Zuberi S - Search Results

1

Genetics of epilepsy: epilepsy research foundation workshop report.

Sisodiya S, Cross JH, Blümcke I, Chadwick D, Craig J, Crino PB, Debenham P, Delanty N, Elmslie F, Gardiner M, Golden J, Goldstein D, Greenberg DA, Guerrini R, Hanna M, Harris J, Harrison P, Johnson MR, Kirov G, Kullman DM, Makoff A, Marini C, Nabbout R, Nashef L, Noebels JL, Ottman R, Pirmohamed M, Pitkänen A, Scheffer I, Shorvon S, Sills G, Wood N, Zuberi S. Sisodiya S, et al. Among authors: zuberi s. Epileptic Disord. 2007 Jun;9(2):194-236. doi: 10.1684/epd.2007.0107. Epileptic Disord. 2007. PMID: 17525034 Free article.

2

Ion channels and neurology.

Zuberi SM, Hanna MG. Zuberi SM, et al. Arch Dis Child. 2001 Mar;84(3):277-80. doi: 10.1136/adc.84.3.277. Arch Dis Child. 2001. PMID: 11207185 Free PMC article. Review. No abstract available.

3

Anoxic-epileptic seizures: home video recordings of epileptic seizures induced by syncopes.

Stephenson J, Breningstall G, Steer C, Kirkpatrick M, Horrocks I, Nechay A, Zuberi S. Stephenson J, et al. Among authors: zuberi s. Epileptic Disord. 2004 Mar;6(1):15-9. Epileptic Disord. 2004. PMID: 15075063 Free article.

4

Symptoms of narcolepsy in children misinterpreted as epilepsy.

Macleod S, Ferrie C, Zuberi SM. Macleod S, et al. Among authors: zuberi sm. Epileptic Disord. 2005 Mar;7(1):13-7. Epileptic Disord. 2005. PMID: 15741135 Free article.

5

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: zuberi sm. Lancet Neurol. 2006 Jun;5(6):488-92. doi: 10.1016/S1474-4422(06)70446-X. Lancet Neurol. 2006. PMID: 16713920

6

Two cases of sudden unexpected death in epilepsy in a GEFS+ family with an SCN1A mutation.

Hindocha N, Nashef L, Elmslie F, Birch R, Zuberi S, Al-Chalabi A, Crotti L, Schwartz PJ, Makoff A. Hindocha N, et al. Among authors: zuberi s. Epilepsia. 2008 Feb;49(2):360-5. doi: 10.1111/j.1528-1167.2007.01439_2.x. Epilepsia. 2008. PMID: 18251839 Free article. No abstract available.

7

A novel inherited mutation in the voltage sensor region of SCN1A is associated with Panayiotopoulos syndrome in siblings and generalized epilepsy with febrile seizures plus.

Livingston JH, Cross JH, Mclellan A, Birch R, Zuberi SM. Livingston JH, et al. J Child Neurol. 2009 Apr;24(4):503-8. doi: 10.1177/0883073808324537. J Child Neurol. 2009. PMID: 19339291

8

De novo SCN1A mutations in Dravet syndrome and related epileptic encephalopathies are largely of paternal origin.

Heron SE, Scheffer IE, Iona X, Zuberi SM, Birch R, McMahon JM, Bruce CM, Berkovic SF, Mulley JC. Heron SE, et al. J Med Genet. 2010 Feb;47(2):137-41. doi: 10.1136/jmg.2008.065912. Epub 2009 Jul 8. J Med Genet. 2010. PMID: 19589774

9

Nongenetic factors influence severity of episodic ataxia type 1 in monozygotic twins.

Graves TD, Rajakulendran S, Zuberi SM, Morris HR, Schorge S, Hanna MG, Kullmann DM. Graves TD, et al. Among authors: zuberi sm. Neurology. 2010 Jul 27;75(4):367-72. doi: 10.1212/WNL.0b013e3181ea9ee3. Neurology. 2010. PMID: 20660867 Free PMC article.

10

Dravet syndrome as epileptic encephalopathy: evidence from long-term course and neuropathology.

Catarino CB, Liu JY, Liagkouras I, Gibbons VS, Labrum RW, Ellis R, Woodward C, Davis MB, Smith SJ, Cross JH, Appleton RE, Yendle SC, McMahon JM, Bellows ST, Jacques TS, Zuberi SM, Koepp MJ, Martinian L, Scheffer IE, Thom M, Sisodiya SM. Catarino CB, et al. Among authors: zuberi sm. Brain. 2011 Oct;134(Pt 10):2982-3010. doi: 10.1093/brain/awr129. Epub 2011 Jun 29. Brain. 2011. PMID: 21719429 Free PMC article.

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