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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1966 1
1968 1
1969 1
1971 4
1972 4
1973 3
1974 5
1975 2
1976 7
1977 6
1978 3
1979 3
1980 5
1981 4
1982 5
1983 5
1984 4
1985 7
1986 8
1987 6
1988 14
1989 13
1990 11
1991 21
1992 15
1993 27
1994 28
1995 25
1996 37
1997 33
1998 57
1999 37
2000 52
2001 38
2002 33
2003 37
2004 31
2005 51
2006 46
2007 41
2008 46
2009 41
2010 55
2011 66
2012 56
2013 63
2014 66
2015 62
2016 43
2017 51
2018 47
2019 50
2020 47
2021 34
2022 18
2023 16
2024 4

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1,389 results

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Page 1
Skeletal muscle atrophy: From mechanisms to treatments.
Yin L, Li N, Jia W, Wang N, Liang M, Yang X, Du G. Yin L, et al. Pharmacol Res. 2021 Oct;172:105807. doi: 10.1016/j.phrs.2021.105807. Epub 2021 Aug 10. Pharmacol Res. 2021. PMID: 34389456 Review.
Skeletal muscle is a crucial tissue for movement, gestural assistance, metabolic homeostasis, and thermogenesis. ...In this paper, the mechanisms and treatment strategies for skeletal muscle atrophy are briefly reviewed....
Skeletal muscle is a crucial tissue for movement, gestural assistance, metabolic homeostasis, and thermogenesis. ...In this pa …
Congenital myopathies: an update.
Claeys KG. Claeys KG. Dev Med Child Neurol. 2020 Mar;62(3):297-302. doi: 10.1111/dmcn.14365. Epub 2019 Oct 2. Dev Med Child Neurol. 2020. PMID: 31578728 Free article. Review.
Congenital myopathies comprise a clinical, histopathological, and genetic heterogeneous group of rare hereditary muscle diseases that are defined by architectural abnormalities in the muscle fibres. ...Besides the clinical features, muscle biops …
Congenital myopathies comprise a clinical, histopathological, and genetic heterogeneous group of rare hereditary muscle diseas …
Emery-Dreifuss muscular dystrophy.
Heller SA, Shih R, Kalra R, Kang PB. Heller SA, et al. Muscle Nerve. 2020 Apr;61(4):436-448. doi: 10.1002/mus.26782. Epub 2019 Dec 28. Muscle Nerve. 2020. PMID: 31840275 Free PMC article. Review.
Emery-Dreifuss muscular dystrophy (EDMD) is a rare muscular dystrophy, but is particularly important to diagnose due to frequent life-threatening cardiac complications. EDMD classically presents with muscle weakness, early contractures, cardiac conduction abnormalities …
Emery-Dreifuss muscular dystrophy (EDMD) is a rare muscular dystrophy, but is particularly important to diagnose due to frequent life-threat …
Muscle ultrasound: Present state and future opportunities.
Wijntjes J, van Alfen N. Wijntjes J, et al. Muscle Nerve. 2021 Apr;63(4):455-466. doi: 10.1002/mus.27081. Epub 2020 Oct 13. Muscle Nerve. 2021. PMID: 33051891 Free PMC article. Review.
In addition, more information should be collected on the relation between specific neuromuscular disorders, disease stages, and expected ultrasound abnormalities, as this will enhance specificity of the technique and enable the use of muscle ultrasound as a biomarke …
In addition, more information should be collected on the relation between specific neuromuscular disorders, disease stages, and expected ult …
Skeletal muscle aging: influence of oxidative stress and physical exercise.
Gomes MJ, Martinez PF, Pagan LU, Damatto RL, Cezar MDM, Lima ARR, Okoshi K, Okoshi MP. Gomes MJ, et al. Oncotarget. 2017 Mar 21;8(12):20428-20440. doi: 10.18632/oncotarget.14670. Oncotarget. 2017. PMID: 28099900 Free PMC article. Review.
