"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 |
|---|
| 2001 | 1 | 0 | 1 |
| 2003 | 1 | 1 | 2 |
| 2004 | 1 | 0 | 1 |
| 2010 | 0 | 1 | 1 |
| 2012 | 0 | 1 | 1 |
| 2013 | 1 | 0 | 1 |
| 2015 | 1 | 0 | 1 |
| 2016 | 1 | 0 | 1 |
| 2019 | 0 | 1 | 1 |
| 2020 | 2 | 0 | 2 |
| 2021 | 2 | 0 | 2 |
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Below are the most recent publications written about "Muscular Diseases" by people in Profiles.
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Haematological characteristics and spontaneous haematological recovery in Pearson syndrome. Br J Haematol. 2021 06; 193(6):1283-1287.
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Clinical and genetic characterization of PYROXD1-related myopathy patients from Turkey. Am J Med Genet A. 2021 06; 185(6):1678-1690.
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Loss of supervillin causes myopathy with myofibrillar disorganization and autophagic vacuoles. Brain. 2020 08 01; 143(8):2406-2420.
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Differential diagnosis of vacuolar myopathies in the NGS era. Brain Pathol. 2020 09; 30(5):877-896.
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The genomic and clinical landscape of fetal akinesia. Genet Med. 2020 03; 22(3):511-523.
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Mutant desmin substantially perturbs mitochondrial morphology, function and maintenance in skeletal muscle tissue. Acta Neuropathol. 2016 09; 132(3):453-73.
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A specific IFIH1 gain-of-function mutation causes Singleton-Merten syndrome. Am J Hum Genet. 2015 Feb 05; 96(2):275-82.
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Recessive TRAPPC11 mutations cause a disease spectrum of limb girdle muscular dystrophy and myopathy with movement disorder and intellectual disability. Am J Hum Genet. 2013 Jul 11; 93(1):181-90.
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A novel mtDNA large-scale mutation clinically exclusively presenting with refractory anemia: is there a chance to predict disease progression? J Pediatr Hematol Oncol. 2012 May; 34(4):283-92.
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POLG mutations cause decreased mitochondrial DNA repopulation rates following induced depletion in human fibroblasts. Biochim Biophys Acta. 2011 Mar; 1812(3):321-5.
MeSH information
