histamine has been researched along with Familial Hypokalemic Periodic Paralysis in 1 studies
Excerpt | Relevance | Reference |
---|---|---|
"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." | 1.32 | A 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) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Kawamura, S | 1 |
Ikeda, Y | 1 |
Tomita, K | 1 |
Watanabe, N | 1 |
Seki, K | 1 |
1 other study available for histamine and Familial Hypokalemic Periodic Paralysis
Article | Year |
---|---|
A family of hypokalemic periodic paralysis with CACNA1S gene mutation showing incomplete penetrance in women.
Topics: Arginine; Calcium Channels; Calcium Channels, R-Type; Cation Transport Proteins; Exercise; Histamine | 2004 |