The Genotype and Clinical Phenotype of Korean Patients with Familial Hypokalemic Periodic Paralysis
about
Practical aspects in the management of hypokalemic periodic paralysisChannelopathiesTherapeutic Approaches to Genetic Ion Channelopathies and Perspectives in Drug DiscoveryNormokalemic periodic paralysis is not a distinct diseaseRecent 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 channelopathiesMuscle channelopathies: does the predicted channel gating pore offer new treatment insights for hypokalaemic periodic paralysis?Familial hyperkalemic periodic paralysis caused by a de novo mutation in the sodium channel gene SCN4A.The large-conductance calcium-activated potassium channel holds the key to the conundrum of familial hypokalemic periodic paralysis.
P2860
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P2860
The Genotype and Clinical Phenotype of Korean Patients with Familial Hypokalemic Periodic Paralysis
description
2007 nî lūn-bûn
@nan
2007 թուականին հրատարակուած գիտական յօդուած
@hyw
2007 թվականին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
The Genotype and Clinical Phen ...... Hypokalemic Periodic Paralysis
@ast
The Genotype and Clinical Phen ...... Hypokalemic Periodic Paralysis
@en
type
label
The Genotype and Clinical Phen ...... Hypokalemic Periodic Paralysis
@ast
The Genotype and Clinical Phen ...... Hypokalemic Periodic Paralysis
@en
prefLabel
The Genotype and Clinical Phen ...... Hypokalemic Periodic Paralysis
@ast
The Genotype and Clinical Phen ...... Hypokalemic Periodic Paralysis
@en
P2093
P2860
P3181
P1476
The Genotype and Clinical Phen ...... Hypokalemic Periodic Paralysis
@en
P2093
Byung Churl Lee
Dae-Joong Kim
June-Bum Kim
Man-Ho Kim
Soon Ju Lee
P2860
P3181
P356
10.3346/JKMS.2007.22.6.946
P577
2007-01-01T00:00:00Z