Zuberi SM - Search Results

1

Dravet syndrome and its mimics: Beyond SCN1A.

Steel D, Symonds JD, Zuberi SM, Brunklaus A. Steel D, et al. Among authors: zuberi sm. Epilepsia. 2017 Nov;58(11):1807-1816. doi: 10.1111/epi.13889. Epub 2017 Sep 7. Epilepsia. 2017. PMID: 28880996 Review.

2

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. Among authors: zuberi sm. Brain. 2007 Mar;130(Pt 3):843-52. doi: 10.1093/brain/awm002. Brain. 2007. PMID: 17347258

3

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. 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.

4

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. Among authors: zuberi sm. J Child Neurol. 2009 Apr;24(4):503-8. doi: 10.1177/0883073808324537. J Child Neurol. 2009. PMID: 19339291

5

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. Among authors: zuberi sm. 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

6

Genotype-phenotype associations in SCN1A-related epilepsies.

Zuberi SM, Brunklaus A, Birch R, Reavey E, Duncan J, Forbes GH. Zuberi SM, et al. Neurology. 2011 Feb 15;76(7):594-600. doi: 10.1212/WNL.0b013e31820c309b. Epub 2011 Jan 19. Neurology. 2011. PMID: 21248271

7

Investigating neuroblastoma in childhood opsoclonus-myoclonus syndrome.

Brunklaus A, Pohl K, Zuberi SM, de Sousa C. Brunklaus A, et al. Among authors: zuberi sm. Arch Dis Child. 2012 May;97(5):461-3. doi: 10.1136/adc.2010.204792. Epub 2011 Apr 3. Arch Dis Child. 2012. PMID: 21460401

8

Comorbidities and predictors of health-related quality of life in Dravet syndrome.

Brunklaus A, Dorris L, Zuberi SM. Brunklaus A, et al. Among authors: zuberi sm. Epilepsia. 2011 Aug;52(8):1476-82. doi: 10.1111/j.1528-1167.2011.03129.x. Epub 2011 Jun 10. Epilepsia. 2011. PMID: 21668444 Free article.

9

Outcome and prognostic features in opsoclonus-myoclonus syndrome from infancy to adult life.

Brunklaus A, Pohl K, Zuberi SM, de Sousa C. Brunklaus A, et al. Among authors: zuberi sm. Pediatrics. 2011 Aug;128(2):e388-94. doi: 10.1542/peds.2010-3114. Epub 2011 Jul 25. Pediatrics. 2011. PMID: 21788225

10

Prognostic, clinical and demographic features in SCN1A mutation-positive Dravet syndrome.

Brunklaus A, Ellis R, Reavey E, Forbes GH, Zuberi SM. Brunklaus A, et al. Among authors: zuberi sm. Brain. 2012 Aug;135(Pt 8):2329-36. doi: 10.1093/brain/aws151. Epub 2012 Jun 19. Brain. 2012. PMID: 22719002

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