Buyse G - Search Results

1

PRRT2 mutations: exploring the phenotypical boundaries.

Djémié T, Weckhuysen S, Holmgren P, Hardies K, Van Dyck T, Hendrickx R, Schoonjans AS, Van Paesschen W, Jansen AC, De Meirleir L, Selim LA, Girgis MY, Buyse G, Lagae L, Smets K, Smouts I, Claeys KG, Van den Bergh V, Grisar T, Blatt I, Shorer Z, Roelens F, Afawi Z, Helbig I, Ceulemans B, De Jonghe P, Suls A. Djémié T, et al. Among authors: buyse g. J Neurol Neurosurg Psychiatry. 2014 Apr;85(4):462-5. doi: 10.1136/jnnp-2013-305122. Epub 2013 Oct 7. J Neurol Neurosurg Psychiatry. 2014. PMID: 24101679

2

Microdeletions involving the SCN1A gene may be common in SCN1A-mutation-negative SMEI patients.

Suls A, Claeys KG, Goossens D, Harding B, Van Luijk R, Scheers S, Deprez L, Audenaert D, Van Dyck T, Beeckmans S, Smouts I, Ceulemans B, Lagae L, Buyse G, Barisic N, Misson JP, Wauters J, Del-Favero J, De Jonghe P, Claes LR. Suls A, et al. Among authors: buyse g. Hum Mutat. 2006 Sep;27(9):914-20. doi: 10.1002/humu.20350. Hum Mutat. 2006. PMID: 16865694

3

Novel mutations in the HSN2 gene causing hereditary sensory and autonomic neuropathy type II.

Coen K, Pareyson D, Auer-Grumbach M, Buyse G, Goemans N, Claeys KG, Verpoorten N, Laurà M, Scaioli V, Salmhofer W, Pieber TR, Nelis E, De Jonghe P, Timmerman V. Coen K, et al. Among authors: buyse g. Neurology. 2006 Mar 14;66(5):748-51. doi: 10.1212/01.wnl.0000201191.57519.47. Neurology. 2006. PMID: 16534117

4

Ring chromosome 20 syndrome: electroclinical description of six patients and review of the literature.

Elens I, Vanrykel K, De Waele L, Jansen K, Segeren M, Van Paesschen W, Ceulemans B, Boel M, Frijns JP, Buyse G, Lagae L. Elens I, et al. Among authors: buyse g. Epilepsy Behav. 2012 Apr;23(4):409-14. doi: 10.1016/j.yebeh.2012.02.008. Epub 2012 Mar 15. Epilepsy Behav. 2012. PMID: 22424860 Review.

5

Clinical experience with levetiracetam in childhood epilepsy: an add-on and mono-therapy trial.

Lagae L, Buyse G, Ceulemans B. Lagae L, et al. Among authors: buyse g. Seizure. 2005 Jan;14(1):66-71. doi: 10.1016/j.seizure.2004.10.004. Seizure. 2005. PMID: 15642504 Free article.

6

Gain-of-function FHF1 mutation causes early-onset epileptic encephalopathy with cerebellar atrophy.

Siekierska A, Isrie M, Liu Y, Scheldeman C, Vanthillo N, Lagae L, de Witte PA, Van Esch H, Goldfarb M, Buyse GM. Siekierska A, et al. Neurology. 2016 Jun 7;86(23):2162-70. doi: 10.1212/WNL.0000000000002752. Epub 2016 May 4. Neurology. 2016. PMID: 27164707 Free PMC article.

7

Investigating the genetic basis of fever-associated syndromic epilepsies using copy number variation analysis.

Hartmann C, von Spiczak S, Suls A, Weckhuysen S, Buyse G, Vilain C, Van Bogaert P, De Jonghe P, Cook J, Muhle H, Stephani U, Helbig I, Mefford HC. Hartmann C, et al. Among authors: buyse g. Epilepsia. 2015 Mar;56(3):e26-32. doi: 10.1111/epi.12920. Epub 2015 Feb 17. Epilepsia. 2015. PMID: 25690317 Free PMC article.

8

Effect of levetiracetam in refractory childhood epilepsy syndromes.

Lagae L, Buyse G, Deconinck A, Ceulemans B. Lagae L, et al. Among authors: buyse g. Eur J Paediatr Neurol. 2003;7(3):123-8. doi: 10.1016/s1090-3798(03)00041-2. Eur J Paediatr Neurol. 2003. PMID: 12788038

9

Steroids in intractable childhood epilepsy: clinical experience and review of the literature.

Verhelst H, Boon P, Buyse G, Ceulemans B, D'Hooghe M, Meirleir LD, Hasaerts D, Jansen A, Lagae L, Meurs A, Coster RV, Vonck K. Verhelst H, et al. Among authors: buyse g. Seizure. 2005 Sep;14(6):412-21. doi: 10.1016/j.seizure.2005.07.002. Seizure. 2005. PMID: 16087358 Free article.

10

Anti-epileptogenesis research: the clinical relevance.

Lagae L, Buyse G, Ceulemans B, Claeys P, Dedeurwaerdere S, de Meirleir L, Hauman R, Janssen A, Schmedding E, Verhelst H, Vonck K. Lagae L, et al. Among authors: buyse g. Acta Neurol Belg. 2003 Jun;103(2):78-82. Acta Neurol Belg. 2003. PMID: 12892000 Review.

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