Similar articles for PMID: 16015284

Year	Number of Results
1998	1
2000	1
2001	5
2002	1
2004	2
2005	10
2006	10
2007	10
2008	8
2009	17
2010	15
2011	19
2012	25
2013	15
2014	10
2015	19
2016	18
2017	15
2018	16
2019	15
2020	8
2021	3
2022	6
2023	2
2024	1

1

Early onset seizures and Rett-like features associated with mutations in CDKL5.

Evans JC, Archer HL, Colley JP, Ravn K, Nielsen JB, Kerr A, Williams E, Christodoulou J, Gécz J, Jardine PE, Wright MJ, Pilz DT, Lazarou L, Cooper DN, Sampson JR, Butler R, Whatley SD, Clarke AJ. Evans JC, et al. Eur J Hum Genet. 2005 Oct;13(10):1113-20. doi: 10.1038/sj.ejhg.5201451. Eur J Hum Genet. 2005. PMID: 16015284

2

Key clinical features to identify girls with CDKL5 mutations.

Bahi-Buisson N, Nectoux J, Rosas-Vargas H, Milh M, Boddaert N, Girard B, Cances C, Ville D, Afenjar A, Rio M, Héron D, N'guyen Morel MA, Arzimanoglou A, Philippe C, Jonveaux P, Chelly J, Bienvenu T. Bahi-Buisson N, et al. Brain. 2008 Oct;131(Pt 10):2647-61. doi: 10.1093/brain/awn197. Epub 2008 Sep 12. Brain. 2008. PMID: 18790821

3

CDKL5 and ARX mutations are not responsible for early onset severe myoclonic epilepsy in infancy.

Nabbout R, Depienne C, Chipaux M, Girard B, Souville I, Trouillard O, Dulac O, Chelly J, Afenjar A, Héron D, Leguern E, Beldjord C, Bienvenu T, Bahi-Buisson N. Nabbout R, et al. Epilepsy Res. 2009 Nov;87(1):25-30. doi: 10.1016/j.eplepsyres.2009.07.004. Epub 2009 Sep 5. Epilepsy Res. 2009. PMID: 19734009

4

Analysis of Hungarian patients with Rett syndrome phenotype for MECP2, CDKL5 and FOXG1 gene mutations.

Hadzsiev K, Polgar N, Bene J, Komlosi K, Karteszi J, Hollody K, Kosztolanyi G, Renieri A, Melegh B. Hadzsiev K, et al. J Hum Genet. 2011 Mar;56(3):183-7. doi: 10.1038/jhg.2010.156. Epub 2010 Dec 16. J Hum Genet. 2011. PMID: 21160487

5

Mutational spectrum of CDKL5 in early-onset encephalopathies: a study of a large collection of French patients and review of the literature.

Nemos C, Lambert L, Giuliano F, Doray B, Roubertie A, Goldenberg A, Delobel B, Layet V, N'guyen MA, Saunier A, Verneau F, Jonveaux P, Philippe C. Nemos C, et al. Clin Genet. 2009 Oct;76(4):357-71. doi: 10.1111/j.1399-0004.2009.01194.x. Clin Genet. 2009. PMID: 19793311 Review.

6

Epilepsy in Rett syndrome---the experience of a National Rett Center.

Nissenkorn A, Gak E, Vecsler M, Reznik H, Menascu S, Ben Zeev B. Nissenkorn A, et al. Epilepsia. 2010 Jul;51(7):1252-8. doi: 10.1111/j.1528-1167.2010.02597.x. Epub 2010 May 13. Epilepsia. 2010. PMID: 20491871 Free article.

7

A novel p.Arg970X mutation in the last exon of the CDKL5 gene resulting in late-onset seizure disorder.

Psoni S, Willems PJ, Kanavakis E, Mavrou A, Frissyra H, Traeger-Synodinos J, Sofokleous C, Makrythanassis P, Kitsiou-Tzeli S. Psoni S, et al. Eur J Paediatr Neurol. 2010 Mar;14(2):188-91. doi: 10.1016/j.ejpn.2009.03.006. Epub 2009 May 9. Eur J Paediatr Neurol. 2010. PMID: 19428276

8

A girl with early-onset epileptic encephalopathy associated with microdeletion involving CDKL5.

Saitsu H, Osaka H, Nishiyama K, Tsurusaki Y, Doi H, Miyake N, Matsumoto N. Saitsu H, et al. Brain Dev. 2012 May;34(5):364-7. doi: 10.1016/j.braindev.2011.07.004. Epub 2011 Jul 28. Brain Dev. 2012. PMID: 21802232

9

Clinical and electroencephalographic features in patients with CDKL5 mutations: two new Italian cases and review of the literature.

Pintaudi M, Baglietto MG, Gaggero R, Parodi E, Pessagno A, Marchi M, Russo S, Veneselli E. Pintaudi M, et al. Epilepsy Behav. 2008 Feb;12(2):326-31. doi: 10.1016/j.yebeh.2007.10.010. Epub 2007 Dec 11. Epilepsy Behav. 2008. PMID: 18063413 Review.

10

Early infantile onset ''congenital'' Rett syndrome variants: Swedish experience through four decades and mutation analysis.

Rajaei S, Erlandson A, Kyllerman M, Albage M, Lundstrom I, Karrstedt EL, Hagberg B. Rajaei S, et al. J Child Neurol. 2011 Jan;26(1):65-71. doi: 10.1177/0883073810374125. J Child Neurol. 2011. PMID: 21212452

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

210 results

Results by year