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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… Expand
National Institutes of Health

Papers overview

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Review
2018
Review
2018
Periodic paralyses (PPs) are rare neuromuscular disorders caused by mutations in skeletal muscle sodium, calcium, and potassium… Expand
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Highly Cited
2004
Highly Cited
2004
BACKGROUND Recurrent laryngeal nerve monitoring (RLNM) has been suspected to reduce postoperative RLN paralysis (RLNP). However… Expand
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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… Expand
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Highly Cited
1997
Highly Cited
1997
The concept of a conversion disorder (such as hysterical paralysis) has always been controversial (Ron, M.A. (1996). Somatization… Expand
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Highly Cited
1991
Highly Cited
1991
DNA from seven unrelated patients with hyperkalemic periodic paralysis (HYPP) was examined for mutations in the adult skeletal… Expand
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Highly Cited
1991
Highly Cited
1991
HYPERKALAEMIC periodic paralysis (HYPP)1 is an autosomal dominant disease that results in episodic electrical inexcitability and… Expand
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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… Expand
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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… Expand
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Highly Cited
1976
Highly Cited
1976
A syndrome of alveolar hypoventilation has been identified in a group of patients with bilateral diaphragm paralysis. Eight… Expand
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Highly Cited
1967
Highly Cited
1967
IN 1886 Eulenberg 1 described "paramyotonia congenita," an inherited syndrome in which episodes of myotonia and weakness were… Expand
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