Paralyses, Familial Periodic
"Paralyses, Familial Periodic" 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 heterogenous group of inherited disorders characterized by recurring attacks of rapidly progressive flaccid paralysis or myotonia. These conditions have in common a mutation of the gene encoding the alpha subunit of the sodium channel in skeletal muscle. They are frequently associated with fluctuations in serum potassium levels. Periodic paralysis may also occur as a non-familial process secondary to THYROTOXICOSIS and other conditions. (From Adams et al., Principles of Neurology, 6th ed, p1481)
MeSH Number(s)
C05.651.701
C10.668.491.650
C16.320.565.618.711
C18.452.648.618.711
Concept/Terms
Paralyses, Familial Periodic- Paralyses, Familial Periodic
- Familial Periodic Paralyses
- Periodic Paralyses, Familial
- Familial Periodic Paralysis
- Periodic Paralysis, Familial
- Paralysis, Familial Periodic
Normokalemic Periodic Paralysis- Normokalemic Periodic Paralysis
- Normokalemic Periodic Paralyses
- Paralyses, Normokalemic Periodic
- Paralysis, Normokalemic Periodic
- Periodic Paralyses, Normokalemic
- Periodic Paralysis, Normokalemic
Below are MeSH descriptors whose meaning is more general than "Paralyses, Familial Periodic".
- Diseases [C]
- Musculoskeletal Diseases [C05]
- Muscular Diseases [C05.651]
- Paralyses, Familial Periodic [C05.651.701]
- Nervous System Diseases [C10]
- Neuromuscular Diseases [C10.668]
- Muscular Diseases [C10.668.491]
- Paralyses, Familial Periodic [C10.668.491.650]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
- Metabolism, Inborn Errors [C16.320.565]
- Metal Metabolism, Inborn Errors [C16.320.565.618]
- Paralyses, Familial Periodic [C16.320.565.618.711]
- Nutritional and Metabolic Diseases [C18]
- Metabolic Diseases [C18.452]
- Metabolism, Inborn Errors [C18.452.648]
- Metal Metabolism, Inborn Errors [C18.452.648.618]
- Paralyses, Familial Periodic [C18.452.648.618.711]
Below are MeSH descriptors whose meaning is more specific than "Paralyses, Familial Periodic".
This graph shows the total number of publications written about "Paralyses, Familial Periodic" by people in Harvard Catalyst Profiles by year, and whether "Paralyses, Familial Periodic" was a major or minor topic of these publication.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1993 | 2 | 0 | 2 |
| 1998 | 1 | 0 | 1 |
| 2002 | 1 | 0 | 1 |
| 2014 | 1 | 0 | 1 |
| 2019 | 1 | 0 | 1 |
Below are the most recent publications written about "Paralyses, Familial Periodic" by people in Profiles.
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Acute Neuromuscular Disorders in the Pediatric Intensive Care Unit. J Child Neurol. 2020 01; 35(1):17-24.
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Novel mutations in human and mouse SCN4A implicate AMPK in myotonia and periodic paralysis. Brain. 2014 Dec; 137(Pt 12):3171-85.
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[A case of normokalemic periodic paralysis]. Zhongguo Zhen Jiu. 2013 May; 33(5):425.
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A rare case of thyrotoxic periodic paralysis with normokalemia. J Endocrinol Invest. 2013 Feb; 36(2):146.
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Phosphorylation and protonation of neighboring MiRP2 sites: function and pathophysiology of MiRP2-Kv3.4 potassium channels in periodic paralysis. FASEB J. 2006 Feb; 20(2):293-301.
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Familial periodic paralysis and Charcot-Marie-Tooth disease in a 7-generation family. Arch Neurol. 2005 Jan; 62(1):135-8.
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A glutamate residue at the C terminus regulates activity of inward rectifier K+ channels: implication for Andersen's syndrome. Proc Natl Acad Sci U S A. 2002 Jun 11; 99(12):8430-5.
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MiRP2 forms potassium channels in skeletal muscle with Kv3.4 and is associated with periodic paralysis. Cell. 2001 Jan 26; 104(2):217-31.
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Thyrotoxic periodic paralysis in a Jamaican male. J Emerg Med. 1999 Jan-Feb; 17(1):47-51.
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Gating of the L-type Ca channel in human skeletal myotubes: an activation defect caused by the hypokalemic periodic paralysis mutation R528H. J Neurosci. 1998 Dec 15; 18(24):10320-34.