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Year Number of Results
1873 1
1993 1
1997 1
1999 2
2000 2
2001 6
2002 5
2003 2
2004 10
2005 6
2006 4
2007 8
2008 6
2009 4
2010 5
2011 5
2012 8
2013 8
2014 14
2015 7
2016 1
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2018 5
2019 9
2020 8
2021 14
2022 18
2023 10
2024 1

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Similar articles for PMID: 31380823

162 results

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Page 1
Hypokalemic periodic paralysis due to CACNA1S gene mutation.
Alhasan KA, Abdallah MS, Kari JA, Bashiri FA. Alhasan KA, et al. Neurosciences (Riyadh). 2019 Jul;24(3):225-230. doi: 10.17712/nsj.2018.3.20180005. Neurosciences (Riyadh). 2019. PMID: 31380823 Free PMC article.
The expanding phenotype of hypokalemic periodic paralysis in a Japanese family with p.Val876Glu mutation in CACNA1S.
Kurokawa M, Torio M, Ohkubo K, Tocan V, Ohyama N, Toda N, Ishii K, Nishiyama K, Mushimoto Y, Sakamoto R, Nakaza M, Horie R, Kubota T, Takahashi MP, Sakai Y, Nomura M, Ohga S. Kurokawa M, et al. Mol Genet Genomic Med. 2020 Apr;8(4):e1175. doi: 10.1002/mgg3.1175. Epub 2020 Feb 27. Mol Genet Genomic Med. 2020. PMID: 32104981 Free PMC article.
Hypokalemic Periodic Paralysis.
Weber F, Lehmann-Horn F. Weber F, et al. 2002 Apr 30 [updated 2018 Jul 26]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2002 Apr 30 [updated 2018 Jul 26]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301512 Free Books & Documents. Review.
162 results