Results 181 to 190 of about 105,745 (208)

Arrhythmogenic cardiomyopathy mimicking cardiac amyloidosis with Waldenström macroglobulinaemia: A diagnostic challenge. [PDF]

ESC Heart Fail
Ma L, Chen L, Li J, Wang Q, Liu X, Liu X, Zhang Y, Ni M.   +7 more
europepmc   +1 more source

State-of-the-Art in Echocardiographic Strain Imaging of Arrhythmogenic Cardiomyopathy. [PDF]

J Am Soc Echocardiogr
Meredith T, Picard MH, Churchill TW, Bernard S, Bertrand PB, Sanborn DMY, Namasivayam M.   +6 more
europepmc   +1 more source

Molecular Pathogenesis of Arrhythmogenic Cardiomyopathy: Mechanisms and Therapeutic Perspectives. [PDF]

Biomolecules
Popa E, Hostiuc S.
europepmc   +1 more source

A Genome-Wide Association Study Reveals <i>Desmoglein-2</i> Predominance in Japanese Arrhythmogenic Cardiomyopathy. [PDF]

J Arrhythm
Ishikawa T, Sonehara K, Sonoda K, Hayashi K, Kato K, Nagase S, Kusano K, Aiba T, Horie M, Ohno S, Okada Y, Makita N.   +11 more
europepmc   +1 more source

Disease models and AAV therapies of <i>PKP2</i>-induced arrhythmogenic cardiomyopathy. [PDF]

Mol Ther Adv
Geerlings L, Carreras YR, Vermeer MCSC.
europepmc   +1 more source

Arrhythmogenic Cardiomyopathy [PDF]

Circulation Research, 2017
Arrhythmogenic cardiomyopathy is an inherited heart muscle disorder, predisposing to sudden cardiac death, particularly in young patients and athletes.
Cristina Basso
exaly   +3 more sources

Natural History of Arrhythmogenic Cardiomyopathy [PDF]

Journal of Clinical Medicine, 2020
Arrhythmogenic cardiomyopathy (AC) is a heart muscle disease characterized by a scarred ventricular myocardium with a distinctive propensity to ventricular arrhythmias (VAs) and sudden cardiac death, especially in young athletes.
Alberto Cipriani
exaly   +2 more sources