histamine has been researched along with Hypokalemic Periodic Paralysis in 1 studies
Hypokalemic Periodic Paralysis: An autosomal dominant familial disorder characterized by recurrent episodes of skeletal muscle weakness associated with falls in serum potassium levels. The condition usually presents in the first or second decade of life with attacks of trunk and leg paresis during sleep or shortly after awakening. Symptoms may persist for hours to days and generally are precipitated by exercise or a meal high in carbohydrates. (Adams et al., Principles of Neurology, 6th ed, p1483)
| 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 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 |