Lagae L - Search Results

1

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: lagae l. 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.

2

A novel GABRG2 mutation associated with febrile seizures.

Audenaert D, Schwartz E, Claeys KG, Claes L, Deprez L, Suls A, Van Dyck T, Lagae L, Van Broeckhoven C, Macdonald RL, De Jonghe P. Audenaert D, et al. Among authors: lagae l. Neurology. 2006 Aug 22;67(4):687-90. doi: 10.1212/01.wnl.0000230145.73496.a2. Neurology. 2006. PMID: 16924025 Clinical Trial.

3

Clinical spectrum of early-onset epileptic encephalopathies associated with STXBP1 mutations.

Deprez L, Weckhuysen S, Holmgren P, Suls A, Van Dyck T, Goossens D, Del-Favero J, Jansen A, Verhaert K, Lagae L, Jordanova A, Van Coster R, Yendle S, Berkovic SF, Scheffer I, Ceulemans B, De Jonghe P. Deprez L, et al. Among authors: lagae l. Neurology. 2010 Sep 28;75(13):1159-65. doi: 10.1212/WNL.0b013e3181f4d7bf. Neurology. 2010. PMID: 20876469

4

Effect of levetiracetam in refractory childhood epilepsy syndromes.

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

5

Low-dose fenfluramine significantly reduces seizure frequency in Dravet syndrome: a prospective study of a new cohort of patients.

Schoonjans A, Paelinck BP, Marchau F, Gunning B, Gammaitoni A, Galer BS, Lagae L, Ceulemans B. Schoonjans A, et al. Among authors: lagae l. Eur J Neurol. 2017 Feb;24(2):309-314. doi: 10.1111/ene.13195. Epub 2016 Oct 28. Eur J Neurol. 2017. PMID: 27790834 Free PMC article.

6

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

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

7

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: lagae l. Ann Neurol. 1997 Sep;42(3):360-4. doi: 10.1002/ana.410420313. Ann Neurol. 1997. PMID: 9307258

8

Classical Ehlers-Danlos syndrome caused by a mutation in type I collagen.

Nuytinck L, Freund M, Lagae L, Pierard GE, Hermanns-Le T, De Paepe A. Nuytinck L, et al. Among authors: lagae l. Am J Hum Genet. 2000 Apr;66(4):1398-402. doi: 10.1086/302859. Epub 2000 Mar 17. Am J Hum Genet. 2000. PMID: 10739762 Free PMC article.

9

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. Acta Neurol Belg. 2003 Jun;103(2):78-82. Acta Neurol Belg. 2003. PMID: 12892000 Review.

10

Refractory photosensitive epilepsy associated with a complex rearrangement of chromosome 2.

Van Esch H, Syrrou M, Lagae L. Van Esch H, et al. Among authors: lagae l. Neuropediatrics. 2002 Dec;33(6):320-3. doi: 10.1055/s-2002-37088. Neuropediatrics. 2002. PMID: 12571788

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

399 results

Search Page