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

Year Number of Results
1995 1
2000 1
2001 1
2002 1
2006 1
2007 1
2008 2
2010 1
2011 2
2012 3
2013 6
2014 5
2015 2
2016 3
2017 5
2018 4
2019 9
2020 5
2021 6
2022 0
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53 results
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Page 1
Clustering of suicides in children and adolescents.
Hawton K, Hill NTM, Gould M, John A, Lascelles K, Robinson J. Hawton K, et al. Among authors: lascelles k. Lancet Child Adolesc Health. 2020 Jan;4(1):58-67. doi: 10.1016/S2352-4642(19)30335-9. Epub 2019 Oct 9. Lancet Child Adolesc Health. 2020. PMID: 31606323 Review.
The spectrum of intermediate SCN8A-related epilepsy.
Johannesen KM, Gardella E, Encinas AC, Lehesjoki AE, Linnankivi T, Petersen MB, Lund ICB, Blichfeldt S, Miranda MJ, Pal DK, Lascelles K, Procopis P, Orsini A, Bonuccelli A, Giacomini T, Helbig I, Fenger CD, Sisodiya SM, Hernandez-Hernandez L, Krithika S, Rumple M, Masnada S, Valente M, Cereda C, Giordano L, Accorsi P, Bürki SE, Mancardi M, Korff C, Guerrini R, von Spiczak S, Hoffman-Zacharska D, Mazurczak T, Coppola A, Buono S, Vecchi M, Hammer MF, Varesio C, Veggiotti P, Lal D, Brünger T, Zara F, Striano P, Rubboli G, Møller RS. Johannesen KM, et al. Among authors: lascelles k. Epilepsia. 2019 May;60(5):830-844. doi: 10.1111/epi.14705. Epub 2019 Apr 10. Epilepsia. 2019. PMID: 30968951
Phenotypic and genetic spectrum of epilepsy with myoclonic atonic seizures.
Tang S, Addis L, Smith A, Topp SD, Pendziwiat M, Mei D, Parker A, Agrawal S, Hughes E, Lascelles K, Williams RE, Fallon P, Robinson R, Cross HJ, Hedderly T, Eltze C, Kerr T, Desurkar A, Hussain N, Kinali M, Bagnasco I, Vassallo G, Whitehouse W, Goyal S, Absoud M; EuroEPINOMICS-RES Consortium, Møller RS, Helbig I, Weber YG, Marini C, Guerrini R, Simpson MA, Pal DK. Tang S, et al. Among authors: lascelles k. Epilepsia. 2020 May;61(5):995-1007. doi: 10.1111/epi.16508. Epub 2020 May 29. Epilepsia. 2020. PMID: 32469098
Authors' reply.
Gibbons R, Brand F, Carbonnier A, Croft A, Lascelles K, Wolfart G, Hawton K. Gibbons R, et al. Among authors: lascelles k. BJPsych Bull. 2020 Apr;44(2):84. doi: 10.1192/bjb.2020.15. BJPsych Bull. 2020. PMID: 32223787 Free PMC article. No abstract available.
Ischemic Stroke Following Ergotamine Overdose.
Bednarczuk NF, Lim M, Siddiqui A, Lascelles K. Bednarczuk NF, et al. Among authors: lascelles k. Pediatr Neurol. 2019 Dec;101:81-82. doi: 10.1016/j.pediatrneurol.2019.07.016. Epub 2019 Aug 6. Pediatr Neurol. 2019. PMID: 31570294 No abstract available.
Reversible vigabatrin-induced life-threatening encephalopathy.
Hernández Vega Y, Kaliakatsos M, U-King-Im JM, Lascelles K, Lim M. Hernández Vega Y, et al. Among authors: lascelles k. JAMA Neurol. 2014 Jan;71(1):108-9. doi: 10.1001/jamaneurol.2013.1858. JAMA Neurol. 2014. PMID: 24247994 No abstract available.
Encephalopathy and SCN1A mutations.
Tang S, Lin JP, Hughes E, Siddiqui A, Lim M, Lascelles K. Tang S, et al. Among authors: lascelles k. Epilepsia. 2011 Apr;52(4):e26-30. doi: 10.1111/j.1528-1167.2011.03019.x. Epub 2011 Mar 22. Epilepsia. 2011. PMID: 21426328 Free article.
Clinical and molecular characterization of KCNT1-related severe early-onset epilepsy.
McTague A, Nair U, Malhotra S, Meyer E, Trump N, Gazina EV, Papandreou A, Ngoh A, Ackermann S, Ambegaonkar G, Appleton R, Desurkar A, Eltze C, Kneen R, Kumar AV, Lascelles K, Montgomery T, Ramesh V, Samanta R, Scott RH, Tan J, Whitehouse W, Poduri A, Scheffer IE, Chong WKK, Cross JH, Topf M, Petrou S, Kurian MA. McTague A, et al. Among authors: lascelles k. Neurology. 2018 Jan 2;90(1):e55-e66. doi: 10.1212/WNL.0000000000004762. Epub 2017 Dec 1. Neurology. 2018. PMID: 29196579 Free PMC article.
Further refinement of COL4A1 and COL4A2 related cortical malformations.
Cavallin M, Mine M, Philbert M, Boddaert N, Lepage JM, Coste T, Lopez-Gonzalez V, Sanchez-Soler MJ, Ballesta-Martínez MJ, Remerand G, Pasquier L, Guët A, Chelly J, Lascelles K, Prieto-Morin C, Kossorotoff M, Tournier Lasserve E, Bahi-Buisson N. Cavallin M, et al. Among authors: lascelles k. Eur J Med Genet. 2018 Dec;61(12):765-772. doi: 10.1016/j.ejmg.2018.10.004. Epub 2018 Oct 11. Eur J Med Genet. 2018. PMID: 30315939
53 results