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Hyperkalemic periodic paralysis

Known as: Gamstorp Episodic Adynamy, Primary Hyperkalemic Periodic Paralysis, Myotonic Periodic Paralysis 
An autosomal dominant familial disorder which presents in infancy or childhood and is characterized by episodes of weakness associated with… 
National Institutes of Health

Papers overview

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Highly Cited
2002
Highly Cited
2002
The transition from surface to bulk pentacene at the Au(111) interface will have important implications for the mechanism of… 
1999
1999
A 24-year-old man with sporadic hyperkalemic periodic paralysis (HPP) presented with moderate excessive daytime sleepiness and… 
1991
1991
The attachment sites of female Karoo paralysis ticks (Ixodes rubicundus) and equations to assess tick burdens on domestic (sheep… 
1984
1984
Medullary sponge kidney associated with a defect in urine acidification is rare and usually of no clinical significance. We… 
1974
1974
Rates of potassium influx in red blood cells of three patients with hyperkalemic periodic paralysis were studied during attack… 
1962
1962
Excerpt In 1956 Gamstorp (1) of the University of Lund, Sweden, reported her observations of a hereditary disorder manifested by… 
Review
1934
Review
1934
The condition known as "family periodic paralysis," "paroxysmal paralysis" and "myoplegia periodica" was recognized as a clinical…