"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 |
|---|
| 1997 | 1 | 1 | 2 |
| 2000 | 1 | 0 | 1 |
| 2001 | 1 | 0 | 1 |
| 2003 | 1 | 0 | 1 |
| 2004 | 1 | 0 | 1 |
| 2005 | 0 | 1 | 1 |
| 2006 | 2 | 0 | 2 |
| 2007 | 1 | 1 | 2 |
| 2008 | 2 | 2 | 4 |
| 2009 | 1 | 0 | 1 |
| 2010 | 1 | 0 | 1 |
| 2011 | 2 | 0 | 2 |
| 2012 | 1 | 0 | 1 |
| 2013 | 3 | 0 | 3 |
| 2014 | 2 | 2 | 4 |
| 2015 | 4 | 2 | 6 |
| 2016 | 2 | 2 | 4 |
| 2017 | 2 | 2 | 4 |
| 2018 | 3 | 1 | 4 |
| 2020 | 2 | 2 | 4 |
| 2021 | 2 | 0 | 2 |
| 2022 | 4 | 0 | 4 |
| 2023 | 6 | 2 | 8 |
| 2024 | 1 | 2 | 3 |
| 2025 | 2 | 1 | 3 |
| 2026 | 3 | 0 | 3 |
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Below are the most recent publications written about "Muscular Diseases" by people in Profiles.
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Multimodal Noninvasive Biomarker Characterization of Structural and Functional Alterations in ADSS1-Deficient Myopathy. J Inherit Metab Dis. 2026 May; 49(3):e70193.
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International Forum on Visceral Myopathy 2024: Advances in the Knowledge of the Disease. Neurogastroenterol Motil. 2026 Apr; 38(4):e70317.
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Outcomes of kidney transplantation in three patients with single large-scale mitochondrial DNA deletion syndromes. Mol Genet Metab. 2026 Mar; 147(3):109731.
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Lethal Sycamore maple intoxication in a grazing three-month-old foal. J Equine Vet Sci. 2025 Dec; 155:105713.
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Detecting mitochondrial electron transport chain enzyme defects in low-heteroplasmy single large-scale mtDNA deletion syndromes (SLSMDSs). Mol Genet Metab. 2025 Nov; 146(3):109260.
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Alternative splicing of the Snap23 microexon is regulated by MBNL, QKI, and RBFOX2 in a tissue-specific manner and is altered in striated muscle diseases. RNA Biol. 2025 12; 22(1):1-20.
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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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ER stress and ERO1: Potential therapeutic targets for inherited myopathies. Cell Rep Med. 2024 Mar 19; 5(3):101462.
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Postsynaptic ?1?spectrin maintains Na+ channels at the neuromuscular junction. J Physiol. 2024 03; 602(6):1127-1145.
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Stakeholder endorsement advancing the implementation of a patient-reported domain for harms in rheumatology clinical trials: Outcome of the OMERACT Safety Working Group. Semin Arthritis Rheum. 2023 12; 63:152288.