An-Gourfinkel I - Search Results

1

Understanding Lennox-Gastaut syndrome: insights from focal epilepsy patients with Lennox-Gastaut features.

Dupont S, Banica-Wolters R, An-Gourfinkel I, Lambrecq V, Navarro V, Adam C, Nguyen-Michel VH. Dupont S, et al. Among authors: an gourfinkel i. J Neurol. 2017 Jul;264(7):1388-1396. doi: 10.1007/s00415-017-8535-7. Epub 2017 Jun 5. J Neurol. 2017. PMID: 28584915

2

K-complex-induced seizures in autosomal dominant nocturnal frontal lobe epilepsy.

El Helou J, Navarro V, Depienne C, Fedirko E, LeGuern E, Baulac M, An-Gourfinkel I, Adam C. El Helou J, et al. Among authors: an gourfinkel i. Clin Neurophysiol. 2008 Oct;119(10):2201-4. doi: 10.1016/j.clinph.2008.07.212. Epub 2008 Aug 31. Clin Neurophysiol. 2008. PMID: 18762450

3

DEPDC5 mutations in families presenting as autosomal dominant nocturnal frontal lobe epilepsy.

Picard F, Makrythanasis P, Navarro V, Ishida S, de Bellescize J, Ville D, Weckhuysen S, Fosselle E, Suls A, De Jonghe P, Vasselon Raina M, Lesca G, Depienne C, An-Gourfinkel I, Vlaicu M, Baulac M, Mundwiller E, Couarch P, Combi R, Ferini-Strambi L, Gambardella A, Antonarakis SE, Leguern E, Steinlein O, Baulac S. Picard F, et al. Among authors: an gourfinkel i. Neurology. 2014 Jun 10;82(23):2101-6. doi: 10.1212/WNL.0000000000000488. Epub 2014 May 9. Neurology. 2014. PMID: 24814846

4

Novel GABRG2 mutations cause familial febrile seizures.

Boillot M, Morin-Brureau M, Picard F, Weckhuysen S, Lambrecq V, Minetti C, Striano P, Zara F, Iacomino M, Ishida S, An-Gourfinkel I, Daniau M, Hardies K, Baulac M, Dulac O, Leguern E, Nabbout R, Baulac S. Boillot M, et al. Among authors: an gourfinkel i. Neurol Genet. 2015 Nov 4;1(4):e35. doi: 10.1212/NXG.0000000000000035. eCollection 2015 Dec. Neurol Genet. 2015. PMID: 27066572 Free PMC article.

5

Involvement of GATOR complex genes in familial focal epilepsies and focal cortical dysplasia.

Weckhuysen S, Marsan E, Lambrecq V, Marchal C, Morin-Brureau M, An-Gourfinkel I, Baulac M, Fohlen M, Kallay Zetchi C, Seeck M, de la Grange P, Dermaut B, Meurs A, Thomas P, Chassoux F, Leguern E, Picard F, Baulac S. Weckhuysen S, et al. Among authors: an gourfinkel i. Epilepsia. 2016 Jun;57(6):994-1003. doi: 10.1111/epi.13391. Epub 2016 May 13. Epilepsia. 2016. PMID: 27173016 Free article.

6

Absence of linkage to 8q24 in a European family with familial adult myoclonic epilepsy (FAME).

Labauge P, Amer LO, Simonetta-Moreau M, Attané F, Tannier C, Clanet M, Castelnovo G, An-Gourfinkel I, Agid Y, Brice A, Ducros A, LeGuern E. Labauge P, et al. Neurology. 2002 Mar 26;58(6):941-4. doi: 10.1212/wnl.58.6.941. Neurology. 2002. PMID: 11914412

7

Focal epilepsy as the revealing symptom of 5,10-methylenetetrahydrofolate reductase deficiency in a young adult.

Mezouar N, Mochel F, An-Gourfinkel I, Baulac M, Gales A. Mezouar N, et al. Among authors: an gourfinkel i. Rev Neurol (Paris). 2018 Mar;174(3):173-175. doi: 10.1016/j.neurol.2017.06.028. Epub 2018 Feb 1. Rev Neurol (Paris). 2018. PMID: 29366491 No abstract available.

8

Multidisciplinary approach of organic catatonia in children and adolescents may improve treatment decision making.

Lahutte B, Cornic F, Bonnot O, Consoli A, An-Gourfinkel I, Amoura Z, Sedel F, Cohen D. Lahutte B, et al. Among authors: an gourfinkel i. Prog Neuropsychopharmacol Biol Psychiatry. 2008 Aug 1;32(6):1393-8. doi: 10.1016/j.pnpbp.2008.02.015. Epub 2008 Mar 7. Prog Neuropsychopharmacol Biol Psychiatry. 2008. PMID: 18417262 Review.

9

Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2.

Escayg A, MacDonald BT, Meisler MH, Baulac S, Huberfeld G, An-Gourfinkel I, Brice A, LeGuern E, Moulard B, Chaigne D, Buresi C, Malafosse A. Escayg A, et al. Nat Genet. 2000 Apr;24(4):343-5. doi: 10.1038/74159. Nat Genet. 2000. PMID: 10742094 No abstract available.

10

Heterogeneous intracellular localization and expression of ataxin-3.

Trottier Y, Cancel G, An-Gourfinkel I, Lutz Y, Weber C, Brice A, Hirsch E, Mandel JL. Trottier Y, et al. Neurobiol Dis. 1998 Nov;5(5):335-47. doi: 10.1006/nbdi.1998.0208. Neurobiol Dis. 1998. PMID: 10069576

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