Sodium channel inactivation defects are associated with acetazolamide-exacerbated hypokalemic periodic paralysis.
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Treatment for periodic paralysisTherapeutic Approaches to Genetic Ion Channelopathies and Perspectives in Drug DiscoveryPhysiological and Pathophysiological Insights of Nav1.4 and Nav1.5 ComparisonThe Genotype and Clinical Phenotype of Korean Patients with Familial Hypokalemic Periodic ParalysisA Korean family of hypokalemic periodic paralysis with mutation in a voltage-gated calcium channel (R1239G)Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysisIon permeation and block of the gating pore in the voltage sensor of NaV1.4 channels with hypokalemic periodic paralysis mutationsAn atypical phenotype of hypokalemic periodic paralysis caused by a mutation in the sodium channel gene SCN4A.Primary periodic paralyses.Recent advances in the pathogenesis and drug action in periodic paralyses and related channelopathies.Hypokalemic periodic paralysis; two different genes responsible for similar clinical manifestations.Pathophysiological role of omega pore current in channelopathiesThe primary periodic paralyses: diagnosis, pathogenesis and treatment.Voltage-gated sodium channels: action players with many faces.Hypokalemic periodic paralysis: a model for a clinical and research approach to a rare disorder.Randomized, placebo-controlled trials of dichlorphenamide in periodic paralysis.Bumetanide prevents transient decreases in muscle force in murine hypokalemic periodic paralysis.Depolarization-activated gating pore current conducted by mutant sodium channels in potassium-sensitive normokalemic periodic paralysisMuscle channelopathies: does the predicted channel gating pore offer new treatment insights for hypokalaemic periodic paralysis?Skeletal muscle na channel disorders.Mechanisms underlying a life-threatening skeletal muscle Na+ channel disorder.Hypokalaemia and dysmorphia, is there a link?Review of the Diagnosis and Treatment of Periodic Paralysis.Antioxidants reverse depression of the hypoxic ventilatory response by acetazolamide in man.N1366S mutation of human skeletal muscle sodium channel causes paramyotonia congenita.Interaction between fast and ultra-slow inactivation in the voltage-gated sodium channel. Does the inactivation gate stabilize the channel structure?Hypokalemic periodic paralysis in a patient with acquired growth hormone deficiency.Thyrotoxic periodic paralysis associated with a mutation in the sodium channel gene SCN4A.Gating Pore Currents in Sodium Channels
P2860
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P2860
Sodium channel inactivation defects are associated with acetazolamide-exacerbated hypokalemic periodic paralysis.
description
2001 nî lūn-bûn
@nan
2001年の論文
@ja
2001年学术文章
@wuu
2001年学术文章
@zh-cn
2001年学术文章
@zh-hans
2001年学术文章
@zh-my
2001年学术文章
@zh-sg
2001年學術文章
@yue
2001年學術文章
@zh
2001年學術文章
@zh-hant
name
Sodium channel inactivation de ...... ypokalemic periodic paralysis.
@en
type
label
Sodium channel inactivation de ...... ypokalemic periodic paralysis.
@en
prefLabel
Sodium channel inactivation de ...... ypokalemic periodic paralysis.
@en
P2093
P2860
P356
P1433
P1476
Sodium channel inactivation de ...... ypokalemic periodic paralysis.
@en
P2093
P2860
P304
P356
10.1002/ANA.1144
P577
2001-09-01T00:00:00Z