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

Year Number of Results
1991 1
1995 2
1997 2
1998 5
1999 2
2003 1
2004 1
2005 16
2006 19
2007 11
2008 14
2009 15
2010 11
2011 9
2012 8
2013 8
2014 7
2015 13
2016 9
2017 6
2018 2
2019 5
2020 6
2021 1
2022 4
2023 2
2024 0

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Similar articles for PMID: 15689435

155 results

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Page 1
MECP2 mutations in Serbian Rett syndrome patients.
Djarmati A, Dobricić V, Kecmanović M, Marsh P, Jancić-Stefanović J, Klein C, Djurić M, Romac S. Djarmati A, et al. Acta Neurol Scand. 2007 Dec;116(6):413-9. doi: 10.1111/j.1600-0404.2007.00893.x. Acta Neurol Scand. 2007. PMID: 17986102
Gene symbol: MECP2. Disease: Rett syndrome (atypical).
Penagarikano O, Martinez-Bouzas C, Mínguez M, Sanz-Parra A, García-Alegría E, Beristain E, Tejada MI. Penagarikano O, et al. Hum Genet. 2005 Dec;118(3-4):547. Hum Genet. 2005. PMID: 16521306 No abstract available.
Rett syndrome: from the gene to the disease.
Matijevic T, Knezevic J, Slavica M, Pavelic J. Matijevic T, et al. Eur Neurol. 2009;61(1):3-10. doi: 10.1159/000165342. Epub 2008 Oct 24. Eur Neurol. 2009. PMID: 18948693 Free article. Review.
155 results