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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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2017
2017
Objectives. Normothermic hyperkalemic cardioplegia arrest (NHCA) may not effectively preserve hypertrophied myocardium during… 
2013
2013
Thyrotoxic Periodic Paralysis (TPP) is a rare and life threatening condition commonly occurring in young Asian males. It is… 
2012
2012
Introduction: Recent molecular studies of the original cases of normokalemic periodic paralysis (normoKPP) have raised suspicions… 
2008
2008
ObjectiveIn this study, we aim to investigate the clinical features and Mutations of sodium channel α-subunit (SCN4A) genes in… 
2008
2008
OBJECTIVE To construct and investigate the cell model of a novel mutation R675Q in the skeletal muscle Na channel type 4 alpha… 
Review
2004
Review
2004
OBJECTIVE In this report are reviewed two unrelated patients with typical normokalemic periodic paralysis (normoKPP) features and… 
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… 
1979
1979
A young man with episodes characteristic of familial normokalemic periodic paralysis was restudied after a change in the nature…