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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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Review
2019
Review
2019
A woman in her mid-30’s with salt-losing 21-hydroxylase deficiency diagnosed in neonatal period had been supplemented glucoand… 
2014
2014
Hyperthyroidism presents with a myriad of symptoms and signs, periodic paralysis is rare among them. Thyrotoxic periodic… 
2013
2013
Thyrotoxic Periodic Paralysis (TPP) is a rare and life threatening condition commonly occurring in young Asian males. It is… 
2011
2011
Objective In this report are analysis two unrelated patients with typical normokalemic periodic paralysis(NormoKPP) features and… 
2006
2006
Familial periodic paralysis (PP) is an autosomal dominant disorder characterized by episodic attacks of paralysis with different… 
2004
2004
目的 报道正常血钾型周期性麻痹(normoPP)一家系的临床特点,并筛查SCN4A基因以期发现有义突变.方法提取知情同意的患者及部分家属外周血基因组DNA,应用变性高效液相色谱分析(DHPLC)技术筛查患者SCN4A基因全部24… 
2004
2004
Objective To detect a novel mutation in SCN4A gene related to normokalemic periodic paralysis (normoPP) in one Chinese family… 
2003
2003
Objective To discuss the clinical features of normokalemic periodic paralysis (normoPP) and try to clarify the associations… 
1983
1983
This study was undertaken to examine the effects of lidocaine (L) (400 mg/liter) in a normokalemic crystalloid (S) (K +: 5 meq… 
1978
1978
Sarcoplasmic reticulum (SR) vesicles were isolated from muscle biopsies of 4 normal volunteers, a patient with McArdle disease…