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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

97 related articles for article (PubMed ID: 15583983)

  • 1. [The mutation V781I in SCN4A gene exists in Chinese patients with normokalemic periodic paralysis].
    Guo XH; Wu WP; Zhang YH; Jia JP; Zhu K
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Dec; 21(6):566-9. PubMed ID: 15583983
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Screening SCN4A gene for mutations with denaturing high performance liquid chromatography technology in a Chinese family with normokalemic periodic paralysis].
    Guo XH; Wu WP; Zhang YH; Wang HB; Mao YL; Zhu K
    Zhonghua Yi Xue Za Zhi; 2004 Jan; 84(2):125-9. PubMed ID: 14990128
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Normokalemic periodic paralysis revisited: does it exist?
    Chinnery PF; Walls TJ; Hanna MG; Bates D; Fawcett PR
    Ann Neurol; 2002 Aug; 52(2):251-2. PubMed ID: 12210802
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Exercise test on the patients with normokalaemic periodic paralysis from a Chinese family with a mutation in the SCN4A gene.
    Feng Y; Zhang Y; Liu ZL; Zhang CD
    Chin Med J (Engl); 2008 Oct; 121(19):1915-9. PubMed ID: 19080124
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Normokalemic periodic paralysis is not a distinct disease.
    Song YW; Kim SJ; Heo TH; Kim MH; Kim JB
    Muscle Nerve; 2012 Dec; 46(6):914-6. PubMed ID: 22926674
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutations of sodium channel alpha-subunit genes in Chinese patients with normokalemic periodic paralysis.
    Xiuhai G; Weiping W; Ke Z; Hongbin W; Yiling S; MaoYanling
    Cell Mol Neurobiol; 2008 Aug; 28(5):653-61. PubMed ID: 18046642
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [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]  

  • 8. Novel mutations in families with unusual and variable disorders of the skeletal muscle sodium channel.
    McClatchey AI; McKenna-Yasek D; Cros D; Worthen HG; Kuncl RW; DeSilva SM; Cornblath DR; Gusella JF; Brown RH
    Nat Genet; 1992 Oct; 2(2):148-52. PubMed ID: 1338909
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Novel human pathological mutations. Gene symbol: SCN4A. Disease: Periodic paralysis.
    Hong D; Luan X; Chen B; Zheng R; Wang Z; Yuan Y
    Hum Genet; 2010 Jan; 127(1):113. PubMed ID: 20108424
    [No Abstract]   [Full Text] [Related]  

  • 10. Linkage of malignant hyperthermia and hyperkalemic periodic paralysis to the adult skeletal muscle sodium channel (SCN4A) gene in a large pedigree.
    Moslehi R; Langlois S; Yam I; Friedman JM
    Am J Med Genet; 1998 Feb; 76(1):21-7. PubMed ID: 9508059
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Successful treatment of normokalemic periodic paralysis with hydrochlorothiazide.
    Akaba Y; Takahashi S; Sasaki Y; Kajino H
    Brain Dev; 2018 Oct; 40(9):833-836. PubMed ID: 29907477
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identification of a
    Tan X; Hu S; Xie Z; Mei H; Liu Y; Yin L; Shi P; Chen Q; Sang D
    J Int Med Res; 2020 Sep; 48(9):300060520953643. PubMed ID: 32962503
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. [The construction and preliminary investigation of the cell model of a novel mutation R675Q in the SCN4A gene identified in a Chinese family with normokalemic periodic paralysis].
    Wu L; Wu W; Yan G; Wang X; Liu J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Dec; 25(6):629-32. PubMed ID: 19065518
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Detection of alpha-galactosidase a mutations causing Fabry disease by denaturing high performance liquid chromatography.
    Shabbeer J; Robinson M; Desnick RJ
    Hum Mutat; 2005 Mar; 25(3):299-305. PubMed ID: 15712228
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mutational analysis of the NF2 gene in sporadic meningiomas by denaturing high-performance liquid chromatography.
    Kim JH; Kim IS; Kwon SY; Jang BC; Suh SI; Shin DH; Jeon CH; Son EI; Kim SP
    Int J Mol Med; 2006 Jul; 18(1):27-32. PubMed ID: 16786152
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [R1239H mutation of CACNA1S gene in a Chinese family with hypokalaemic periodic paralysis].
    Ke Q; Wu WP; Guo XH; Xu QG; Huang DH; Mao YL; Huo CN
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Jun; 23(3):272-4. PubMed ID: 16767662
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Familial periodic paralysis and Charcot-Marie-Tooth disease in a 7-generation family.
    Hisama FM
    Arch Neurol; 2005 Jan; 62(1):135-8. PubMed ID: 15642860
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mutation screening in Korean hypokalemic periodic paralysis patients: a novel SCN4A Arg672Cys mutation.
    Kim MK; Lee SH; Park MS; Kim BC; Cho KH; Lee MC; Kim JH; Kim SM
    Neuromuscul Disord; 2004 Nov; 14(11):727-31. PubMed ID: 15482957
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Periodic paralysis in quarter horses: a sodium channel mutation disseminated by selective breeding.
    Rudolph JA; Spier SJ; Byrns G; Rojas CV; Bernoco D; Hoffman EP
    Nat Genet; 1992 Oct; 2(2):144-7. PubMed ID: 1338908
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.