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histamine and Familial Hypokalemic Periodic Paralysis

histamine has been researched along with Familial Hypokalemic Periodic Paralysis in 1 studies

Research Excerpts

ExcerptRelevanceReference
"Familial hypokalemic periodic paralysis is an autosomal dominant genetic muscle disease characterized by periodic attacks of muscle weakness associated with a decrease in serum potassium."1.32A family of hypokalemic periodic paralysis with CACNA1S gene mutation showing incomplete penetrance in women. ( Ikeda, Y; Kawamura, S; Seki, K; Tomita, K; Watanabe, N, 2004)

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Kawamura, S1
Ikeda, Y1
Tomita, K1
Watanabe, N1
Seki, K1

Other Studies

1 other study available for histamine and Familial Hypokalemic Periodic Paralysis

ArticleYear
A family of hypokalemic periodic paralysis with CACNA1S gene mutation showing incomplete penetrance in women.
    Internal medicine (Tokyo, Japan), 2004, Volume: 43, Issue:3

    Topics: Arginine; Calcium Channels; Calcium Channels, R-Type; Cation Transport Proteins; Exercise; Histamine

2004