AM) and endocardial fibroelastosis (EFE) was prompted by their common occurrence in infants and children in Cape Town, and by the persisting controversy regarding the possible relationship of these two ...
Joffe, Hymie Simon
core  

Cardiac magnetic resonance imaging in congenital heart disease [PDF]

open access: yes, 2016
Deluigi, Christina   +7 more
core   +1 more source

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