Gill DS - Search Results

1

CHD2 myoclonic encephalopathy is frequently associated with self-induced seizures.

Thomas RH, Zhang LM, Carvill GL, Archer JS, Heavin SB, Mandelstam SA, Craiu D, Berkovic SF, Gill DS, Mefford HC, Scheffer IE; EuroEPINOMICS RES Consortium. Thomas RH, et al. Among authors: gill ds. Neurology. 2015 Mar 3;84(9):951-8. doi: 10.1212/WNL.0000000000001305. Epub 2015 Feb 11. Neurology. 2015. PMID: 25672921 Free PMC article.

2

Natural history of cognitive deficits and their relationship to MRI T2-hyperintensities in NF1.

Hyman SL, Gill DS, Shores EA, Steinberg A, Joy P, Gibikote SV, North KN. Hyman SL, et al. Among authors: gill ds. Neurology. 2003 Apr 8;60(7):1139-45. doi: 10.1212/01.wnl.0000055090.78351.c1. Neurology. 2003. PMID: 12682321

3

De-novo mutations of the sodium channel gene SCN1A in alleged vaccine encephalopathy: a retrospective study.

Berkovic SF, Harkin L, McMahon JM, Pelekanos JT, Zuberi SM, Wirrell EC, Gill DS, Iona X, Mulley JC, Scheffer IE. Berkovic SF, et al. Among authors: gill ds. Lancet Neurol. 2006 Jun;5(6):488-92. doi: 10.1016/S1474-4422(06)70446-X. Lancet Neurol. 2006. PMID: 16713920

4

The spectrum of SCN1A-related infantile epileptic encephalopathies.

Harkin LA, McMahon JM, Iona X, Dibbens L, Pelekanos JT, Zuberi SM, Sadleir LG, Andermann E, Gill D, Farrell K, Connolly M, Stanley T, Harbord M, Andermann F, Wang J, Batish SD, Jones JG, Seltzer WK, Gardner A; Infantile Epileptic Encephalopathy Referral Consortium; Sutherland G, Berkovic SF, Mulley JC, Scheffer IE. Harkin LA, et al. Brain. 2007 Mar;130(Pt 3):843-52. doi: 10.1093/brain/awm002. Brain. 2007. PMID: 17347258

5

Epilepsy and mental retardation limited to females with PCDH19 mutations can present de novo or in single generation families.

Hynes K, Tarpey P, Dibbens LM, Bayly MA, Berkovic SF, Smith R, Raisi ZA, Turner SJ, Brown NJ, Desai TD, Haan E, Turner G, Christodoulou J, Leonard H, Gill D, Stratton MR, Gecz J, Scheffer IE. Hynes K, et al. J Med Genet. 2010 Mar;47(3):211-6. doi: 10.1136/jmg.2009.068817. Epub 2009 Sep 14. J Med Genet. 2010. PMID: 19752159

6

Cortical hypometabolism demonstrated by PET in relapsing NMDA receptor encephalitis.

Pillai SC, Gill D, Webster R, Howman-Giles R, Dale RC. Pillai SC, et al. Pediatr Neurol. 2010 Sep;43(3):217-20. doi: 10.1016/j.pediatrneurol.2010.04.019. Pediatr Neurol. 2010. PMID: 20691947

7

VGKC antibodies in pediatric encephalitis presenting with status epilepticus.

Suleiman J, Brenner T, Gill D, Brilot F, Antony J, Vincent A, Lang B, Dale RC. Suleiman J, et al. Neurology. 2011 Apr 5;76(14):1252-5. doi: 10.1212/WNL.0b013e3182143552. Neurology. 2011. PMID: 21464429

8

Immune-mediated steroid-responsive epileptic spasms and epileptic encephalopathy associated with VGKC-complex antibodies.

Suleiman J, Brenner T, Gill D, Troedson C, Sinclair AJ, Brilot F, Vincent A, Lang B, Dale RC. Suleiman J, et al. Dev Med Child Neurol. 2011 Nov;53(11):1058-60. doi: 10.1111/j.1469-8749.2011.04096.x. Epub 2011 Aug 30. Dev Med Child Neurol. 2011. PMID: 21883173 Free article.

9

Rare copy number variants are an important cause of epileptic encephalopathies.

Mefford HC, Yendle SC, Hsu C, Cook J, Geraghty E, McMahon JM, Eeg-Olofsson O, Sadleir LG, Gill D, Ben-Zeev B, Lerman-Sagie T, Mackay M, Freeman JL, Andermann E, Pelakanos JT, Andrews I, Wallace G, Eichler EE, Berkovic SF, Scheffer IE. Mefford HC, et al. Ann Neurol. 2011 Dec;70(6):974-85. doi: 10.1002/ana.22645. Ann Neurol. 2011. PMID: 22190369 Free PMC article.

10

Febrile infection-related epilepsy syndrome is not caused by SCN1A mutations.

Carranza Rojo D, Harvey AS, Iona X, Dibbens LM, Damiano JA, Arsov T, Gill D, Freeman JL, Leventer RJ, Vincent A, Berkovic SF, McMahon JM, Scheffer IE. Carranza Rojo D, et al. Epilepsy Res. 2012 Jun;100(1-2):194-8. doi: 10.1016/j.eplepsyres.2012.02.007. Epub 2012 Mar 3. Epilepsy Res. 2012. PMID: 22386634

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