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Year Number of Results
1953 2
1954 1
1979 2
1992 1
1993 2
1995 4
1996 2
1998 2
1999 1
2000 1
2002 1
2004 2
2007 4
2008 1
2009 2
2010 2
2011 2
2012 2
2013 3
2014 1
2019 1
2020 1
2022 1
2024 3
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40 results

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Page 1
Expanding the Mutational Landscape and Clinical Phenotype of CHD2-Related Encephalopathy.
Clara-Hwang A, Stefani S, Lau T, Scala M, Aynekin B, Bernardo P, Madia F, Bakhtadze S, Kaiyrzhanov R, Maroofian R, Zara F, Srinivasan VM, Gowda V, Guliyeva U, Montavont A, Poulat AL, Güleç A, Berger C, Ville DM, de Bellescize J, Cabet S, Wonneberger A, Schulz A, Rodriguez-Palmero A, Chatron N, Lesca G, Per H, Goel H, Brown J, Frey T, Steindl K, Rauch A, Severino M, Houlden H, Nicolaides P, Striano P, Efthymiou S. Clara-Hwang A, et al. Among authors: nicolaides p. Neurol Genet. 2024 Jul 11;10(4):e200168. doi: 10.1212/NXG.0000000000200168. eCollection 2024 Aug. Neurol Genet. 2024. PMID: 39035822 Free PMC article.
The SANAD study of effectiveness of valproate, lamotrigine, or topiramate for generalised and unclassifiable epilepsy: an unblinded randomised controlled trial.
Marson AG, Al-Kharusi AM, Alwaidh M, Appleton R, Baker GA, Chadwick DW, Cramp C, Cockerell OC, Cooper PN, Doughty J, Eaton B, Gamble C, Goulding PJ, Howell SJ, Hughes A, Jackson M, Jacoby A, Kellett M, Lawson GR, Leach JP, Nicolaides P, Roberts R, Shackley P, Shen J, Smith DF, Smith PE, Smith CT, Vanoli A, Williamson PR; SANAD Study group. Marson AG, et al. Among authors: nicolaides p. Lancet. 2007 Mar 24;369(9566):1016-26. doi: 10.1016/S0140-6736(07)60461-9. Lancet. 2007. PMID: 17382828 Free PMC article. Clinical Trial.
Delayed diagnosis of Duchenne muscular dystrophy.
Mohamed K, Appleton R, Nicolaides P. Mohamed K, et al. Among authors: nicolaides p. Eur J Paediatr Neurol. 2000;4(5):219-23. doi: 10.1053/ejpn.2000.0309. Eur J Paediatr Neurol. 2000. PMID: 11030068 Review.
Non-disjunction of chromosome 18.
Bugge M, Collins A, Petersen MB, Fisher J, Brandt C, Hertz JM, Tranebjaerg L, de Lozier-Blanchet C, Nicolaides P, Brøndum-Nielsen K, Morton N, Mikkelsen M. Bugge M, et al. Among authors: nicolaides p. Hum Mol Genet. 1998 Apr;7(4):661-9. doi: 10.1093/hmg/7.4.661. Hum Mol Genet. 1998. PMID: 9499419
Tetrasomy 9p mosaicism associated with a normal phenotype in two cases.
Papoulidis I, Kontodiou M, Tzimina M, Saitis I, Hamid AB, Klein E, Kosyakova N, Kordass U, Kunz J, Siomou E, Nicolaides P, Orru S, Thomaidis L, Liehr T, Petersen MB, Manolakos E. Papoulidis I, et al. Among authors: nicolaides p. Cytogenet Genome Res. 2012;136(4):237-41. doi: 10.1159/000337520. Epub 2012 Apr 5. Cytogenet Genome Res. 2012. PMID: 22487875 Review.
Stroke in children.
Nicolaides P, Appleton RE. Nicolaides P, et al. Dev Med Child Neurol. 1996 Feb;38(2):172-80. doi: 10.1111/j.1469-8749.1996.tb12090.x. Dev Med Child Neurol. 1996. PMID: 8603785 Review. No abstract available.
Early diagnosis of Duchenne muscular dystrophy.
Appleton RE, Nicolaides P. Appleton RE, et al. Among authors: nicolaides p. Lancet. 1995 May 13;345(8959):1243-4. doi: 10.1016/s0140-6736(95)92029-3. Lancet. 1995. PMID: 7739330 No abstract available.
40 results