Cardiac and neuronal HCN channelopathies
I Rivolta, A Binda, A Masi, JC DiFrancesco - Pflügers Archiv-European …, 2020 - Springer
Hyperpolarization-activated cyclic nucleotide–gated (HCN) channels are expressed as four
different isoforms (HCN1-4) in the heart and in the central and peripheral nervous systems …
different isoforms (HCN1-4) in the heart and in the central and peripheral nervous systems …
RBM20-related cardiomyopathy: current understanding and future options
J Koelemen, M Gotthardt, LM Steinmetz… - Journal of Clinical …, 2021 - mdpi.com
Splice regulators play an essential role in the transcriptomic diversity of all eukaryotic cell
types and organ systems. Recent evidence suggests a contribution of splice-regulatory …
types and organ systems. Recent evidence suggests a contribution of splice-regulatory …
Cardiac hypertrophy at autopsy
Since cardiac hypertrophy may be considered a cause of death at autopsy, its assessment
requires a uniform approach. Common terminology and methodology to measure the heart …
requires a uniform approach. Common terminology and methodology to measure the heart …
Accurate classification of non-ischemic cardiomyopathy
Y Wang, H Jia, J Song - Current Cardiology Reports, 2023 - Springer
Abstractt Purpose of Review This article aims to review the accurate classification of non-
ischemic cardiomyopathy, including the methods, basis, subtype characteristics, and …
ischemic cardiomyopathy, including the methods, basis, subtype characteristics, and …
[PDF][PDF] Left ventricular trabeculation and noncompaction cardiomyopathy: a review
SI McFarlane - EC clinical and experimental anatomy, 2019 - researchgate.net
Hypertrabeculation and noncompaction are congenital or acquired abnormalities of
myocardial anatomy characterized by prominent trabeculations, intertrabecular recesses …
myocardial anatomy characterized by prominent trabeculations, intertrabecular recesses …
MYH7 in cardiomyopathy and skeletal muscle myopathy
Y Gao, L Peng, C Zhao - Molecular and Cellular Biochemistry, 2024 - Springer
Myosin heavy chain gene 7 (MYH7), a sarcomeric gene encoding the myosin heavy chain
(myosin-7), has attracted considerable interest as a result of its fundamental functions in …
(myosin-7), has attracted considerable interest as a result of its fundamental functions in …
Correlation between left ventricular fractal dimension and impaired strain assessed by cardiac MRI feature tracking in patients with left ventricular noncompaction and …
S Yu, X Chen, K Yang, J Wang, K Zhao, W Dong… - European …, 2022 - Springer
Objectives To investigate the correlation between the extent of excessive trabeculation
assessed by fractal dimension (FD) and myocardial contractility assessed by cardiac MRI …
assessed by fractal dimension (FD) and myocardial contractility assessed by cardiac MRI …
Dilatative Kardiomyopathien und Non-compaction-Kardiomyopathie
A Hänselmann, C Veltmann, J Bauersachs, D Berliner - Herz, 2020 - Springer
Dilated cardiomyopathy (DCM) is the most common form of cardiomyopathy and one of the
most common causes of heart failure. It is characterized by left or biventricular dilation and a …
most common causes of heart failure. It is characterized by left or biventricular dilation and a …
Genetics and clinical features of noncompaction cardiomyopathy in the fetal population
H Sun, X Hao, X Wang, X Zhou, Y Zhang… - Frontiers in …, 2021 - frontiersin.org
Objectives: Noncompaction Cardiomyopathy (NCCM) has been classified as primary
genetic cardiomyopathy and has gained increasing clinical awareness; however, little is …
genetic cardiomyopathy and has gained increasing clinical awareness; however, little is …
A systematic review of Ebstein's anomaly with left ventricular noncompaction
Traditional definitions of Ebstein's anomaly (EA) and left ventricular noncompaction (LVNC),
two rare congenital heart defects (CHDs), confine disease to either the right or left heart …
two rare congenital heart defects (CHDs), confine disease to either the right or left heart …