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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 electronic resource (120 p.) |
| Soggetto topico |
Humanities
Social interaction |
| Soggetto non controllato |
COVID-19
acute sedentary lifestyle step reduction positive energy balance metabolic consequences insulin resistance metabolic syndrome sarcopenia bowel diseases diet osteoporosis bone density nutrients muscle unloading muscle reloading sirtuin-1 muscle progenitor cells activated satellite cells quiescent satellite cells muscle regeneration markers electromyography high-fat diet myofascial pain syndrome obesity spontaneous neurotransmission vitamin D deficiency l-cysteine glutathione myogenic markers dystrophy markers skeletal muscle spinal muscular atrophy metabolomics nutrition therapeutics biomarkers |
| 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 electronic resource (146 p.) |
| Soggetto topico |
Medicine
Neurology & clinical neurophysiology |
| Soggetto non controllato |
Pompe disease
GAA gene general population database carrier frequency genetic prevalence spinal muscular atrophy quality of life child neurology patient-reported outcomes neuromuscular carpal tunnel syndrome median nerve neuropathy electrodiagnostic studies neuromuscular ultrasound mucopolysaccharidosis neuropathy children adolescents Charcot-Marie-Tooth disease traumatic neuropathy inflammatory neuropathy metabolic neuropathy posterior spinal fusion kyphosis sagittal plane deformity signal recognition particle 3-hydroxy-3-methylglutaryl coenzyme A reductase juvenile myositis therapy clinical course chaperone-assisted autophagy clinical trials Duchenne muscular dystrophy public health surveillance distal arthrogryposis AMC ECEL1 contractures muscle MRI spinal muscular atrophy (SMA) nusinersen fine manual dexterity ultrasonographic elastography neuromuscular disease muscle brachial plexus neuritis hereditary sensory and motor neuropathy paralysis vaccination pediatrics |
| 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 electronic resource (318 p.) |
| Soggetto topico | Research & information: general |
| Soggetto non controllato |
LMNA
Emery-Dreifuss muscular dystrophy Omics ALS MND ALS variants genotype-phenotype ALS genes FSHD DUX4 transcription muscle regulation spinal muscular atrophy adult patients disease heterogeneity Nusinersen disease modifiers functional outcomes biomarkers epigenetic changes -omics approaches oxidative stress mitochondria dysfunction axonal transport autophagy endocytosis secretion excitotoxicity RNA metabolism Duchenne muscular dystrophy (DMD) exon-skipping therapies next-generation sequencing (NGS) Sanger sequencing multiplex ligation probe amplification (MLPA) multiplex polymerase chain reaction (PCR) comparative genomic hybridization array (CGH) viltolarsen eteplirsen golodirsen rheumatoid arthritis SNP DMARD methotrexate pharmacogenomics Duchenne muscular dystrophy pharmacodynamic biomarkers prednisone deflazacort glucocorticoids corticosteroids safety neuromuscular diseases translational research disease models precision medicine miRNA proteomics calprotectin dystrophy Becker muscular dystrophy dystrophinopathy genotype-phenotype correlations Canadian Neuromuscular Disease Registry reading frame rule dystrophin multiple logistic regression analysis exon skipping therapy Amyotrophic Lateral Sclerosis machine learning genome-wide association studies GWAS genomics ALS pathology gene prioritization AAV genetic neuromuscular disorders gene therapy clinical trials toxicity SMA DMD XLMTM facioscapulohumeral dystrophy TALEN CRISPR-Cas9 gene editing polyadenylation D4Z4 duchenne muscular dystrophy (DMD) becker muscular dystrophy (BMD) exon skipping skip-equivalent deletions |
| 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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