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Items: 1 to 50 of 203

1.

Treatment of Juvenile Myoclonic Epilepsy in Patients of Child-Bearing Potential.

Serafini A, Gerard E, Genton P, Crespel A, Gelisse P.

CNS Drugs. 2019 Mar;33(3):195-208. doi: 10.1007/s40263-018-00602-2.

PMID:
30747367
2.

Perampanel in 12 patients with Unverricht-Lundborg disease.

Crespel A, Gelisse P, Tang NP, Genton P.

Epilepsia. 2017 Apr;58(4):543-547. doi: 10.1111/epi.13662. Epub 2017 Feb 6.

3.

The 'Photosensitivity Model' is (also) a model for focal (partial) seizures.

Kasteleijn-Nolst Trenite D, Genton P, Brandt C, Reed RC.

Epilepsy Res. 2017 Jul;133:113-120. doi: 10.1016/j.eplepsyres.2016.11.012. Epub 2016 Dec 2. Review.

PMID:
28034485
4.

Lafora disease.

Turnbull J, Tiberia E, Striano P, Genton P, Carpenter S, Ackerley CA, Minassian BA.

Epileptic Disord. 2016 Sep 1;18(S2):38-62. Review.

5.

Myoclonus and seizures in progressive myoclonus epilepsies: pharmacology and therapeutic trials.

Michelucci R, Pasini E, Riguzzi P, Andermann E, Kälviäinen R, Genton P.

Epileptic Disord. 2016 Sep 1;18(S2):145-153. Review.

PMID:
27629998
6.

The history of progressive myoclonus epilepsies.

Genton P, Striano P, Minassian BA.

Epileptic Disord. 2016 Sep 1;18(S2):3-10. Review.

7.

Autosomal recessive progressive myoclonus epilepsy due to impaired ceramide synthesis.

Ferlazzo E, Striano P, Italiano D, Calarese T, Gasparini S, Vanni N, Fruscione F, Genton P, Zara F.

Epileptic Disord. 2016 Sep 1;18(S2):120-127.

PMID:
27618929
8.

Unverricht-Lundborg disease.

Crespel A, Ferlazzo E, Franceschetti S, Genton P, Gouider R, Kälviäinen R, Korja M, Lehtinen MK, Mervaala E, Simonato M, Vaarmann A.

Epileptic Disord. 2016 Sep 1;18(S2):28-37. Review.

PMID:
27582036
9.

Is there a difference between various presentations of valproate for cognitive outcome after in utero exposure?

Gelisse P, Genton P, Crespel A.

Epilepsia. 2016 Mar;57(3):523-4. doi: 10.1111/epi.13301. No abstract available.

10.

Brivaracetam in Unverricht-Lundborg disease (EPM1): Results from two randomized, double-blind, placebo-controlled studies.

Kälviäinen R, Genton P, Andermann E, Andermann F, Magaudda A, Frucht SJ, Schlit AF, Gerard D, de la Loge C, von Rosenstiel P.

Epilepsia. 2016 Feb;57(2):210-21. doi: 10.1111/epi.13275. Epub 2015 Dec 15.

11.

Can emotional stress trigger the onset of epilepsy?

Gélisse P, Genton P, Coubes P, Tang NP, Crespel A.

Epilepsy Behav. 2015 Jul;48:15-20. doi: 10.1016/j.yebeh.2015.05.010. Epub 2015 May 28.

PMID:
26037844
12.

Novel carboxypeptidase A6 (CPA6) mutations identified in patients with juvenile myoclonic and generalized epilepsy.

Sapio MR, Vessaz M, Thomas P, Genton P, Fricker LD, Salzmann A.

PLoS One. 2015 Apr 13;10(4):e0123180. doi: 10.1371/journal.pone.0123180. eCollection 2015.

13.

Are c.436G>A mutations less severe forms of Lafora disease? A case report.

Lanoiselée HM, Genton P, Lesca G, Brault F, De Toffol B.

Epilepsy Behav Case Rep. 2014 Jan 19;2:19-21. doi: 10.1016/j.ebcr.2013.11.003. eCollection 2014.

14.

Transition for patients with epilepsy due to metabolic and mitochondrial disorders.

Kossoff EH, Veggiotti P, Genton P, Desguerre I.

Epilepsia. 2014 Aug;55 Suppl 3:37-40. doi: 10.1111/epi.12709. Review.

15.

Joseph Roger. 1918-2012.

Dravet C, Bureau M, Soulayrol R, Genton P.

Neurophysiol Clin. 2014 Apr;44(2):151-2. No abstract available.

PMID:
25065023
16.

Zonisamide for refractory juvenile absence epilepsy.

Velizarova R, Crespel A, Genton P, Serafini A, Gelisse P.

