Ceulemans B - Search Results

1

Aberrant Inclusion of a Poison Exon Causes Dravet Syndrome and Related SCN1A-Associated Genetic Epilepsies.

Carvill GL, Engel KL, Ramamurthy A, Cochran JN, Roovers J, Stamberger H, Lim N, Schneider AL, Hollingsworth G, Holder DH, Regan BM, Lawlor J, Lagae L, Ceulemans B, Bebin EM, Nguyen J; EuroEPINOMICS Rare Epilepsy Syndrome, Myoclonic-Astatic Epilepsy, and Dravet Working Group; Barsh GS, Weckhuysen S, Meisler M, Berkovic SF, De Jonghe P, Scheffer IE, Myers RM, Cooper GM, Mefford HC. Carvill GL, et al. Among authors: ceulemans b. Am J Hum Genet. 2018 Dec 6;103(6):1022-1029. doi: 10.1016/j.ajhg.2018.10.023. Am J Hum Genet. 2018. PMID: 30526861 Free PMC article.

2

The X-linked infantile spasms syndrome (MIM 308350) maps to Xp11.4-Xpter in two pedigrees.

Claes S, Devriendt K, Lagae L, Ceulemans B, Dom L, Casaer P, Raeymaekers P, Cassiman JJ, Fryns JP. Claes S, et al. Among authors: ceulemans b. Ann Neurol. 1997 Sep;42(3):360-4. doi: 10.1002/ana.410420313. Ann Neurol. 1997. PMID: 9307258

3

De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy.

Claes L, Del-Favero J, Ceulemans B, Lagae L, Van Broeckhoven C, De Jonghe P. Claes L, et al. Among authors: ceulemans b. Am J Hum Genet. 2001 Jun;68(6):1327-32. doi: 10.1086/320609. Epub 2001 May 15. Am J Hum Genet. 2001. PMID: 11359211 Free PMC article.

4

De novo SCN1A mutations are a major cause of severe myoclonic epilepsy of infancy.

Claes L, Ceulemans B, Audenaert D, Smets K, Löfgren A, Del-Favero J, Ala-Mello S, Basel-Vanagaite L, Plecko B, Raskin S, Thiry P, Wolf NI, Van Broeckhoven C, De Jonghe P. Claes L, et al. Among authors: ceulemans b. Hum Mutat. 2003 Jun;21(6):615-21. doi: 10.1002/humu.10217. Hum Mutat. 2003. PMID: 12754708

5

Effect of levetiracetam in refractory childhood epilepsy syndromes.

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

6

A deletion in SCN1B is associated with febrile seizures and early-onset absence epilepsy.

Audenaert D, Claes L, Ceulemans B, Löfgren A, Van Broeckhoven C, De Jonghe P. Audenaert D, et al. Among authors: ceulemans b. Neurology. 2003 Sep 23;61(6):854-6. doi: 10.1212/01.wnl.0000080362.55784.1c. Neurology. 2003. PMID: 14504340

7

Clinical correlations of mutations in the SCN1A gene: from febrile seizures to severe myoclonic epilepsy in infancy.

Ceulemans BP, Claes LR, Lagae LG. Ceulemans BP, et al. Pediatr Neurol. 2004 Apr;30(4):236-43. doi: 10.1016/j.pediatrneurol.2003.10.012. Pediatr Neurol. 2004. PMID: 15087100

8

Severe myoclonic epilepsy in infancy: toward an optimal treatment.

Ceulemans B, Boel M, Claes L, Dom L, Willekens H, Thiry P, Lagae L. Ceulemans B, et al. J Child Neurol. 2004 Jul;19(7):516-21. doi: 10.1177/08830738040190070701. J Child Neurol. 2004. PMID: 15526956

9

De novo KCNQ2 mutations in patients with benign neonatal seizures.

Claes LR, Ceulemans B, Audenaert D, Deprez L, Jansen A, Hasaerts D, Weckx S, Claeys KG, Del-Favero J, Van Broeckhoven C, De Jonghe P. Claes LR, et al. Among authors: ceulemans b. Neurology. 2004 Dec 14;63(11):2155-8. doi: 10.1212/01.wnl.0000145629.94338.89. Neurology. 2004. PMID: 15596769

10

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: ceulemans b. Seizure. 2005 Jan;14(1):66-71. doi: 10.1016/j.seizure.2004.10.004. Seizure. 2005. PMID: 15642504 Free article.

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