These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
187 related articles for article (PubMed ID: 24943082)
1. [Normokalemic periodic paralysis lasting for two weeks: a severe form of sodium channelopathy with M1592V mutation]. Shiga K; Mizuta I; Noto Y; Nakagawa M; Sasaki R; Yamawaki M Rinsho Shinkeigaku; 2014; 54(5):434-9. PubMed ID: 24943082 [TBL] [Abstract][Full Text] [Related]
2. "Status myotonicus" in Na Rempe T; Subramony SH Neuromuscul Disord; 2020 May; 30(5):424-426. PubMed ID: 32327288 [TBL] [Abstract][Full Text] [Related]
3. Clinical and genetic spectrum of a Chinese cohort with SCN4A gene mutations. Sun J; Luo S; Suetterlin KJ; Song J; Huang J; Zhu W; Xi J; Zhou L; Lu J; Lu J; Zhao C; Hanna MG; Männikkö R; Matthews E; Qiao K Neuromuscul Disord; 2021 Sep; 31(9):829-838. PubMed ID: 33965302 [TBL] [Abstract][Full Text] [Related]
4. [Clinical and molecular genetic analysis of a family with normokalemic periodic paralysis]. Wei CJ; Wang D; Wang S; Jiao H; Hong DJ; Pu LH; Xiong H Zhonghua Er Ke Za Zhi; 2013 Jan; 51(1):47-51. PubMed ID: 23527931 [TBL] [Abstract][Full Text] [Related]
5. Prevalence study of genetically defined skeletal muscle channelopathies in England. Horga A; Raja Rayan DL; Matthews E; Sud R; Fialho D; Durran SC; Burge JA; Portaro S; Davis MB; Haworth A; Hanna MG Neurology; 2013 Apr; 80(16):1472-5. PubMed ID: 23516313 [TBL] [Abstract][Full Text] [Related]
13. Mutation spectrum and health status in skeletal muscle channelopathies in Japan. Sasaki R; Nakaza M; Furuta M; Fujino H; Kubota T; Takahashi MP Neuromuscul Disord; 2020 Jul; 30(7):546-553. PubMed ID: 32660787 [TBL] [Abstract][Full Text] [Related]
14. [A case of muscle sodium channelopathy with markedly high value of serum creatine kinase and mild eyelid myotonia]. Kasama S; Kimura T; Kajiyama K; Takeda M; Takahashi MP; Yoshikawa H Rinsho Shinkeigaku; 2011 Feb; 51(2):120-4. PubMed ID: 21404612 [TBL] [Abstract][Full Text] [Related]
15. Paralysis periodica paramyotonica caused by SCN4A Arg1448Cys mutation. Hsu WC; Huang YC; Wang CW; Hsueh CH; Lai LP; Yeh JH J Formos Med Assoc; 2006 Jun; 105(6):503-7. PubMed ID: 16801039 [TBL] [Abstract][Full Text] [Related]
16. [Analysis of SCN4A gene variation in a Chinese pedigree affected with skeletal muscle sodium channelopathies]. Lu Y; Yang X; Wang X; Xue P; Zhang J; Li Y Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Aug; 36(8):809-812. PubMed ID: 31400134 [TBL] [Abstract][Full Text] [Related]
17. Normokalemic periodic paralysis with involuntary movements and generalized epilepsy associated with two novel mutations in SCN4A gene. Cao L; Li X; Hong D Seizure; 2015 Jan; 24():134-6. PubMed ID: 25193600 [No Abstract] [Full Text] [Related]
18. SCN4A variants and Brugada syndrome: phenotypic and genotypic overlap between cardiac and skeletal muscle sodium channelopathies. Bissay V; Van Malderen SC; Keymolen K; Lissens W; Peeters U; Daneels D; Jansen AC; Pappaert G; Brugada P; De Keyser J; Van Dooren S Eur J Hum Genet; 2016 Mar; 24(3):400-7. PubMed ID: 26036855 [TBL] [Abstract][Full Text] [Related]
19. Phenotypic variation of a Thr704Met mutation in skeletal sodium channel gene in a family with paralysis periodica paramyotonica. Kim J; Hahn Y; Sohn EH; Lee YJ; Yun JH; Kim JM; Chung JH J Neurol Neurosurg Psychiatry; 2001 May; 70(5):618-23. PubMed ID: 11309455 [TBL] [Abstract][Full Text] [Related]
20. Familial Normokalemic Periodic Paralysis Associated With Mutation in the Fu C; Wang Z; Wang L; Li J; Sang Q; Chen J; Qi L; Jin H; Liu X Front Neurol; 2018; 9():430. PubMed ID: 29930533 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]