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

Year Number of Results
1950 2
1951 1
1955 3
1956 1
1960 1
1962 1
1963 1
1966 1
1968 1
1969 2
1970 1
1978 1
1979 1
1980 1
1984 2
1987 1
1988 2
1989 3
1990 1
1991 3
1994 1
1995 2
1998 3
1999 4
2000 2
2001 2
2002 1
2003 4
2004 2
2005 5
2006 10
2007 3
2008 8
2009 9
2010 11
2011 12
2012 27
2013 19
2014 21
2015 15
2016 9
2017 9
2018 8
2019 9
2020 13
2021 8
2022 8
2023 1
2024 0

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Similar articles for PMID: 22578097

227 results

Results by year

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Page 1
Electroclinical pattern in MECP2 duplication syndrome: eight new reported cases and review of literature.
Vignoli A, Borgatti R, Peron A, Zucca C, Ballarati L, Bonaglia C, Bellini M, Giordano L, Romaniello R, Bedeschi MF, Epifanio R, Russo S, Caselli R, Giardino D, Darra F, La Briola F, Banderali G, Canevini MP. Vignoli A, et al. Epilepsia. 2012 Jul;53(7):1146-55. doi: 10.1111/j.1528-1167.2012.03501.x. Epub 2012 May 11. Epilepsia. 2012. PMID: 22578097 Free article. Review.
Neurologic aspects of MECP2 gene duplication in male patients.
Echenne B, Roubertie A, Lugtenberg D, Kleefstra T, Hamel BC, Van Bokhoven H, Lacombe D, Philippe C, Jonveaux P, de Brouwer AP. Echenne B, et al. Pediatr Neurol. 2009 Sep;41(3):187-91. doi: 10.1016/j.pediatrneurol.2009.03.012. Pediatr Neurol. 2009. PMID: 19664534
Structural variation in Xq28: MECP2 duplications in 1% of patients with unexplained XLMR and in 2% of male patients with severe encephalopathy.
Lugtenberg D, Kleefstra T, Oudakker AR, Nillesen WM, Yntema HG, Tzschach A, Raynaud M, Rating D, Journel H, Chelly J, Goizet C, Lacombe D, Pedespan JM, Echenne B, Tariverdian G, O'Rourke D, King MD, Green A, van Kogelenberg M, Van Esch H, Gecz J, Hamel BC, van Bokhoven H, de Brouwer AP. Lugtenberg D, et al. Eur J Hum Genet. 2009 Apr;17(4):444-53. doi: 10.1038/ejhg.2008.208. Epub 2008 Nov 5. Eur J Hum Genet. 2009. PMID: 18985075 Free PMC article.
227 results