Hypokalemic periodic paralysis

Known as: Primary Hypokalemic Periodic Paralysis, hypokalemic paralysis periodic, Familial Hypokalemic Periodic Paralysis 
An autosomal dominant familial disorder characterized by recurrent episodes of skeletal muscle weakness associated with falls in serum potassium… (More)

Topic mentions per year

Topic mentions per year

1941-2018
02040608019412017

Papers overview

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Highly Cited
2010
Highly Cited
2010
Thyrotoxic hypokalemic periodic paralysis (TPP) is characterized by acute attacks of weakness, hypokalemia, and thyrotoxicosis of… (More)
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Highly Cited
2007
Highly Cited
2007
The heritable muscle disorder hypokalemic periodic paralysis (HypoPP) is characterized by attacks of flaccid weakness, brought on… (More)
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2006
2006
Thyrotoxic periodic paralysis (TPP), familial periodic paralysis (FPP), and sporadic periodic paralysis (SPP) are the most common… (More)
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Highly Cited
2000
Highly Cited
2000
The pathomechanism of familial hypokalemic periodic paralysis (HypoPP) is a mystery, despite knowledge of the underlying dominant… (More)
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2000
2000
Missense mutations of the human skeletal muscle voltage-gated Na channel (hSkM1) underlie a variety of diseases, including… (More)
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1999
1999
OBJECTIVE To define how insulin acts in hypokalemic periodic paralysis (HypoPP). BACKGROUND HypoPP results from point mutations… (More)
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Highly Cited
1994
Highly Cited
1994
Hypokalemic periodic paralysis (hypoKPP) is an autosomal dominant skeletal muscle disorder manifested by episodic weakness… (More)
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Highly Cited
1994
Highly Cited
1994
The only calcium channel mutation reported to date is a deletion in the gene for the DHP-receptor alpha 1-subunit resulting in… (More)
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1986
1986
Generalized motor weakness is a common complaint in the emergency department and has a wide differential diagnosis that includes… (More)
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1984
1984
To study the mechanism of attacks in familial hypokalemic paralysis, we recorded resting membrane potentials, action potentials… (More)
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