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Characterization and Clinical Management of Dilated Cardiomyopathy
| Characterization and Clinical Management of Dilated Cardiomyopathy |
| Autore | Merlo Marco |
| Pubbl/distr/stampa | Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021 |
| Descrizione fisica | 1 online resource (232 p.) |
| Soggetto topico | Medicine |
| Soggetto non controllato |
alternative splicing
arrhythmias arrhythmic risk stratification atrial fibrillation biomarkers calcium cardiac channelopathy cardiac magnetic resonance cardiac magnetic resonance imaging cardiac resynchronization therapy cardiac sodium channel cardiomyopathy congenital heart disease congestive heart failure desmin diastolic dysfunction dilated cardiomyopathy DNA methylation duchenne muscular distrophy epigenetics gene therapy genetics heart heart failure laminopathy late gadolinium enhancement left atrial strain left ventricle non-compaction cardiomyopathy left ventricle sphericity index left ventricular noncompaction left ventricular reverse remodelling LMNA long axis strain long-term outcomes major adverse cardiovascular events malignant ventricular arrhythmia mammalian target of rapamycin (mTOR) complex-1 mdx membrane stabilization mitochondrial dysfunction muscular dystrophy myopathy n/a non-ischemic cardiomyopathy non-sense mRNA decay nonischemic dilated cardiomyopathy NT-proBNP oxidative stress phospholamban phosphorylation precision medicine RNA binding motif protein 20 (RBM20) sarcomere SCN5A Serca2a sex differences supraventricular arrhythmia systolic dysfunction tachycardiomyopathy titin troponin T ventricular arrhythmia whole exome sequencing |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910557595503321 |
Merlo Marco
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| Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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JCM-Advances in Cardiology
| JCM-Advances in Cardiology |
| Autore | Henein Michael |
| Pubbl/distr/stampa | Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022 |
| Descrizione fisica | 1 online resource (118 p.) |
| Soggetto topico |
Medicine and Nursing
Pharmacology |
| Soggetto non controllato |
ACE2
adipokines adiponectin arrhythmias cardiovascular disease cardiovascular risk factors Coptic clergy COVID-19 CRT dilated cardiomyopathy (DCM) extraction hepatic steatosis Holter ECG ICD implantable cardioverter defibrillator implantable loop recorder lamin A lamin C LMNA major adverse events metabolic-dysfunction-associated fatty liver disease (MAFLD) mortality myocarditis n/a next generation sequencing (NGS) obesity pacing prevalence primary percutaneous intervention reimplantation renin-angiotensin system ST segment elevation myocardial infarction SteatoTest telemonitoring visfatin |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910566459203321 |
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Henein Michael
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| Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Understanding Neuromuscular Health and Disease: Advances in Genetics, Omics, and Molecular Function
| Understanding Neuromuscular Health and Disease: Advances in Genetics, Omics, and Molecular Function |
| Autore | Duddy William |
| Pubbl/distr/stampa | Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021 |
| Descrizione fisica | 1 online resource (318 p.) |
| Soggetto topico |
Research & information: general
Research and information: general |
| Soggetto non controllato |
-omics approaches
adult patients autophagy axonal transport becker muscular dystrophy (BMD) biomarkers calprotectin clinical trials comparative genomic hybridization array (CGH) corticosteroids deflazacort disease heterogeneity disease models disease modifiers duchenne muscular dystrophy (DMD) dystrophin dystrophinopathy dystrophy endocytosis epigenetic changes eteplirsen excitotoxicity exon skipping exon skipping therapy exon-skipping therapies facioscapulohumeral dystrophy functional outcomes gene editing gene prioritization gene therapy genetic neuromuscular disorders genome-wide association studies genomics genotype-phenotype genotype-phenotype correlations glucocorticoids golodirsen machine learning methotrexate miRNA mitochondria dysfunction multiple logistic regression analysis multiplex ligation probe amplification (MLPA) multiplex polymerase chain reaction (PCR) muscle neuromuscular diseases next-generation sequencing (NGS) oxidative stress pharmacodynamic biomarkers pharmacogenomics polyadenylation precision medicine prednisone proteomics reading frame rule regulation rheumatoid arthritis safety secretion skip-equivalent deletions spinal muscular atrophy toxicity transcription translational research viltolarsen AAV ALS genes ALS pathology ALS variants Amyotrophic Lateral Sclerosis Becker muscular dystrophy Canadian Neuromuscular Disease Registry CRISPR-Cas9 D4Z4 DMARD DMD Duchenne muscular dystrophy Duchenne muscular dystrophy (DMD) DUX4 Emery-Dreifuss muscular dystrophy FSHD GWAS LMNA MND Nusinersen Omics RNA metabolism Sanger sequencing SMA SNP TALEN XLMTM |
| ISBN |
9783036516226
9783036516219 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Altri titoli varianti | Understanding Neuromuscular Health and Disease |
| Record Nr. | UNINA-9910557669103321 |
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Duddy William
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| Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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