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2,012 results
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Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder.
Brain. 2010 Mar;133(Pt 3):655-70. doi: 10.1093/brain/awp336. Epub 2010 Feb 2.
Brain. 2010.
PMID: 20129935
Refractory absence epilepsy associated with GLUT-1 deficiency syndrome.
Byrne S, Kearns J, Carolan R, Mc Menamin J, Klepper J, Webb D.
Byrne S, et al. Among authors: webb d.
Epilepsia. 2011 May;52(5):1021-4. doi: 10.1111/j.1528-1167.2011.02989.x. Epub 2011 Mar 2.
Epilepsia. 2011.
PMID: 21366555
Free article.
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Bannayan-Riley-Ruvalcaba syndrome: a cause of extreme macrocephaly and neurodevelopmental delay.
Lynch NE, Lynch SA, McMenamin J, Webb D.
Lynch NE, et al. Among authors: webb d.
Arch Dis Child. 2009 Jul;94(7):553-4. doi: 10.1136/adc.2008.155663. Epub 2009 Mar 25.
Arch Dis Child. 2009.
PMID: 19321504
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Frey syndrome in neurofibromatosis 1.
Ibrahim LF, Brenner C, McMenamin J, Webb D.
Ibrahim LF, et al. Among authors: webb d.
BMJ Case Rep. 2011 Mar 15;2011:bcr0920092286. doi: 10.1136/bcr.09.2009.2286.
BMJ Case Rep. 2011.
PMID: 22698902
Free PMC article.
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Childhood stroke following varicella infection.
Tiah AL, Phelan E, McMenamin J, Webb D.
Tiah AL, et al. Among authors: webb d.
Ir Med J. 2004 Apr;97(4):120-1.
Ir Med J. 2004.
PMID: 15200225
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Audit of the management of convulsive status epilepticus in children: the need for a uniform treatment strategy.
Najam Y, McDonald DG, Keegan M, Webb DW, McMenamin JB.
Najam Y, et al. Among authors: webb dw.
Ir Med J. 2004 Sep;97(8):246-8.
Ir Med J. 2004.
PMID: 15532973
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Acute demyelinating events with rhombencephalitis: a high-risk subgroup in children.
Tirupathi S, Lynch N, Phelan E, Mc Menamin J, Webb D.
Tirupathi S, et al. Among authors: webb d.
Eur J Paediatr Neurol. 2008 Mar;12(2):137-40. doi: 10.1016/j.ejpn.2007.07.004. Epub 2007 Sep 25.
Eur J Paediatr Neurol. 2008.
PMID: 17897850
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PANDAS (Paediatric Autoimmune Neuropsychiatric Disorder Associated with Streptococcal Infection).
Lynch NE, Deiratany S, Webb DW, McMenamin JB.
Lynch NE, et al. Among authors: webb dw.
Ir Med J. 2006 May;99(5):155.
Ir Med J. 2006.
PMID: 16892924
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A comparison of genomic diagnostics in adults and children with epilepsy and comorbid intellectual disability.
Benson KA, White M, Allen NM, Byrne S, Carton R, Comerford E, Costello D, Doherty C, Dunleavey B, El-Naggar H, Gangadharan N, Heavin S, Kearney H, Lench NJ, Lynch J, McCormack M, Regan MO, Podesta K, Power K, Rogers AS, Steward CA, Sweeney B, Webb D, Fitzsimons M, Greally M, Delanty N, Cavalleri GL.
Benson KA, et al. Among authors: webb d.
Eur J Hum Genet. 2020 Aug;28(8):1066-1077. doi: 10.1038/s41431-020-0610-3. Epub 2020 Apr 1.
Eur J Hum Genet. 2020.
PMID: 32238909
Free PMC article.
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Towards the identification of a genetic basis for Landau-Kleffner syndrome.
Conroy J, McGettigan PA, McCreary D, Shah N, Collins K, Parry-Fielder B, Moran M, Hanrahan D, Deonna TW, Korff CM, Webb D, Ennis S, Lynch SA, King MD.
Conroy J, et al. Among authors: webb d.
Epilepsia. 2014 Jun;55(6):858-65. doi: 10.1111/epi.12645. Epub 2014 May 14.
Epilepsia. 2014.
PMID: 24828792
Free article.
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