An expanding view for the molecular basis of familial periodic paralysis.
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Temperature dependence of erythromelalgia mutation L858F in sodium channel Nav1.7Channelopathies of skeletal muscle excitabilityNormokalemic periodic paralysis is not a distinct diseaseThe Genotype and Clinical Phenotype of Korean Patients with Familial Hypokalemic Periodic ParalysisHybrid assemblies of ATP-sensitive K+ channels determine their muscle-type-dependent biophysical and pharmacological propertiesSize matters: Erythromelalgia mutation S241T in Nav1.7 alters channel gating.Myasthenic syndrome caused by mutation of the SCN4A sodium channelHypokalemic periodic paralysis; two different genes responsible for similar clinical manifestations.Molecular biology of channelopathies: impact on diagnosis and treatment.The primary periodic paralyses: diagnosis, pathogenesis and treatment.Resting potential-dependent regulation of the voltage sensitivity of sodium channel gating in rat skeletal muscle in vivo.Equine metabolic myopathies with emphasis on the diagnostic approach. Comparison with human myopathies. A review.The dominant cold-sensitive Out-cold mutants of Drosophila melanogaster have novel missense mutations in the voltage-gated sodium channel gene paralyticHypokalemic Periodic Paralysis: a case report and review of the literatureInactivation of sodium channels underlies reversible neuropathy during critical illness in rats.Persistent human cardiac Na+ currents in stably transfected mammalian cells: Robust expression and distinct open-channel selectivity among Class 1 antiarrhythmics.Novel etiopathophysiological aspects of thyrotoxic periodic paralysis.Mexiletine block of wild-type and inactivation-deficient human skeletal muscle hNav1.4 Na+ channels.The Domain II S4-S5 Linker in Nav1.9: A Missense Mutation Enhances Activation, Impairs Fast Inactivation, and Produces Human Painful Neuropathy.An unusual pathologic feature and phenotype associated with familial hyperkalemic periodic paralysis.Design of a specific activator for skeletal muscle sodium channels uncovers channel architecture.[Thyrotoxic hypokalemic periodic paralysis, an endocrine emergency: clinical and genetic features in 25 patients].
P2860
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P2860
An expanding view for the molecular basis of familial periodic paralysis.
description
2002 nî lūn-bûn
@nan
2002 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2002年の論文
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2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
An expanding view for the molecular basis of familial periodic paralysis.
@ast
An expanding view for the molecular basis of familial periodic paralysis.
@en
An expanding view for the molecular basis of familial periodic paralysis.
@nl
type
label
An expanding view for the molecular basis of familial periodic paralysis.
@ast
An expanding view for the molecular basis of familial periodic paralysis.
@en
An expanding view for the molecular basis of familial periodic paralysis.
@nl
prefLabel
An expanding view for the molecular basis of familial periodic paralysis.
@ast
An expanding view for the molecular basis of familial periodic paralysis.
@en
An expanding view for the molecular basis of familial periodic paralysis.
@nl
P1476
An expanding view for the molecular basis of familial periodic paralysis.
@en
P2093
Stephen C Cannon
P304
P356
10.1016/S0960-8966(02)00007-X
P577
2002-08-01T00:00:00Z