Skeletal muscle abnormalities are responsible for significant disability in the elderly. ...There has been an increase in information on signaling pathways beneficially modulated by exercise; nonetheless, studies are needed to establish the best type, intensi …
Skeletal muscle abnormalities are responsible for significant disability in the elderly. ...There has been an increase …
Mitochondrial Disorder: Kearns-Sayre Syndrome.
Tsang SH, Aycinena ARP, Sharma T. Tsang SH, et al. Adv Exp Med Biol. 2018;1085:161-162. doi: 10.1007/978-3-319-95046-4_30. Adv Exp Med Biol. 2018. PMID: 30578503 Review.
Mitochondrial diseases are multisystem disorders: anemia, myopathy, lactic acidosis, CNS abnormality, endocrine abnormalities, renal disease, sensorineural deafness, and retinal involvement. ...Full-field ERG does show evidence of generalized retinal dysfunction, in …
Mitochondrial diseases are multisystem disorders: anemia, myopathy, lactic acidosis, CNS abnormality, endocrine abnormalities, …
Pathophysiology and mechanisms of primary sarcopenia (Review).
Nishikawa H, Fukunishi S, Asai A, Yokohama K, Nishiguchi S, Higuchi K. Nishikawa H, et al. Int J Mol Med. 2021 Aug;48(2):156. doi: 10.3892/ijmm.2021.4989. Epub 2021 Jun 29. Int J Mol Med. 2021. PMID: 34184088 Review.
Aging causes skeletal muscle atrophy, and myofiber loss can be a critical component of this process. ...In addition, mitochondrial dysfunction causes metabolic abnormalities, such as insulin resistance, which may lead to quantitative and qualitative abnorm …
Aging causes skeletal muscle atrophy, and myofiber loss can be a critical component of this process. ...In addition, mitochond …
Sarcopenia in cirrhosis: from pathogenesis to interventions.
Ebadi M, Bhanji RA, Mazurak VC, Montano-Loza AJ. Ebadi M, et al. J Gastroenterol. 2019 Oct;54(10):845-859. doi: 10.1007/s00535-019-01605-6. Epub 2019 Aug 7. J Gastroenterol. 2019. PMID: 31392488 Free PMC article. Review.
Sarcopenia (severe muscle depletion) is a prevalent muscle abnormality in patients with cirrhosis that confers poor prognosis both pre- and post-liver transplantation. ...A favored atrophy of type II fast-twitch glycolytic fibers seems to occur in patients wi …
Sarcopenia (severe muscle depletion) is a prevalent muscle abnormality in patients with cirrhosis that confers poor pro …
Imaging of the diaphragm: anatomy and function.
Nason LK, Walker CM, McNeeley MF, Burivong W, Fligner CL, Godwin JD. Nason LK, et al. Radiographics. 2012 Mar-Apr;32(2):E51-70. doi: 10.1148/rg.322115127. Radiographics. 2012. PMID: 22411950 Review.
The diaphragm is the primary muscle of ventilation. Dysfunction of the diaphragm is an underappreciated cause of respiratory difficulties and may be due to a wide variety of entities, including surgery, trauma, tumor, and infection. ...Diaphragmatic weakness is indicated b …
The diaphragm is the primary muscle of ventilation. Dysfunction of the diaphragm is an underappreciated cause of respiratory difficul …
Mitochondrial Dysfunction in Heart Failure With Preserved Ejection Fraction.
Kumar AA, Kelly DP, Chirinos JA. Kumar AA, et al. Circulation. 2019 Mar 12;139(11):1435-1450. doi: 10.1161/CIRCULATIONAHA.118.036259. Circulation. 2019. PMID: 30856000 Free PMC article. Review.
Exercise intolerance is the hallmark of HFpEF and appears to be caused by both cardiac and peripheral abnormalities in the arterial tree and skeletal muscle. Mitochondrial abnormalities can significantly contribute to impaired oxygen utilization and th …
Exercise intolerance is the hallmark of HFpEF and appears to be caused by both cardiac and peripheral abnormalities in the arterial t …
1,389 results