[HTML][HTML] When Paying Attention Pays Back: Missense Mutation c. 1006G> A p.(Val336Ile) in PRKAG2 Gene Causing Left Ventricular Hypertrophy and Conduction …
E Micaglio, L Tondi, S Benedetti… - International …, 2024 - pmc.ncbi.nlm.nih.gov
PRKAG2 cardiomyopathy is a rare genetic disorder that manifests early in life with an
autosomal dominant inheritance pattern. It harbors left ventricular hypertrophy (LVH) …
autosomal dominant inheritance pattern. It harbors left ventricular hypertrophy (LVH) …
Cardiovascular magnetic resonance insights into anomalies of the mitral valve apparatus in Fabry cardiomyopathy and hypertrophic cardiomyopathy
Background and aims Despite different etiopathogenesis, Fabry Disease cardiomyopathy
(FDc) and sarcomeric hypertrophic cardiomyopathy (HCM) share a similar hypertrophic …
(FDc) and sarcomeric hypertrophic cardiomyopathy (HCM) share a similar hypertrophic …
[HTML][HTML] Accelerated Cartesian cardiac T2 mapping based on a calibrationless locally low-rank tensor constraint
J Gao, Y Gong, X Tang, H Chen, Z Chen… - … Imaging in Medicine …, 2024 - pmc.ncbi.nlm.nih.gov
Background Cardiac T2 mapping is a valuable tool for diagnosing myocardial edema,
inflammation, and infiltration, yet its spatial resolution is limited by the single-shot balanced …
inflammation, and infiltration, yet its spatial resolution is limited by the single-shot balanced …