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Comorbidities in Chronic Kidney Disease (CKD)
| Comorbidities in Chronic Kidney Disease (CKD) |
| Autore | Jankowski Joachim |
| Pubbl/distr/stampa | Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021 |
| Descrizione fisica | 1 online resource (184 p.) |
| Soggetto topico | Medicine and Nursing |
| Soggetto non controllato |
ageing
arterial calcification arterial stiffness bone calcification cardiac fibrosis cardiorenal syndrome cardiovascular cardiovascular disease carotid-femoral pulse wave velocity chronic kidney disease chronodisruption chronodisruptor circadian rhythm CKD CKD-MBD coagulation comorbidity end-stage kidney disease endothelial dysfunction epigenetics experimental rodent models FGF23 FGFG23 fibrosis gut heart failure hemodialysis inflammation internal clock klotho Klotho left ventricular hypertrophy left-ventricular hypertrophy lipid metabolism organ crosstalk p-cresyl sulfate parathyroid hormone phosphate premature ageing PTH sclerostin secondary hyperparathyroidism senescence uremia uremic cardiomyopathy uremic cardiopathy uremic toxin uremic toxins vascular calcification Wnt/β-catenin |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Altri titoli varianti | Comorbidities in Chronic Kidney Disease |
| Record Nr. | UNINA-9910557705903321 |
Jankowski Joachim
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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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Role of Genomics in the Management of Hypertension
| Role of Genomics in the Management of Hypertension |
| Autore | Mulatero Paolo |
| Pubbl/distr/stampa | Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020 |
| Descrizione fisica | 1 online resource (200 p.) |
| Soggetto topico |
Biology, life sciences
Research & information: general |
| Soggetto non controllato |
adducin
African American aldosterone aldosterone-producing adenoma ARMC5 atrial natriuretic peptide blood pressure burden test CACNA1D cardiac hypertrophy cardio-tonic steroids cardiovascular diseases cervical artery dissection CRY1 CRY2 DNA methylation endocrine hypertension endogenous ouabain endothelial cells endothelial dysfunction epigenetics essential hypertension exome microarray fibromuscular dysplasia genetic association genetics genetics of left ventricular hypertrophy genome-wide association studies GRK4 heart failure histone modifications HSD3B1 HSD3B2 hypertension hypokalemia Kruppel-like factor 15 left ventricular hypertrophy Liddle syndrome low renin hypertension low-renin micro RNA mineralocorticoid receptor monogenic hypertension next-generation sequencing non atherosclerotic vascular stenosis non-coding RNA PHACTR1 platelet aggregation primary aldosteronism rare variants rare-variants association testing renal damage renin SCNN1A SCNN1B SCNN1G sequence kernel association test smooth muscle cells contraction spontaneous coronary arteries dissection T2238C variant transcriptome profiing vascular smooth muscle cells |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910557741603321 |
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Mulatero Paolo
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| Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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