"Channelopathies" 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.
A variety of neuromuscular conditions resulting from MUTATIONS in ION CHANNELS manifesting as episodes of EPILEPSY; HEADACHE DISORDERS; and DYSKINESIAS.
Descriptor ID |
D053447
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MeSH Number(s) |
C23.550.177
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Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Channelopathies".
Below are MeSH descriptors whose meaning is more specific than "Channelopathies".
This graph shows the total number of publications written about "Channelopathies" by people in this website by year, and whether "Channelopathies" 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 |
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2017 | 2 | 1 | 3 |
2018 | 3 | 0 | 3 |
2019 | 1 | 0 | 1 |
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Below are the most recent publications written about "Channelopathies" by people in Profiles.
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COVID-19 Infection and Corrected QT Interval Prolongation-Collateral Damage From Our Newest Enemy. JAMA Netw Open. 2021 04 01; 4(4):e217192.
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COVID-19 pandemia and inherited cardiomyopathies and channelopathies: a short term and long term perspective. Orphanet J Rare Dis. 2020 06 22; 15(1):157.
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Effects of curcumin on ion channels and pumps: A review. IUBMB Life. 2019 07; 71(7):812-820.
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Multiple sclerosis and non-dystrophic myotonias: do they share a common pathophysiology? Funct Neurol. 2018 Oct/Dec; 33(4):194-199.
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CRISPRed Cardiomyocytes to Decrypt Variants of Uncertain Significance. J Am Coll Cardiol. 2018 07 03; 72(1):76-78.
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Primary electrical disorders and arrhythmogenic right ventricular cardiomyopathy: new research insights with clinical implications. Europace. 2018 06 01; 20(FI1):f1-f2.
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The Italian subcutaneous implantable cardioverter-defibrillator survey: S-ICD, why not? Europace. 2017 Nov 01; 19(11):1826-1832.
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Genetic Testing in the Evaluation of Unexplained Cardiac Arrest: From the CASPER (Cardiac Arrest Survivors With Preserved Ejection Fraction Registry). Circ Cardiovasc Genet. 2017 Jun; 10(3).
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'Gardos Channelopathy': a variant of hereditary Stomatocytosis with complex molecular regulation. Sci Rep. 2017 05 11; 7(1):1744.