An atypical phenotype of hypokalemic periodic paralysis caused by a mutation in the sodium channel gene SCN4A
Yang Hee Park (Park YH), June Bum Kim (Kim JB)
Clin Exp Pediatr. 2010;53(10):909-912.   Published online 2010 Oct 31     DOI: https://doi.org/10.3345/kjp.2010.53.10.909
Citations to this article as recorded by Crossref logo
Ramen noodle neuropathy: an atypical case of partial paralysis from malnutrition
Adam Lalley, Sabrina Bawa, Elie Harmouche
The American Journal of Emergency Medicine.2024; 75: 198.e7.     CrossRef
Novel compound heterozygous mutations in SCN4A as a potential genetic cause contributing to myopathic manifestations: A case report and literature review
Ji Yoon Han, Joonhong Park
Heliyon.2024; 10(7): e28684.     CrossRef
Prevalence and risk factors of low vitamin D levels in children and adolescents with familial hypokalemic periodic paralysis
Jae-Hoon Min, Ji Young Lee, Hye-Sung Ahn, Hui Song Cui, Cheong Hoon Seo, June-Bum Kim
European Journal of Pediatrics.2023; 183(1): 305.     CrossRef
NaV1.4 DI-S4 periodic paralysis mutation R222W enhances inactivation and promotes leak current to attenuate action potentials and depolarize muscle fibers
Landon Bayless-Edwards, Vern Winston, Frank Lehmann-Horn, Paula Arinze, James R. Groome, Karin Jurkat-Rott
Scientific Reports.2018;[Epub]     CrossRef
N1366S mutation of human skeletal muscle sodium channel causes paramyotonia congenita
Qing Ke, Jia Ye, Siyang Tang, Jin Wang, Benyan Luo, Fang Ji, Xu Zhang, Ye Yu, Xiaoyang Cheng, Yuezhou Li
The Journal of Physiology.2017; 595(22): 6837.     CrossRef
SPORADİK HİPOPOTASEMİK PERİYODİK PARALİZİ: OLGU SUNUMU
Aslı Ece ÇİLLİLER
Kocatepe Tıp Dergisi.2017; : 67.     CrossRef
Gating pore currents are defects in common with two Nav1.5 mutations in patients with mixed arrhythmias and dilated cardiomyopathy
Adrien Moreau, Pascal Gosselin-Badaroudine, Lucie Delemotte, Michael L. Klein, Mohamed Chahine
Journal of General Physiology.2015; 145(2): 93.     CrossRef
Mutation analysis of CACNA1S and SCN4A in patients with hypokalemic periodic paralysis
XIAO-YING WANG, BING-WEN REN, ZENG-HUA YONG, HONG-YAN XU, QIU-XIA FU, HE-BIN YAO
Molecular Medicine Reports.2015; 12(4): 6267.     CrossRef
The large-conductance calcium-activated potassium channel holds the key to the conundrum of familial hypokalemic periodic paralysis
June-Bum Kim, Sung-Jo Kim, Sun-Yang Kang, Jin Woong Yi, Seung-Min Kim
Korean Journal of Pediatrics.2014; 57(10): 445.     CrossRef
Cloning and expression of the two new variants of Nav1.5/SCN5A in rat brain
Cheng-Tao Ren, Dong-Mei Li, Shao-Wu Ou, Yun-Jie Wang, Yi Lin, Zhi-Hong Zong, Masaki Kameyama, Asako Kameyama
Molecular and Cellular Biochemistry.2012; 365(1-2): 139.     CrossRef
Normokalemic periodic paralysis is not a distinct disease
Young‐Wha Song, Sung‐Jo Kim, Tae‐Hwe Heo, Man‐Ho Kim, June‐Bum Kim
Muscle & Nerve.2012; 46(6): 908.     CrossRef
Familial hyperkalemic periodic paralysis caused by ade novomutation in the sodium channel geneSCN4A
Ji-Yeon Han, June-Bum Kim
Korean Journal of Pediatrics.2011; 54(11): 470.     CrossRef