Výsledky vyhledávání - "Skeletal muscle weakness"

Akademický článek

Optimized progression of Full-Body In-Bed Gym workout: an educational case report

Autor: Barbara Ravara, Walter Giuriati, Maria Chiara Maccarone, Helmut Kern, Stefano Masiero, Ugo Carraro

Publikováno v: European Journal of Translational Myology (2023)

People suffering from fatigue syndromes spend less time exercising each day, thus aggravating their motor difficulties. Indeed, muscles and mobility deteriorate with age, while exercising muscles is the only sure countermeasure. It is useful to offer

Externí odkaz: https://doaj.org/article/735a9e9b6d1f4c0f962e6ef2a04e9bb2

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Akademický článek

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Akademický článek

To contrast and reverse skeletal muscle weakness by Full-Body In-Bed Gym in chronic COVID-19 pandemic syndrome

Autor: Ugo Carraro, Giovanna Albertin, Alessandro Martini, Walter Giuriati, Diego Guidolin, Stefano Masiero, Helmut Kern, Christian Hofer, Andrea Marcante, Barbara Ravara

Publikováno v: European Journal of Translational Myology (2021)

Mobility-impaired persons, either very old or younger but suffering with systemic neuromuscular disorders or chronic organ failures, spend small amounts of time for daily physical activity, contributing to aggravate their poor mobility by resting mus

Externí odkaz: https://doaj.org/article/161f9359cfca4519adf860ac6b69e7e2

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Prevalence of sarcopenia in older women with pelvic floor dysfunction

Autor: Rávida da Rocha Lima Silva, Rachel Gabriel Bastos Barbosa, José Ananias Vasconcelos Neto, Janaína Fonseca Victor Coutinho, Marília Braga Marques, Juliana Cunha Maia, Camila Teixeira Moreira Vasconcelos, Dayana Maia Saboia

Publikováno v: European Journal of Obstetrics & Gynecology and Reproductive Biology. 263:159-163

Background Sarcopenia is a determinant of age-related skeletal muscle weakness. In this sense, it is believed that there may be a pathophysiological association between pelvic floor dysfunction (PFD) and sarcopenia; however, few articles investigatin

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c29354f6c5516f671ff13133bce5cf9c
https://doi.org/10.1016/j.ejogrb.2021.06.037

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Emery-Dreifuss muscular dystrophy with dilated cardiomyopathy preceding skeletal muscle symptoms

Autor: Hideaki Ueda, Ki-Sung Kim, Koichi Takamizawa

Publikováno v: Cardiology in the Young. 32:1175-1177

Emery-Dreifuss muscular dystrophy is a slowly progressive skeletal muscle and joint disorder associated with cardiac complications. Dilated cardiomyopathy was the initial manifestation of Emery-Dreifuss muscular dystrophy in an 8-year-old girl. Despi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a261e30337f245dbd6342bcdc3cfea7
https://doi.org/10.1017/s1047951121004674

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Using nuclear envelope mutations to explore age-related skeletal muscle weakness

Autor: Julien Ochala, Edmund Battey, Matthew J. Stroud

Publikováno v: Clinical Science (London, England : 1979)
Battey, E, Stroud, M J & Ochala, J 2020, ' Using nuclear envelope mutations to explore age-related skeletal muscle weakness ', Clinical Science, vol. 134, no. 16, pp. 2177-2187 . https://doi.org/10.1042/CS20190066

Skeletal muscle weakness is an important determinant of age-related declines in independence and quality of life but its causes remain unclear. Accelerated ageing syndromes such as Hutchinson–Gilford Progerin Syndrome, caused by mutations in genes

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f90c23ff89b0c60aa9dc13305c49852b
http://europepmc.org/articles/PMC7450176

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Skeletal muscle weakness and mitochondrial dysfunction in the osteogenesis imperfecta murine (oim) model

Autor: Victoria L. Gremminger

Osteogenesis imperfecta (OI), also commonly referred to as brittle bone disease, is a heritable connective tissue disorder occurring in roughly 1:15,000 births. OI arises as a result of mutations in the type I collagen genes, COL1A1 and COL1A2, appro

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::259e453dab3070ce70471658430cb478
https://doi.org/10.32469/10355/85774

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Thyroid Hormone Receptor α Regulates Autophagy, Mitochondrial Biogenesis, and Fatty Acid Use in Skeletal Muscle

Autor: Xuguang Zhu, Rohit A. Sinha, Jia Pei Ho, Paul M. Yen, Cho Rong Han, Karine Gauthier, Sheue-yann Cheng, Andrea Lim, Jin Zhou

Publikováno v: Endocrinology
Endocrinology, 2021, 162 (9), ⟨10.1210/endocr/bqab112⟩
Endocrinology, Endocrine Society, 2021, 162 (9), ⟨10.1210/endocr/bqab112⟩

Skeletal muscle (SM) weakness occurs in hypothyroidism and resistance to thyroid hormone α (RTHα) syndrome. However, the cell signaling and molecular mechanism(s) underlying muscle weakness under these conditions is not well understood. We thus exa

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e473ccb3ae8d0e9b9d86e615b07c0215
https://hal.science/hal-03403597

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