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… (More)
National Institutes of Health

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Highly Cited
2001
Highly Cited
2001
The subthreshold, voltage-gated potassium channel of skeletal muscle is shown to contain MinK-related peptide 2 (MiRP2) and the… (More)
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Review
1997
Review
1997
Hyperkalemic periodic paralysis is an autosomal codominant genetic disease of horses who are descendants of the quarter horse… (More)
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1993
1993
Hyperkalemic periodic paralysis (HYPP), one of several inheritable myotonic diseases, results from genetic defects in the human… (More)
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1993
1993
Clinical and electrophysiological data have outlined a spectrum of similar yet distinct periodic paralyses, including potassium… (More)
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1991
1991
DNA from seven unrelated patients with hyperkalemic periodic paralysis (HYPP) was examined for mutations in the adult skeletal… (More)
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Highly Cited
1991
Highly Cited
1991
Hyperkalemic periodic analysis (HPP) is an autosomal dominant disorder characterized by episodic weakness lasting minutes to days… (More)
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1990
1990
A progressive degenerative myopathy has been well described in hypokalemic periodic paralysis but is not as widely recognized in… (More)
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Highly Cited
1990
Highly Cited
1990
Hyperkalemic periodic paralysis (HYPP) is an autosomal dominant disorder characterized by episodes of muscle weakness due to… (More)
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1990
1990
Eleven horses (3 mares, 7 stallions, 1 gelding) with clinical and biochemical evidence of hyperkalemic periodic paralysis were… (More)
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1967
1967
Hyperkalemic periodic paralysis is a condition that causes episodes of extreme muscle weakness or paralysis, usually beginning in… (More)
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