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Clinical and genetic aspects of PCDH19-related epilepsy syndromes and the possible role of PCDH19 mutations in males with autism spectrum disorders.
van Harssel JJ, Weckhuysen S, van Kempen MJ, Hardies K, Verbeek NE, de Kovel CG, Gunning WB, van Daalen E, de Jonge MV, Jansen AC, Vermeulen RJ, Arts WF, Verhelst H, Fogarasi A, de Rijk-van Andel JF, Kelemen A, Lindhout D, De Jonghe P, Koeleman BP, Suls A, Brilstra EH. van Harssel JJ, et al. Among authors: gunning wb. Neurogenetics. 2013 Feb;14(1):23-34. doi: 10.1007/s10048-013-0353-1. Epub 2013 Jan 20. Neurogenetics. 2013. PMID: 23334464
Effect of vaccinations on seizure risk and disease course in Dravet syndrome.
Verbeek NE, van der Maas NA, Sonsma AC, Ippel E, Vermeer-de Bondt PE, Hagebeuk E, Jansen FE, Geesink HH, Braun KP, de Louw A, Augustijn PB, Neuteboom RF, Schieving JH, Stroink H, Vermeulen RJ, Nicolai J, Brouwer OF, van Kempen M, de Kovel CG, Kemmeren JM, Koeleman BP, Knoers NV, Lindhout D, Gunning WB, Brilstra EH. Verbeek NE, et al. Among authors: gunning wb. Neurology. 2015 Aug 18;85(7):596-603. doi: 10.1212/WNL.0000000000001855. Epub 2015 Jul 22. Neurology. 2015. PMID: 26203087
Photosensitivity in Dravet syndrome is under-recognized and related to prognosis.
Verbeek N, Kasteleijn-Nolst Trenité D, Wassenaar M, van Campen J, Sonsma A, Gunning WB, de Weerd A, Knoers N, Spetgens W, Gutter T, Leijten F, Brilstra E. Verbeek N, et al. Among authors: gunning wb. Clin Neurophysiol. 2017 Feb;128(2):323-330. doi: 10.1016/j.clinph.2016.11.021. Epub 2016 Dec 6. Clin Neurophysiol. 2017. PMID: 28042998
Cardiac arrhythmias in Dravet syndrome: an observational multicenter study.
Shmuely S, Surges R, Helling RM, Gunning WB, Brilstra EH, Verhoeven JS, Cross JH, Sisodiya SM, Tan HL, Sander JW, Thijs RD. Shmuely S, et al. Among authors: gunning wb. Ann Clin Transl Neurol. 2020 Apr;7(4):462-473. doi: 10.1002/acn3.51017. Epub 2020 Mar 24. Ann Clin Transl Neurol. 2020. PMID: 32207228 Free PMC article.
Mortality in Dravet syndrome: A review.
Shmuely S, Sisodiya SM, Gunning WB, Sander JW, Thijs RD. Shmuely S, et al. Among authors: gunning wb. Epilepsy Behav. 2016 Nov;64(Pt A):69-74. doi: 10.1016/j.yebeh.2016.09.007. Epub 2016 Oct 11. Epilepsy Behav. 2016. PMID: 27732919 Free article. Review.
A whole-genome scan in 164 Dutch sib pairs with attention-deficit/hyperactivity disorder: suggestive evidence for linkage on chromosomes 7p and 15q.
Bakker SC, van der Meulen EM, Buitelaar JK, Sandkuijl LA, Pauls DL, Monsuur AJ, van 't Slot R, Minderaa RB, Gunning WB, Pearson PL, Sinke RJ. Bakker SC, et al. Among authors: gunning wb. Am J Hum Genet. 2003 May;72(5):1251-60. doi: 10.1086/375143. Epub 2003 Apr 4. Am J Hum Genet. 2003. PMID: 12679898 Free PMC article.
38 results