Makoff A - Search Results

1

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: makoff a. 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.

2

A case report of a family with overlapping features of autosomal dominant febrile seizures and GEFS+.

Hindocha N, Nabbout R, Elmslie F, Makoff A, Al-Chalabi A, Nashef L. Hindocha N, et al. Among authors: makoff a. Epilepsia. 2009 Apr;50(4):937-42. doi: 10.1111/j.1528-1167.2008.01876.x. Epub 2008 Nov 19. Epilepsia. 2009. PMID: 19054398 Free article.

3

Risk factors in sudden death in epilepsy (SUDEP): the quest for mechanisms.

Nashef L, Hindocha N, Makoff A. Nashef L, et al. Among authors: makoff a. Epilepsia. 2007 May;48(5):859-71. doi: 10.1111/j.1528-1167.2007.01082.x. Epub 2007 Apr 13. Epilepsia. 2007. PMID: 17433051 Free article. Review.

4

High-density SNP screen of sodium channel genes by haplotype tagging and DNA pooling for association with idiopathic generalized epilepsy.

Makoff A, Lai T, Barratt C, Valentin A, Moran N, Asherson P, Nashef L. Makoff A, et al. Epilepsia. 2010 Apr;51(4):694-8. doi: 10.1111/j.1528-1167.2009.02473.x. Epub 2009 Dec 22. Epilepsia. 2010. PMID: 20041941 Free article.

5

Idiopathic generalized epilepsy with absences: syndrome classification.

Valentin A, Hindocha N, Osei-Lah A, Fisniku L, McCormick D, Asherson P, Moran N, Makoff A, Nashef L. Valentin A, et al. Among authors: makoff a. Epilepsia. 2007 Nov;48(11):2187-90. doi: 10.1111/j.1528-1167.2007.01226.x. Epub 2007 Jul 30. Epilepsia. 2007. PMID: 17666074 Free article.

6

No association of single nucleotide polymorphisms in the micro-opioid receptor subunit gene with idiopathic generalized epilepsy.

Barratt C, Lai T, Nashef L, Valentin A, Fisniku L, Moran N, Asherson P, Makoff A. Barratt C, et al. Among authors: makoff a. Epilepsia. 2006 Oct;47(10):1728-31. doi: 10.1111/j.1528-1167.2006.00844.x. Epilepsia. 2006. PMID: 17054695 Free article.

7

CACNA1A and P/Q-type calcium channels in epilepsy.

Chioza B, Nashef L, Asherson P, Makoff A. Chioza B, et al. Among authors: makoff a. Lancet. 2002 Jan 19;359(9302):258. doi: 10.1016/S0140-6736(02)07416-0. Lancet. 2002. PMID: 11812585 No abstract available.

8

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: makoff a. Epileptic Disord. 2007 Jun;9(2):194-236. doi: 10.1684/epd.2007.0107. Epileptic Disord. 2007. PMID: 17525034 Free article.

9

Suggestive evidence for association of two potassium channel genes with different idiopathic generalised epilepsy syndromes.

Chioza B, Osei-Lah A, Wilkie H, Nashef L, McCormick D, Asherson P, Makoff AJ. Chioza B, et al. Among authors: makoff aj. Epilepsy Res. 2002 Dec;52(2):107-16. doi: 10.1016/s0920-1211(02)00195-x. Epilepsy Res. 2002. PMID: 12458027

10

Haplotype and linkage disequilibrium analysis to characterise a region in the calcium channel gene CACNA1A associated with idiopathic generalised epilepsy.

Chioza B, Osei-Lah A, Nashef L, Suarez-Merino B, Wilkie H, Sham P, Knight J, Asherson P, Makoff AJ. Chioza B, et al. Among authors: makoff aj. Eur J Hum Genet. 2002 Dec;10(12):857-64. doi: 10.1038/sj.ejhg.5200896. Eur J Hum Genet. 2002. PMID: 12461694

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