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Normokalemic Periodic Paralysis

Known as: Periodic Paralyses, Normokalemic, Periodic Paralysis, Normokalemic, Paralysis, Normokalemic Periodic 
An autosomal dominant inherited non-dystrophic myotonia caused by mutations of the SCN4A gene, resulting in sodium muscle channelopathy. Currently… 
National Institutes of Health

Papers overview

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Highly Cited
2010
Highly Cited
2010
Hypokalemic periodic paralysis and normokalemic periodic paralysis are caused by mutations of the gating charge–carrying arginine… 
2009
2009
Hypokalemic tubular disorders may lead to growth retardation which is resistant to growth hormone (GH) treatment. The mechanism… 
Highly Cited
2008
Highly Cited
2008
Some inherited periodic paralyses are caused by mutations in skeletal muscle NaV1.4 sodium channels that alter channel gating and… 
2008
2008
ObjectiveIn this study, we aim to investigate the clinical features and Mutations of sodium channel α-subunit (SCN4A) genes in… 
Review
2006
Review
2006
The familial periodic paralyses (PP) were commonly considered to be benign diseases since frequency and severity of the paralytic… 
Highly Cited
2004
Highly Cited
2004
Background: Periodic paralysis is classified into hypokalemic (hypoPP) and hyperkalemic (hyperPP) periodic paralysis according to… 
2004
2004
BACKGROUND Angiotensin-converting enzyme (ACE) inhibitors and angiotensin II receptor blockers (ARBs) have shown numerous… 
2000
2000
Efforts to extend myocardial preservation for transplantation by crystalloid perfusion have been limited by edema and compromised… 
1994
1994
Many nutritional elements are known to have a key function in the normal growth and development of children. One such element… 
1983
1983
In 1963, Klein et al. first described two girls with normokalemic periodic paralysis and cardiac arrhythmia. We have observed a…