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Biomarkers and Nutrients in Musculoskeletal Disorders
| Biomarkers and Nutrients in Musculoskeletal Disorders |
| Autore | Calvo-Lobo César |
| Pubbl/distr/stampa | Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022 |
| Descrizione fisica | 1 online resource (120 p.) |
| Soggetto topico |
Humanities
Social interaction |
| Soggetto non controllato |
activated satellite cells
acute sedentary lifestyle biomarkers bone density bowel diseases COVID-19 diet dystrophy markers electromyography glutathione high-fat diet insulin resistance l-cysteine metabolic consequences metabolic syndrome metabolomics muscle progenitor cells muscle regeneration markers muscle reloading muscle unloading myofascial pain syndrome myogenic markers n/a nutrients nutrition obesity osteoporosis positive energy balance quiescent satellite cells sarcopenia sirtuin-1 skeletal muscle spinal muscular atrophy spontaneous neurotransmission step reduction therapeutics vitamin D deficiency |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910557608803321 |
Calvo-Lobo César
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| Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Neuromuscular Disorders in Children and Adolescents
| Neuromuscular Disorders in Children and Adolescents |
| Autore | Korinthenberg Rudolf |
| Pubbl/distr/stampa | Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022 |
| Descrizione fisica | 1 online resource (146 p.) |
| Soggetto topico |
Medicine and Nursing
Neurology and clinical neurophysiology |
| Soggetto non controllato |
3-hydroxy-3-methylglutaryl
adolescents AMC brachial plexus neuritis carpal tunnel syndrome carrier frequency chaperone-assisted autophagy Charcot-Marie-Tooth disease child neurology children clinical course clinical trials coenzyme A reductase contractures distal arthrogryposis Duchenne muscular dystrophy ECEL1 electrodiagnostic studies fine manual dexterity GAA gene general population database genetic prevalence hereditary sensory and motor neuropathy inflammatory neuropathy juvenile myositis kyphosis median nerve neuropathy metabolic neuropathy mucopolysaccharidosis muscle muscle MRI n/a neuromuscular neuromuscular disease neuromuscular ultrasound neuropathy nusinersen paralysis patient-reported outcomes pediatrics Pompe disease posterior spinal fusion public health surveillance quality of life sagittal plane deformity signal recognition particle spinal muscular atrophy spinal muscular atrophy (SMA) therapy traumatic neuropathy ultrasonographic elastography vaccination |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910566465903321 |
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Korinthenberg Rudolf
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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 |
| Soggetto non controllato |
-omics approaches
AAV adult patients ALS ALS genes ALS pathology ALS variants Amyotrophic Lateral Sclerosis autophagy axonal transport Becker muscular dystrophy becker muscular dystrophy (BMD) biomarkers calprotectin Canadian Neuromuscular Disease Registry clinical trials comparative genomic hybridization array (CGH) corticosteroids CRISPR-Cas9 D4Z4 deflazacort disease heterogeneity disease models disease modifiers DMARD DMD Duchenne muscular dystrophy duchenne muscular dystrophy (DMD) Duchenne muscular dystrophy (DMD) DUX4 dystrophin dystrophinopathy dystrophy Emery-Dreifuss muscular dystrophy endocytosis epigenetic changes eteplirsen excitotoxicity exon skipping exon skipping therapy exon-skipping therapies facioscapulohumeral dystrophy FSHD functional outcomes gene editing gene prioritization gene therapy genetic neuromuscular disorders genome-wide association studies genomics genotype-phenotype genotype-phenotype correlations glucocorticoids golodirsen GWAS LMNA machine learning methotrexate miRNA mitochondria dysfunction MND multiple logistic regression analysis multiplex ligation probe amplification (MLPA) multiplex polymerase chain reaction (PCR) muscle n/a neuromuscular diseases next-generation sequencing (NGS) Nusinersen Omics oxidative stress pharmacodynamic biomarkers pharmacogenomics polyadenylation precision medicine prednisone proteomics reading frame rule regulation rheumatoid arthritis RNA metabolism safety Sanger sequencing secretion skip-equivalent deletions SMA SNP spinal muscular atrophy TALEN toxicity transcription translational research viltolarsen XLMTM |
| 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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