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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1971 2
1975 5
1976 5
1977 1
1978 4
1979 8
1980 4
1981 1
1982 6
1983 4
1984 2
1985 2
1986 5
1987 4
1988 6
1989 3
1990 1
1991 16
1992 12
1993 15
1994 10
1995 10
1996 14
1997 10
1998 10
1999 13
2000 7
2001 4
2002 10
2003 8
2004 6
2005 5
2006 11
2007 11
2008 12
2009 4
2010 9
2011 14
2012 15
2013 26
2014 19
2015 16
2016 20
2017 23
2018 19
2019 22
2020 30
2021 26
2022 23
2023 18
2024 4

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PubMed for id: 10158

500 results

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Page 1
Clinical and Genetic Spectrum of Myotonia Congenita in Turkish Children.
Öz Tunçer G, Sanri A, Aydin S, Hergüner ÖM, Özgün N, Kömür M, İçağasioğlu DF, Toker RT, Yilmaz S, Arslan EA, Güngör M, Kutluk G, Erol İ, Mert GG, Polat BG, Aksoy A. Öz Tunçer G, et al. J Neuromuscul Dis. 2023;10(5):915-924. doi: 10.3233/JND-230046. J Neuromuscul Dis. 2023. PMID: 37355912 Free PMC article.
Case report: Incomplete penetrance of autosomal dominant myotonia congenita caused by a rare CLCN1 variant c.1667T>A (p.I556N) in a Malaysian family.
Musa NH, Thilakavathy K, Mohamad NA, Kennerson ML, Inche Mat LN, Loh WC, Abdul Rashid AM, Baharin J, Ibrahim A, Wan Sulaiman WA, Hoo FK, Basri H, Yusof Khan AHK. Musa NH, et al. Front Genet. 2023 Jan 3;13:972007. doi: 10.3389/fgene.2022.972007. eCollection 2022. Front Genet. 2023. PMID: 36659963 Free PMC article.
Value of short exercise and short exercise with cooling tests in diagnosis of recessive form of myotonia congenita (Becker disease) - are sex differences important?
Nojszewska M, Lusakowska A, Gawel M, Sierdzinski J, Sulek A, Krysa W, Elert-Dobkowska E, Seroka A, Kaminska AM, Kostera-Pruszczyk A. Nojszewska M, et al. Neurol Neurochir Pol. 2022;56(5):399-403. doi: 10.5603/PJNNS.a2022.0051. Epub 2022 Jul 6. Neurol Neurochir Pol. 2022. PMID: 35792560 Free article.
500 results