Wagnon JL - Search Results

1

Recurrent and Non-Recurrent Mutations of SCN8A in Epileptic Encephalopathy.

Wagnon JL, Meisler MH. Wagnon JL, et al. Front Neurol. 2015 May 15;6:104. doi: 10.3389/fneur.2015.00104. eCollection 2015. Front Neurol. 2015. PMID: 26029160 Free PMC article. Review.

2

Convulsive seizures and SUDEP in a mouse model of SCN8A epileptic encephalopathy.

Wagnon JL, Korn MJ, Parent R, Tarpey TA, Jones JM, Hammer MF, Murphy GG, Parent JM, Meisler MH. Wagnon JL, et al. Hum Mol Genet. 2015 Jan 15;24(2):506-15. doi: 10.1093/hmg/ddu470. Epub 2014 Sep 16. Hum Mol Genet. 2015. PMID: 25227913 Free PMC article.

3

Pathogenic mechanism of recurrent mutations of SCN8A in epileptic encephalopathy.

Wagnon JL, Barker BS, Hounshell JA, Haaxma CA, Shealy A, Moss T, Parikh S, Messer RD, Patel MK, Meisler MH. Wagnon JL, et al. Ann Clin Transl Neurol. 2015 Dec 21;3(2):114-23. doi: 10.1002/acn3.276. eCollection 2016 Feb. Ann Clin Transl Neurol. 2015. PMID: 26900580 Free PMC article.

4

SCN8A encephalopathy: Research progress and prospects.

Meisler MH, Helman G, Hammer MF, Fureman BE, Gaillard WD, Goldin AL, Hirose S, Ishii A, Kroner BL, Lossin C, Mefford HC, Parent JM, Patel M, Schreiber J, Stewart R, Whittemore V, Wilcox K, Wagnon JL, Pearl PL, Vanderver A, Scheffer IE. Meisler MH, et al. Among authors: wagnon jl. Epilepsia. 2016 Jul;57(7):1027-35. doi: 10.1111/epi.13422. Epub 2016 Jun 8. Epilepsia. 2016. PMID: 27270488 Free PMC article.

5

The SCN8A encephalopathy mutation p.Ile1327Val displays elevated sensitivity to the anticonvulsant phenytoin.

Barker BS, Ottolini M, Wagnon JL, Hollander RM, Meisler MH, Patel MK. Barker BS, et al. Among authors: wagnon jl. Epilepsia. 2016 Sep;57(9):1458-66. doi: 10.1111/epi.13461. Epub 2016 Jul 4. Epilepsia. 2016. PMID: 27375106 Free PMC article.

6

Cardiac arrhythmia in a mouse model of sodium channel SCN8A epileptic encephalopathy.

Frasier CR, Wagnon JL, Bao YO, McVeigh LG, Lopez-Santiago LF, Meisler MH, Isom LL. Frasier CR, et al. Among authors: wagnon jl. Proc Natl Acad Sci U S A. 2016 Nov 8;113(45):12838-12843. doi: 10.1073/pnas.1612746113. Epub 2016 Oct 26. Proc Natl Acad Sci U S A. 2016. PMID: 27791149 Free PMC article.

7

Altered gene expression profile in a mouse model of SCN8A encephalopathy.

Sprissler RS, Wagnon JL, Bunton-Stasyshyn RK, Meisler MH, Hammer MF. Sprissler RS, et al. Among authors: wagnon jl. Exp Neurol. 2017 Feb;288:134-141. doi: 10.1016/j.expneurol.2016.11.002. Epub 2016 Nov 9. Exp Neurol. 2017. PMID: 27836728 Free PMC article.

8

Neuronal hyperexcitability in a mouse model of SCN8A epileptic encephalopathy.

Lopez-Santiago LF, Yuan Y, Wagnon JL, Hull JM, Frasier CR, O'Malley HA, Meisler MH, Isom LL. Lopez-Santiago LF, et al. Among authors: wagnon jl. Proc Natl Acad Sci U S A. 2017 Feb 28;114(9):2383-2388. doi: 10.1073/pnas.1616821114. Epub 2017 Feb 13. Proc Natl Acad Sci U S A. 2017. PMID: 28193882 Free PMC article.

9

Loss-of-function variants of SCN8A in intellectual disability without seizures.

Wagnon JL, Barker BS, Ottolini M, Park Y, Volkheimer A, Valdez P, Swinkels MEM, Patel MK, Meisler MH. Wagnon JL, et al. Neurol Genet. 2017 Jun 7;3(4):e170. doi: 10.1212/NXG.0000000000000170. eCollection 2017 Aug. Neurol Genet. 2017. PMID: 28702509 Free PMC article.

10

Partial loss-of-function of sodium channel SCN8A in familial isolated myoclonus.

Wagnon JL, Mencacci NE, Barker BS, Wengert ER, Bhatia KP, Balint B, Carecchio M, Wood NW, Patel MK, Meisler MH. Wagnon JL, et al. Hum Mutat. 2018 Jul;39(7):965-969. doi: 10.1002/humu.23547. Epub 2018 May 17. Hum Mutat. 2018. PMID: 29726066 Free PMC article.

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