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Characterization and Clinical Management of Dilated Cardiomyopathy

Dilated cardiomyopathy (DCM) is a particular phenotype of non-ischemic systolic heart failure, frequently recognizing a genetic background and affecting relatively young patients with few comorbidities. Nowadays, long-term survival of DCM patients has been markedly improved due to an early diagnosis...

Szczegółowa specyfikacja

Zapisane w:
Format: Online
Język:angielski
Wydane: MDPI - Multidisciplinary Digital Publishing Institute 2021
Hasła przedmiotowe:
SCN5A
cardiac sodium channel
cardiac channelopathy
dilated cardiomyopathy
precision medicine
arrhythmias
atrial fibrillation
cardiomyopathy
heart failure
supraventricular arrhythmia
systolic dysfunction
tachycardiomyopathy
ventricular arrhythmia
left atrial strain
cardiac resynchronization therapy
muscular dystrophy
calcium
heart
gene therapy
phospholamban
Serca2a
mdx
oxidative stress
membrane stabilization
left ventricular noncompaction
congenital heart disease
congestive heart failure
non-ischemic cardiomyopathy
genetics
desmin
mitochondrial dysfunction
myopathy
whole exome sequencing
laminopathy
LMNA
biomarkers
troponin T
NT-proBNP
malignant ventricular arrhythmia
arrhythmic risk stratification
DNA methylation
alternative splicing
epigenetics
nonischemic dilated cardiomyopathy
cardiac magnetic resonance imaging
late gadolinium enhancement
long axis strain
left ventricle sphericity index
major adverse cardiovascular events
sex differences
left ventricular reverse remodelling
long-term outcomes
left ventricle non-compaction cardiomyopathy
cardiac magnetic resonance
titin
RNA binding motif protein 20 (RBM20)
sarcomere
diastolic dysfunction
phosphorylation
non-sense mRNA decay
mammalian target of rapamycin (mTOR) complex-1
duchenne muscular distrophy
n/a
thema EDItEUR::M Medicine and Nursing
Dostęp online:ONIX_20210501_9783039437610_26
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