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 *

319 related articles for article (PubMed ID: 25088161)

  • 1. Cardiac arrhythmias in hypokalemic periodic paralysis: Hypokalemia as only cause?
    Stunnenberg BC; Deinum J; Links TP; Wilde AA; Franssen H; Drost G
    Muscle Nerve; 2014 Sep; 50(3):327-32. PubMed ID: 25088161
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mutations associated with hypokalemic periodic paralysis: from hotspot regions to complete analysis of CACNA1S and SCN4A genes.
    Brugnoni R; Canioni E; Filosto M; Pini A; Tonin P; Rossi T; Canavese C; Eoli M; Siciliano G; Lauria G; Mantegazza R; Maggi L
    Neurogenetics; 2022 Jan; 23(1):19-25. PubMed ID: 34608571
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Sinus arrest in familial hypokalemic periodic paralysis caused by SCN4A mutation: a case report.
    Bui TD; Pham ND; Phan-Nguyen TV; Vu-Thi LN; Tran VT; Nguyen VH; Nguyen MD; Tran H
    Eur Rev Med Pharmacol Sci; 2023 Mar; 27(5):1767-1773. PubMed ID: 36930492
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Severe prognosis in a large family with hypokalemic periodic paralysis.
    Caciotti A; Morrone A; Domenici R; Donati MA; Zammarchi E
    Muscle Nerve; 2003 Feb; 27(2):165-9. PubMed ID: 12548523
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Gender differences in penetrance and phenotype in hypokalemic periodic paralysis.
    Ke Q; Luo B; Qi M; Du Y; Wu W
    Muscle Nerve; 2013 Jan; 47(1):41-5. PubMed ID: 23019082
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Sodium channel gene mutations in hypokalemic periodic paralysis: an uncommon cause in the UK.
    Davies NP; Eunson LH; Samuel M; Hanna MG
    Neurology; 2001 Oct; 57(7):1323-5. PubMed ID: 11591859
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Progressive muscle atrophy with hypokalemic periodic paralysis and calcium channel mutation.
    Meyer T; Jurkat-Rott K; Huebner A; Lehmann-Horn F; Linke P; Van Landeghem F; Dullinger JS; Spuler S
    Muscle Nerve; 2008 Jan; 37(1):120-4. PubMed ID: 17587224
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4A.
    Sternberg D; Maisonobe T; Jurkat-Rott K; Nicole S; Launay E; Chauveau D; Tabti N; Lehmann-Horn F; Hainque B; Fontaine B
    Brain; 2001 Jun; 124(Pt 6):1091-9. PubMed ID: 11353725
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a South American family.
    Ke T; Gomez CR; Mateus HE; Castano JA; Wang QK
    J Hum Genet; 2009 Nov; 54(11):660-4. PubMed ID: 19779499
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Voltage-dependent Ca
    DiFranco M; Cannon SC
    Am J Physiol Cell Physiol; 2022 Aug; 323(2):C478-C485. PubMed ID: 35759432
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Hypokalemic periodic paralysis due to the SCN4A R672H mutation in a Turkish family.
    Incecik F; Hergüner MO; Altunbaşak S; Lehman-Horn F
    Turk J Pediatr; 2010; 52(4):409-10. PubMed ID: 21043388
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The genotype and clinical phenotype of Korean patients with familial hypokalemic periodic paralysis.
    Kim JB; Kim MH; Lee SJ; Kim DJ; Lee BC
    J Korean Med Sci; 2007 Dec; 22(6):946-51. PubMed ID: 18162704
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mutation analysis of CACNA1S and SCN4A in patients with hypokalemic periodic paralysis.
    Wang XY; Ren BW; Yong ZH; Xu HY; Fu QX; Yao HB
    Mol Med Rep; 2015 Oct; 12(4):6267-74. PubMed ID: 26252573
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The clinical and genetic heterogeneity analysis of five families with primary periodic paralysis.
    Wang Q; Zhao Z; Shen H; Bing Q; Li N; Hu J
    Channels (Austin); 2021 Dec; 15(1):20-30. PubMed ID: 33345742
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A novel CACNA1S gene variant in a child with hypokalemic periodic paralysis: a case report and literature review.
    Zhou W; Zhao P; Gao J; Zhang Y
    BMC Pediatr; 2023 Oct; 23(1):500. PubMed ID: 37784084
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genotype and phenotype analysis of patients with sporadic periodic paralysis.
    Sung CC; Cheng CJ; Lo YF; Lin MS; Yang SS; Hsu YC; Lin SH
    Am J Med Sci; 2012 Apr; 343(4):281-5. PubMed ID: 21841462
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel mutation in the calcium channel gene in a family with hypokalemic periodic paralysis.
    Hirano M; Kokunai Y; Nagai A; Nakamura Y; Saigoh K; Kusunoki S; Takahashi MP
    J Neurol Sci; 2011 Oct; 309(1-2):9-11. PubMed ID: 21855088
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Muscle edema of the lower limb determined by MRI in Asian hypokalaemic periodic paralysis patients.
    Jia BX; Yang Q; Li SY; Wan M; Wang H; Huo LY; Zhao E; Ding YC; Ji XM; Guo XH
    Neurol Res; 2015 Mar; 37(3):246-52. PubMed ID: 25213595
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Gene analysis of the calcium channel 1 subunit and clinical studies for two patients with hypokalemic periodic paralysis.
    Kageyama K; Terui K; Tsutaya S; Matsuda E; Shoji M; Sakihara S; Nigawara T; Takayasu S; Moriyama T; Yasujima M; Suda T
    J Endocrinol Invest; 2006 Nov; 29(10):928-33. PubMed ID: 17185904
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic analysis of 37 cases with primary periodic paralysis in Chinese patients.
    Zhao X; Ning H; Liu L; Zhu C; Zhang Y; Sun G; Ren H; Kong X
    Orphanet J Rare Dis; 2024 Apr; 19(1):160. PubMed ID: 38609989
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.