"Muscular Diseases" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Acquired, familial, and congenital disorders of SKELETAL MUSCLE and SMOOTH MUSCLE.
| Descriptor ID |
D009135
|
| MeSH Number(s) |
C05.651 C10.668.491
|
| Concept/Terms |
Muscular Diseases- Muscular Diseases
- Muscular Disease
- Myopathies
- Myopathy
- Muscle Disorders
- Muscle Disorder
- Myopathic Conditions
- Myopathic Condition
|
Below are MeSH descriptors whose meaning is more general than "Muscular Diseases".
Below are MeSH descriptors whose meaning is more specific than "Muscular Diseases".
This graph shows the total number of publications written about "Muscular Diseases" by people in this website by year, and whether "Muscular Diseases" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1994 | 3 | 3 | 6 |
| 1995 | 3 | 1 | 4 |
| 1996 | 0 | 1 | 1 |
| 1997 | 1 | 2 | 3 |
| 1999 | 1 | 0 | 1 |
| 2000 | 2 | 3 | 5 |
| 2001 | 1 | 1 | 2 |
| 2003 | 1 | 2 | 3 |
| 2004 | 5 | 0 | 5 |
| 2005 | 1 | 1 | 2 |
| 2006 | 4 | 0 | 4 |
| 2007 | 1 | 1 | 2 |
| 2008 | 2 | 3 | 5 |
| 2009 | 1 | 0 | 1 |
| 2010 | 1 | 0 | 1 |
| 2011 | 2 | 0 | 2 |
| 2012 | 2 | 1 | 3 |
| 2013 | 3 | 0 | 3 |
| 2014 | 2 | 4 | 6 |
| 2015 | 4 | 2 | 6 |
| 2016 | 1 | 2 | 3 |
| 2017 | 3 | 2 | 5 |
| 2018 | 4 | 1 | 5 |
| 2020 | 2 | 1 | 3 |
| 2021 | 1 | 0 | 1 |
| 2022 | 3 | 0 | 3 |
| 2023 | 1 | 0 | 1 |
| 2024 | 0 | 2 | 2 |
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Below are the most recent publications written about "Muscular Diseases" by people in Profiles.
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Myosteatosis Is Associated With Frailty and Poor Physical Function in Patients Undergoing Liver Transplant Evaluation: A Cohort Study. Clin Transplant. 2024 Dec; 38(12):e70034.
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Postsynaptic ?1?spectrin maintains Na+ channels at the neuromuscular junction. J Physiol. 2024 Mar; 602(6):1127-1145.
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Bi-allelic variants in HMGCR cause an autosomal-recessive progressive limb-girdle muscular dystrophy. Am J Hum Genet. 2023 06 01; 110(6):989-997.
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Statin related muscle symptoms: is it time to move on. BMJ. 2022 12 20; 379:o2939.
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A recurrent single-exon deletion in TBCK might be under-recognized in patients with infantile hypotonia and psychomotor delay. Hum Mutat. 2022 12; 43(12):1816-1823.
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Efficacy and safety of bempedoic acid in patients not receiving statins in phase 3 clinical trials. J Clin Lipidol. 2022 May-Jun; 16(3):286-297.
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The role of junctophilin proteins in cellular function. Physiol Rev. 2022 07 01; 102(3):1211-1261.
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Pathological mechanisms of vacuolar aggregate myopathy arising from a Casq1 mutation. FASEB J. 2021 05; 35(5):e21349.
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Effect of Pharmacogenetic Testing for Statin Myopathy Risk vs Usual Care on Blood Cholesterol: A Randomized Clinical Trial. JAMA Netw Open. 2020 12 01; 3(12):e2027092.
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A novel acceptor stem variant in mitochondrial tRNATyr impairs mitochondrial translation and is associated with a severe phenotype. Mol Genet Metab. 2020 12; 131(4):398-404.