Normokalemic periodic paralysis is not a distinct disease
Author:
Publisher
Wiley
Subject
Physiology (medical),Cellular and Molecular Neuroscience,Neurology (clinical),Physiology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/mus.23441/fullpdf
Reference12 articles.
1. Normokalemic periodic paralysis revisited: does it exist?;Chinnery;Ann Neurol,2002
2. New mutations of SCN4A cause a potassium-sensitive normokalemic periodic paralysis;Vicart;Neurology,2004
3. From mutation to myotonia in sodium channel disorders;Cannon;Neuromuscul Disord,1997
4. Identification of a mutation in the gene causing hyperkalemic periodic paralysis;Ptacek;Cell,1993
5. A Met-to-Val mutation in the skeletal muscle Na+ channel alpha-subunit in hyperkalaemic periodic paralysis;Rojas;Nature,1991
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1. Genetic analysis of 37 cases with primary periodic paralysis in Chinese patients;Orphanet Journal of Rare Diseases;2024-04-12
2. Prevalence and risk factors of low vitamin D levels in children and adolescents with familial hypokalemic periodic paralysis;European Journal of Pediatrics;2023-10-25
3. The clinical and genetic heterogeneity analysis of five families with primary periodic paralysis;Channels;2020-12-21
4. SCN4A p.R675Q Mutation Leading to Normokalemic Periodic Paralysis: A Family Report and Literature Review;Frontiers in Neurology;2019-10-25
5. Familial Normokalemic Periodic Paralysis Associated With Mutation in the SCN4A p.M1592V;Frontiers in Neurology;2018-06-07
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