"Muscular Atrophy" 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.
Derangement in size and number of muscle fibers occurring with aging, reduction in blood supply, or following immobilization, prolonged weightlessness, malnutrition, and particularly in denervation.
| Descriptor ID |
D009133
|
| MeSH Number(s) |
C10.597.613.612 C23.300.070.500 C23.888.592.608.612
|
| Concept/Terms |
Muscular Atrophy- Muscular Atrophy
- Atrophies, Muscular
- Atrophy, Muscular
- Muscular Atrophies
- Atrophy, Muscle
- Atrophies, Muscle
- Muscle Atrophies
- Muscle Atrophy
Neurogenic Muscular Atrophy- Neurogenic Muscular Atrophy
- Atrophies, Neurogenic Muscular
- Atrophy, Neurogenic Muscular
- Muscular Atrophies, Neurogenic
- Muscular Atrophy, Neurogenic
- Neurogenic Muscular Atrophies
- Neurotrophic Muscular Atrophy
- Atrophies, Neurotrophic Muscular
- Atrophy, Neurotrophic Muscular
- Muscular Atrophies, Neurotrophic
- Muscular Atrophy, Neurotrophic
- Neurotrophic Muscular Atrophies
|
Below are MeSH descriptors whose meaning is more general than "Muscular Atrophy".
Below are MeSH descriptors whose meaning is more specific than "Muscular Atrophy".
This graph shows the total number of publications written about "Muscular Atrophy" by people in this website by year, and whether "Muscular Atrophy" 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 | 0 | 1 | 1 |
| 2001 | 1 | 0 | 1 |
| 2006 | 0 | 1 | 1 |
| 2009 | 0 | 1 | 1 |
| 2012 | 2 | 1 | 3 |
| 2013 | 0 | 2 | 2 |
| 2014 | 1 | 0 | 1 |
| 2015 | 1 | 0 | 1 |
| 2016 | 1 | 0 | 1 |
| 2017 | 2 | 1 | 3 |
| 2018 | 0 | 1 | 1 |
| 2019 | 0 | 1 | 1 |
| 2020 | 2 | 0 | 2 |
| 2021 | 1 | 0 | 1 |
| 2022 | 0 | 1 | 1 |
| 2024 | 1 | 1 | 2 |
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Below are the most recent publications written about "Muscular Atrophy" by people in Profiles.
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Combined Levothyroxine and Propylthiouracil Treatment in Children with Monocarboxylate Transporter 8 Deficiency: A Multicenter Case Series of 12 Patients. Thyroid. 2024 Nov; 34(11):1435-1443.
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Impaired T3 uptake and action in MCT8-deficient cerebral organoids underlie Allan-Herndon-Dudley syndrome. JCI Insight. 2024 Feb 20; 9(7).
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AAV9-MCT8 Delivery at Juvenile Stage Ameliorates Neurological and Behavioral Deficits in a Mouse Model of MCT8-Deficiency. Thyroid. 2022 07; 32(7):849-859.
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Measurement of Reverse Triiodothyronine Level and the Triiodothyronine to Reverse Triiodothyronine Ratio in Dried Blood Spot Samples at Birth May Facilitate Early Detection of Monocarboxylate Transporter 8 Deficiency. Thyroid. 2021 09; 31(9):1316-1321.
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Prenatal Treatment of Thyroid Hormone Cell Membrane Transport Defect Caused by MCT8 Gene Mutation. Thyroid. 2021 05; 31(5):713-720.
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Sorting Variants of Unknown Significance Identified by Whole Exome Sequencing: Genetic and Laboratory Investigations of Two Novel MCT8 Variants. Thyroid. 2020 03; 30(3):463-465.
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Cellular mechanisms promoting cachexia and how they are opposed by sirtuins 1. Can J Physiol Pharmacol. 2019 Apr; 97(4):235-245.
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Effects of the Number of Muscle-Nerve-Muscle Grafts on Rat Facial Nerve Functional Recovery. Ann Otol Rhinol Laryngol. 2018 Nov; 127(11):791-797.
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The histone deacetylase SIRT6 blocks myostatin expression and development of muscle atrophy. Sci Rep. 2017 09 19; 7(1):11877.
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Intermittent glucocorticoid steroid dosing enhances muscle repair without eliciting muscle atrophy. J Clin Invest. 2017 Jun 01; 127(6):2418-2432.