King MD - Search Results

1

Chromosomal microarray in unexplained severe early onset epilepsy - A single centre cohort.

Allen NM, Conroy J, Shahwan A, Ennis S, Lynch B, Lynch SA, King MD. Allen NM, et al. Among authors: king md. Eur J Paediatr Neurol. 2015 Jul;19(4):390-4. doi: 10.1016/j.ejpn.2015.03.010. Epub 2015 Apr 10. Eur J Paediatr Neurol. 2015. PMID: 25920948

2

Unexplained early onset epileptic encephalopathy: Exome screening and phenotype expansion.

Allen NM, Conroy J, Shahwan A, Lynch B, Correa RG, Pena SD, McCreary D, Magalhães TR, Ennis S, Lynch SA, King MD. Allen NM, et al. Among authors: king md. Epilepsia. 2016 Jan;57(1):e12-7. doi: 10.1111/epi.13250. Epub 2015 Dec 9. Epilepsia. 2016. PMID: 26648591 Free article.

3

Status dystonicus due to missense variant in ARX: Diagnosis and management.

Gorman KM, Cary H, Gaffney L, Forman E, Waldron D, Al-Delami F, Lynch BJ, King MD, Allen NM. Gorman KM, et al. Among authors: king md. Eur J Paediatr Neurol. 2018 Sep;22(5):862-865. doi: 10.1016/j.ejpn.2018.04.015. Epub 2018 May 3. Eur J Paediatr Neurol. 2018. PMID: 29778428

4

Partial status epilepticus - rapid genetic diagnosis of Alpers' disease.

McCoy B, Owens C, Howley R, Ryan S, King M, Farrell MA, Lynch BJ. McCoy B, et al. Eur J Paediatr Neurol. 2011 Nov;15(6):558-62. doi: 10.1016/j.ejpn.2011.05.012. Epub 2011 Jun 24. Eur J Paediatr Neurol. 2011. PMID: 21704543

5

Excellent outcome with de novo 15q13.3 microdeletion causing infantile spasms--a further patient.

Allen NM, Conroy J, Shahwan A, Ennis S, Lynch B, Lynch SA, King MD. Allen NM, et al. Among authors: king md. Am J Med Genet A. 2014 Jul;164A(7):1863-6. doi: 10.1002/ajmg.a.36532. Epub 2014 Apr 3. Am J Med Genet A. 2014. PMID: 24700477 No abstract available.

6

Towards the identification of a genetic basis for Landau-Kleffner syndrome.

Conroy J, McGettigan PA, McCreary D, Shah N, Collins K, Parry-Fielder B, Moran M, Hanrahan D, Deonna TW, Korff CM, Webb D, Ennis S, Lynch SA, King MD. Conroy J, et al. Among authors: king md. Epilepsia. 2014 Jun;55(6):858-65. doi: 10.1111/epi.12645. Epub 2014 May 14. Epilepsia. 2014. PMID: 24828792 Free article.

7

The variable phenotypes of KCNQ-related epilepsy.

Allen NM, Mannion M, Conroy J, Lynch SA, Shahwan A, Lynch B, King MD. Allen NM, et al. Among authors: king md. Epilepsia. 2014 Sep;55(9):e99-105. doi: 10.1111/epi.12715. Epub 2014 Jul 22. Epilepsia. 2014. PMID: 25052858 Free article.

8

Epilepsy surgery in pediatric epileptic encephalopathy: when interictal EEG counts the most.

Shahwan A, O'Halloran PJ, Madigan C, King MD, O'Brien D. Shahwan A, et al. Among authors: king md. Childs Nerv Syst. 2016 Jul;32(7):1293-8. doi: 10.1007/s00381-016-3104-4. Epub 2016 May 14. Childs Nerv Syst. 2016. PMID: 27179532

9

Novel European SLC1A4 variant: infantile spasms and population ancestry analysis.

Conroy J, Allen NM, Gorman K, O'Halloran E, Shahwan A, Lynch B, Lynch SA, Ennis S, King MD. Conroy J, et al. Among authors: king md. J Hum Genet. 2016 Aug;61(8):761-4. doi: 10.1038/jhg.2016.44. Epub 2016 May 19. J Hum Genet. 2016. PMID: 27193218

10

Atypical benign partial epilepsy of childhood with acquired neurocognitive, lexical semantic, and autistic spectrum disorder.

Allen NM, Conroy J, Deonna T, McCreary D, McGettigan P, Madigan C, Carter I, Ennis S, Lynch SA, Shahwan A, King MD. Allen NM, et al. Among authors: king md. Epilepsy Behav Case Rep. 2016 Apr 23;6:42-8. doi: 10.1016/j.ebcr.2016.04.003. eCollection 2016. Epilepsy Behav Case Rep. 2016. PMID: 27504264 Free PMC article.

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