Aylett S - Search Results

1

Genotypic and phenotypic spectrum of pyridoxine-dependent epilepsy (ALDH7A1 deficiency).

Mills PB, Footitt EJ, Mills KA, Tuschl K, Aylett S, Varadkar S, Hemingway C, Marlow N, Rennie J, Baxter P, Dulac O, Nabbout R, Craigen WJ, Schmitt B, Feillet F, Christensen E, De Lonlay P, Pike MG, Hughes MI, Struys EA, Jakobs C, Zuberi SM, Clayton PT. Mills PB, et al. Among authors: aylett s. Brain. 2010 Jul;133(Pt 7):2148-59. doi: 10.1093/brain/awq143. Epub 2010 Jun 16. Brain. 2010. PMID: 20554659 Free PMC article.

2

Homozygous mutations in the SCN1A gene associated with genetic epilepsy with febrile seizures plus and Dravet syndrome in 2 families.

Brunklaus A, Ellis R, Stewart H, Aylett S, Reavey E, Jefferson R, Jain R, Chakraborty S, Jayawant S, Zuberi SM. Brunklaus A, et al. Among authors: aylett s. Eur J Paediatr Neurol. 2015 Jul;19(4):484-8. doi: 10.1016/j.ejpn.2015.02.001. Epub 2015 Feb 21. Eur J Paediatr Neurol. 2015. PMID: 25795284

3

Diagnostic algorithm for children presenting with epilepsia partialis continua.

Surana S, Rossor T, Hassell J, Boyd S, D'Arco F, Aylett S, Bhate S, Carr L, Das K, DeVile C, Eltze C, Hemingway C, Kaliakatsos M, O'Callaghan F, Prabhakar P, Robinson R, Varadkar S, Helen Cross J, Hacohen Y. Surana S, et al. Among authors: aylett s. Epilepsia. 2020 Oct;61(10):2224-2233. doi: 10.1111/epi.16650. Epub 2020 Sep 2. Epilepsia. 2020. PMID: 32875551

4

Pyridoxine-dependent seizures: a family phenotype that leads to severe cognitive deficits, regardless of treatment regime.

Rankin PM, Harrison S, Chong WK, Boyd S, Aylett SE. Rankin PM, et al. Among authors: aylett se. Dev Med Child Neurol. 2007 Apr;49(4):300-5. doi: 10.1111/j.1469-8749.2007.00300.x. Dev Med Child Neurol. 2007. PMID: 17376142 Free article.

5

Faulty cardiac repolarization reserve in alternating hemiplegia of childhood broadens the phenotype.

Jaffer F, Avbersek A, Vavassori R, Fons C, Campistol J, Stagnaro M, De Grandis E, Veneselli E, Rosewich H, Gianotta M, Zucca C, Ragona F, Granata T, Nardocci N, Mikati M, Helseth AR, Boelman C, Minassian BA, Johns S, Garry SI, Scheffer IE, Gourfinkel-An I, Carrilho I, Aylett SE, Parton M, Hanna MG, Houlden H, Neville B, Kurian MA, Novy J, Sander JW, Lambiase PD, Behr ER, Schyns T, Arzimanoglou A, Cross JH, Kaski JP, Sisodiya SM. Jaffer F, et al. Among authors: aylett se. Brain. 2015 Oct;138(Pt 10):2859-74. doi: 10.1093/brain/awv243. Epub 2015 Aug 21. Brain. 2015. PMID: 26297560 Free PMC article.

6

Eye rolling as a manifestation of clobazam toxicity in a child with epilepsy.

Aylett SE, Cross H, Berry D. Aylett SE, et al. Dev Med Child Neurol. 2006 Jul;48(7):612-5. doi: 10.1017/S0012162206001289. Dev Med Child Neurol. 2006. PMID: 16780634 Free article.

7

Features of developmental coordination disorder in active childhood epilepsy: a population-based study.

Reilly C, Atkinson P, Das KB, Chin RF, Aylett SE, Burch V, Gillberg C, Scott RC, Neville BG. Reilly C, et al. Dev Med Child Neurol. 2015 Sep;57(9):829-34. doi: 10.1111/dmcn.12763. Epub 2015 Apr 16. Dev Med Child Neurol. 2015. PMID: 25882788 Free article.

8

Features of autism spectrum disorder (ASD) in childhood epilepsy: a population-based study.

Reilly C, Atkinson P, Das KB, Chin RF, Aylett SE, Burch V, Gillberg C, Scott RC, Neville BG. Reilly C, et al. Epilepsy Behav. 2015 Jan;42:86-92. doi: 10.1016/j.yebeh.2014.11.014. Epub 2014 Dec 16. Epilepsy Behav. 2015. PMID: 25529303

9

Factors associated with quality of life in active childhood epilepsy: a population-based study.

Reilly C, Atkinson P, Das KB, Chin RF, Aylett SE, Burch V, Gillberg C, Scott RC, Neville BG. Reilly C, et al. Eur J Paediatr Neurol. 2015 May;19(3):308-13. doi: 10.1016/j.ejpn.2014.12.022. Epub 2015 Jan 8. Eur J Paediatr Neurol. 2015. PMID: 25596900

10

Epilepsy surgery in children under 3 years.

Dunkley C, Kung J, Scott RC, Nicolaides P, Neville B, Aylett SE, Harkness W, Cross JH. Dunkley C, et al. Among authors: aylett se. Epilepsy Res. 2011 Feb;93(2-3):96-106. doi: 10.1016/j.eplepsyres.2010.11.002. Epub 2010 Dec 14. Epilepsy Res. 2011. PMID: 21156345

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