"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 |
|---|
| 1993 | 1 | 0 | 1 |
| 2003 | 1 | 0 | 1 |
| 2004 | 1 | 0 | 1 |
| 2005 | 1 | 0 | 1 |
| 2006 | 0 | 4 | 4 |
| 2007 | 2 | 0 | 2 |
| 2008 | 1 | 0 | 1 |
| 2009 | 1 | 0 | 1 |
| 2011 | 1 | 1 | 2 |
| 2012 | 1 | 0 | 1 |
| 2013 | 3 | 0 | 3 |
| 2014 | 1 | 1 | 2 |
| 2015 | 2 | 2 | 4 |
| 2016 | 1 | 0 | 1 |
| 2017 | 1 | 0 | 1 |
| 2018 | 2 | 0 | 2 |
| 2019 | 2 | 1 | 3 |
| 2020 | 1 | 0 | 1 |
| 2022 | 1 | 0 | 1 |
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Below are the most recent publications written about "Muscular Diseases" by people in Profiles.
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Dengue infection triggered immune mediated necrotizing myopathy in children: a case report and literature review. Pediatr Rheumatol Online J. 2022 Jun 07; 20(1):40.
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Excessive Dynamic Airway Collapse in Asthma and COPD: Physiologic Epiphenomenon or Steroid-Induced Myopathy? Chest. 2020 12; 158(6):2695-2696.
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Pancreatic Malnutrition in Children. Pediatr Ann. 2019 Nov 01; 48(11):e441-e447.
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Genetic regulatory variation in populations informs transcriptome analysis in rare disease. Science. 2019 10 18; 366(6463):351-356.
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Novel COL12A1 variant as a cause of mild familial extracellular matrix-related myopathy. Clin Genet. 2019 06; 95(6):736-738.
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Myopathy associated BAG3 mutations lead to protein aggregation by stalling Hsp70 networks. Nat Commun. 2018 12 17; 9(1):5342.
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A pattern-based approach to the interpretation of skeletal muscle biopsies. Mod Pathol. 2019 04; 32(4):462-483.
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Persistent Safety and Efficacy of Evolocumab in Patients with Statin Intolerance: a Subset Analysis of the OSLER Open-Label Extension Studies. Cardiovasc Drugs Ther. 2018 08; 32(4):365-372.
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Development and Content Validity of the Statin Experience Assessment Questionnaire (SEAQ)?. Patient. 2017 06; 10(3):321-334.
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Neuromuscular Blocking Agents and Neuromuscular Dysfunction Acquired in Critical Illness: A Systematic Review and Meta-Analysis. Crit Care Med. 2016 Nov; 44(11):2070-2078.