Byrne S - Search Results

1

The Temple Star Transitional Model of Care for epilepsy; the outcome of a quality improvement project.

Crowley SL, Byrne S, McNulty S, Keating K, Nestor T, Owen Y, O'Rourke D, Lynch B, Shahwan A, King MD. Crowley SL, et al. Among authors: byrne s. Epilepsy Behav. 2018 Feb;79:4-8. doi: 10.1016/j.yebeh.2017.10.043. Epub 2017 Dec 7. Epilepsy Behav. 2018. PMID: 29223006

2

Does early treatment improve outcomes in N-methyl-D-aspartate receptor encephalitis?

Byrne S, McCoy B, Lynch B, Webb D, King MD. Byrne S, et al. Dev Med Child Neurol. 2014 Aug;56(8):794-6. doi: 10.1111/dmcn.12411. Epub 2014 Mar 19. Dev Med Child Neurol. 2014. PMID: 24641688 Free article.

3

Earlier treatment of NMDAR antibody encephalitis in children results in a better outcome.

Byrne S, Walsh C, Hacohen Y, Muscal E, Jankovic J, Stocco A, Dale RC, Vincent A, Lim M, King M. Byrne S, et al. Neurol Neuroimmunol Neuroinflamm. 2015 Jul 23;2(4):e130. doi: 10.1212/NXI.0000000000000130. eCollection 2015 Aug. Neurol Neuroimmunol Neuroinflamm. 2015. PMID: 26236759 Free PMC article. No abstract available.

4

Catatonic features in children and adolescents with N-methyl-d-aspartate receptor antibody encephalitis.

Eyre M, Kaushik A, Barrett E, King MD, Pollak T, Dale RC, Byrne S, Lim M. Eyre M, et al. Among authors: byrne s. BJPsych Open. 2020 Jul 6;6(4):e71. doi: 10.1192/bjo.2020.55. BJPsych Open. 2020. PMID: 38424748 Free PMC article.

5

Refractory absence epilepsy associated with GLUT-1 deficiency syndrome.

Byrne S, Kearns J, Carolan R, Mc Menamin J, Klepper J, Webb D. Byrne S, et al. Epilepsia. 2011 May;52(5):1021-4. doi: 10.1111/j.1528-1167.2011.02989.x. Epub 2011 Mar 2. Epilepsia. 2011. PMID: 21366555 Free article.

6

Tackling Epilepsy With High-definition Precision Medicine: A Review.

Kearney H, Byrne S, Cavalleri GL, Delanty N. Kearney H, et al. Among authors: byrne s. JAMA Neurol. 2019 Sep 1;76(9):1109-1116. doi: 10.1001/jamaneurol.2019.2384. JAMA Neurol. 2019. PMID: 31380988

7

A comparison of genomic diagnostics in adults and children with epilepsy and comorbid intellectual disability.

Benson KA, White M, Allen NM, Byrne S, Carton R, Comerford E, Costello D, Doherty C, Dunleavey B, El-Naggar H, Gangadharan N, Heavin S, Kearney H, Lench NJ, Lynch J, McCormack M, Regan MO, Podesta K, Power K, Rogers AS, Steward CA, Sweeney B, Webb D, Fitzsimons M, Greally M, Delanty N, Cavalleri GL. Benson KA, et al. Among authors: byrne s. Eur J Hum Genet. 2020 Aug;28(8):1066-1077. doi: 10.1038/s41431-020-0610-3. Epub 2020 Apr 1. Eur J Hum Genet. 2020. PMID: 32238909 Free PMC article.

8

Precision therapy in the genetic epilepsies of childhood.

Byrne S, Enright N, Delanty N. Byrne S, et al. Dev Med Child Neurol. 2021 Nov;63(11):1276-1282. doi: 10.1111/dmcn.14929. Epub 2021 Jun 4. Dev Med Child Neurol. 2021. PMID: 34089185 Free article. Review.

9

Rate of familial amyotrophic lateral sclerosis: a systematic review and meta-analysis.

Byrne S, Walsh C, Lynch C, Bede P, Elamin M, Kenna K, McLaughlin R, Hardiman O. Byrne S, et al. J Neurol Neurosurg Psychiatry. 2011 Jun;82(6):623-7. doi: 10.1136/jnnp.2010.224501. Epub 2010 Nov 3. J Neurol Neurosurg Psychiatry. 2011. PMID: 21047878 Review.

10

Aggregation of neurologic and neuropsychiatric disease in amyotrophic lateral sclerosis kindreds: a population-based case-control cohort study of familial and sporadic amyotrophic lateral sclerosis.

Byrne S, Heverin M, Elamin M, Bede P, Lynch C, Kenna K, MacLaughlin R, Walsh C, Al Chalabi A, Hardiman O. Byrne S, et al. Ann Neurol. 2013 Nov;74(5):699-708. doi: 10.1002/ana.23969. Epub 2013 Sep 10. Ann Neurol. 2013. PMID: 23836460

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