"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.
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Year | Major Topic | Minor Topic | Total |
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2007 | 1 | 0 | 1 |
2008 | 1 | 0 | 1 |
2009 | 0 | 1 | 1 |
2016 | 2 | 0 | 2 |
2017 | 1 | 0 | 1 |
2022 | 1 | 0 | 1 |
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Below are the most recent publications written about "Channelopathies" by people in Profiles.
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Complex effects on CaV2.1 channel gating caused by a CACNA1A variant associated with a severe neurodevelopmental disorder. Sci Rep. 2022 06 02; 12(1):9186.
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Precision physiology and rescue of brain ion channel disorders. J Gen Physiol. 2017 May 01; 149(5):533-546.
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Rare neurological channelopathies--networks to study patients, pathogenesis and treatment. Nat Rev Neurol. 2016 Apr; 12(4):195-203.
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PITX2: a master regulator of cardiac channelopathy in atrial fibrillation? Cardiovasc Res. 2016 Mar 01; 109(3):345-7.
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Kv4.2 knockout mice demonstrate increased susceptibility to convulsant stimulation. Epilepsia. 2009 Jul; 50(7):1741-51.
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T-type calcium channels: from discovery to channelopathies, 25 years of research. Channels (Austin). 2008 Jul-Aug; 2(4):299-302.
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[Genetics of epilepsy]. Medicina (B Aires). 2007; 67(6 Pt 1):601-13.