Bye AM - Search Results

1

Hope in the uncertainties and certainty for parents of children with rare neurological disorders: Part 2 (of 3): Certainty.

Nevin SM, Beavis E, Macintosh R, Palmer EE, Sachdev R, Le Marne FA, Bye AM, Nunn K. Nevin SM, et al. Among authors: bye am. J Paediatr Child Health. 2022 Oct;58(10):1722-1725. doi: 10.1111/jpc.16202. Epub 2022 Sep 7. J Paediatr Child Health. 2022. PMID: 36069627

2

Personalised epilepsy education intervention for adolescents and impact on knowledge acquisition and psychosocial function.

Frizzell CK, Connolly AM, Beavis E, Lawson JA, Bye AM. Frizzell CK, et al. Among authors: bye am. J Paediatr Child Health. 2011 May;47(5):271-5. doi: 10.1111/j.1440-1754.2010.01952.x. Epub 2011 Jan 18. J Paediatr Child Health. 2011. PMID: 21244556

3

'Beyond Milestones': a randomised controlled trial evaluating an innovative digital resource teaching quality observation of normal child development.

Connolly AM, Cunningham C, Sinclair AJ, Rao A, Lonergan A, Bye AM. Connolly AM, et al. Among authors: bye am. J Paediatr Child Health. 2014 May;50(5):393-8. doi: 10.1111/jpc.12485. Epub 2013 Dec 23. J Paediatr Child Health. 2014. PMID: 24373114 Clinical Trial.

4

Exploring carer perceptions of training in out-of-hospital use of buccal midazolam for emergency management of seizures (2008-2012).

Connolly AM, Beavis E, Mugica-Cox B, Bye AM, Lawson JA. Connolly AM, et al. Among authors: bye am. J Paediatr Child Health. 2015 Jul;51(7):704-7. doi: 10.1111/jpc.12811. Epub 2015 Jan 15. J Paediatr Child Health. 2015. PMID: 25594133

5

Asparagine Synthetase Deficiency causes reduced proliferation of cells under conditions of limited asparagine.

Palmer EE, Hayner J, Sachdev R, Cardamone M, Kandula T, Morris P, Dias KR, Tao J, Miller D, Zhu Y, Macintosh R, Dinger ME, Cowley MJ, Buckley MF, Roscioli T, Bye A, Kilberg MS, Kirk EP. Palmer EE, et al. Mol Genet Metab. 2015 Nov;116(3):178-86. doi: 10.1016/j.ymgme.2015.08.007. Epub 2015 Aug 14. Mol Genet Metab. 2015. PMID: 26318253 Free PMC article.

6

Neuronal deficiency of ARV1 causes an autosomal recessive epileptic encephalopathy.

Palmer EE, Jarrett KE, Sachdev RK, Al Zahrani F, Hashem MO, Ibrahim N, Sampaio H, Kandula T, Macintosh R, Gupta R, Conlon DM, Billheimer JT, Rader DJ, Funato K, Walkey CJ, Lee CS, Loo C, Brammah S, Elakis G, Zhu Y, Buckley M, Kirk EP, Bye A, Alkuraya FS, Roscioli T, Lagor WR. Palmer EE, et al. Hum Mol Genet. 2016 Jul 15;25(14):3042-3054. doi: 10.1093/hmg/ddw157. Epub 2016 Jun 6. Hum Mol Genet. 2016. PMID: 27270415 Free PMC article.

7

Evaluation of an E-learning resource on approach to the first unprovoked seizure.

Le Marne FA, McGinness H, Slade R, Cardamone M, Balbir Singh S, Connolly AM, Bye AM. Le Marne FA, et al. Among authors: bye am. J Paediatr Child Health. 2016 Sep;52(9):896-900. doi: 10.1111/jpc.13277. J Paediatr Child Health. 2016. PMID: 27650145

8

Unusual case of tuberculous meningitis with discordant ventricular and lumbar cerebrospinal fluid; lessons in the era of world-wide migration.

Said M, Uppal P, Bye A, Palasanthiran P. Said M, et al. J Paediatr Child Health. 2018 Jan;54(1):93-95. doi: 10.1111/jpc.13665. Epub 2017 Aug 14. J Paediatr Child Health. 2018. PMID: 28805285 No abstract available.

9

A De Novo Mutation in the Sodium-Activated Potassium Channel KCNT2 Alters Ion Selectivity and Causes Epileptic Encephalopathy.

Gururaj S, Palmer EE, Sheehan GD, Kandula T, Macintosh R, Ying K, Morris P, Tao J, Dias KR, Zhu Y, Dinger ME, Cowley MJ, Kirk EP, Roscioli T, Sachdev R, Duffey ME, Bye A, Bhattacharjee A. Gururaj S, et al. Cell Rep. 2017 Oct 24;21(4):926-933. doi: 10.1016/j.celrep.2017.09.088. Cell Rep. 2017. PMID: 29069600 Free PMC article.

10

Integrating exome sequencing into a diagnostic pathway for epileptic encephalopathy: Evidence of clinical utility and cost effectiveness.

Palmer EE, Schofield D, Shrestha R, Kandula T, Macintosh R, Lawson JA, Andrews I, Sampaio H, Johnson AM, Farrar MA, Cardamone M, Mowat D, Elakis G, Lo W, Zhu Y, Ying K, Morris P, Tao J, Dias KR, Buckley M, Dinger ME, Cowley MJ, Roscioli T, Kirk EP, Bye A, Sachdev RK. Palmer EE, et al. Among authors: bye a. Mol Genet Genomic Med. 2018 Mar;6(2):186-199. doi: 10.1002/mgg3.355. Epub 2018 Jan 4. Mol Genet Genomic Med. 2018. PMID: 29314763 Free PMC article.

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