Epilepsy Res. 2014 Sep;108(7):1263-6. doi: 10.1016/j.eplepsyres.2014.04.010. Epub 2014 May 14.

PMID:
24907183
17.

Impairment of ceramide synthesis causes a novel progressive myoclonus epilepsy.

Vanni N, Fruscione F, Ferlazzo E, Striano P, Robbiano A, Traverso M, Sander T, Falace A, Gazzerro E, Bramanti P, Bielawski J, Fassio A, Minetti C, Genton P, Zara F.

Ann Neurol. 2014 Aug;76(2):206-12. doi: 10.1002/ana.24170. Epub 2014 May 20.

PMID:
24782409
18.

Consensus on diagnosis and management of JME: From founder's observations to current trends.

Kasteleijn-Nolst Trenité DG, Schmitz B, Janz D, Delgado-Escueta AV, Thomas P, Hirsch E, Lerche H, Camfield C, Baykan B, Feucht M, Martínez-Juárez IE, Duron RM, Medina MT, Rubboli G, Jerney J, Hermann B, Yacubian E, Koutroumanidis M, Stephani U, Salas-Puig J, Reed RC, Woermann F, Wandschneider B, Bureau M, Gambardella A, Koepp MJ, Gelisse P, Gurses C, Crespel A, Nguyen-Michel VH, Ferlazzo E, Grisar T, Helbig I, Koeleman BP, Striano P, Trimble M, Buono R, Cossette P, Represa A, Dravet C, Serafini A, Berglund IS, Sisodiya SM, Yamakawa K, Genton P.

Epilepsy Behav. 2013 Jul;28 Suppl 1:S87-90. doi: 10.1016/j.yebeh.2012.11.051.

PMID:
23756490
19.

Management of juvenile myoclonic epilepsy.

Crespel A, Gelisse P, Reed RC, Ferlazzo E, Jerney J, Schmitz B, Genton P.

Epilepsy Behav. 2013 Jul;28 Suppl 1:S81-6. doi: 10.1016/j.yebeh.2013.01.001. Review.

PMID:
23756489
20.

Clinical aspects of juvenile myoclonic epilepsy.

Genton P, Thomas P, Kasteleijn-Nolst Trenité DG, Medina MT, Salas-Puig J.

Epilepsy Behav. 2013 Jul;28 Suppl 1:S8-14. doi: 10.1016/j.yebeh.2012.10.034. Review.

PMID:
23756488
21.

The history of juvenile myoclonic epilepsy.

Genton P, Gelisse P.

Epilepsy Behav. 2013 Jul;28 Suppl 1:S2-7. doi: 10.1016/j.yebeh.2013.01.002. Review.

PMID:
23756475
22.

Juvenile myoclonic epilepsy.

Genton P, Kasteleijn-Nolst Trenite DG.

Epilepsy Behav. 2013 Jul;28 Suppl 1:S1. doi: 10.1016/j.yebeh.2012.11.038. No abstract available.

PMID:
23756472
23.

Efficacy of the histamine 3 receptor (H3R) antagonist pitolisant (formerly known as tiprolisant; BF2.649) in epilepsy: dose-dependent effects in the human photosensitivity model.

Kasteleijn-Nolst Trenité D, Parain D, Genton P, Masnou P, Schwartz JC, Hirsch E.

Epilepsy Behav. 2013 Jul;28(1):66-70. doi: 10.1016/j.yebeh.2013.03.018. Epub 2013 May 8.

PMID:
23665640
24.

Mutations of DEPDC5 cause autosomal dominant focal epilepsies.

Ishida S, Picard F, Rudolf G, Noé E, Achaz G, Thomas P, Genton P, Mundwiller E, Wolff M, Marescaux C, Miles R, Baulac M, Hirsch E, Leguern E, Baulac S.

Nat Genet. 2013 May;45(5):552-5. doi: 10.1038/ng.2601. Epub 2013 Mar 31.

25.

PRRT2 links infantile convulsions and paroxysmal dyskinesia with migraine.

Cloarec R, Bruneau N, Rudolf G, Massacrier A, Salmi M, Bataillard M, Boulay C, Caraballo R, Fejerman N, Genton P, Hirsch E, Hunter A, Lesca G, Motte J, Roubertie A, Sanlaville D, Wong SW, Fu YH, Rochette J, Ptácek LJ, Szepetowski P.

Neurology. 2012 Nov 20;79(21):2097-103. doi: 10.1212/WNL.0b013e3182752c46. Epub 2012 Oct 17.

26.

Results of an action-research on epilepsy in rural Mali.

Bruno E, Nimaga K, Foba I, Vignoles P, Genton P, Doumbo O, Gérard D, Preux PM, Farnarier G.

PLoS One. 2012;7(8):e44469. doi: 10.1371/journal.pone.0044469. Epub 2012 Aug 31.

27.

Epileptic encephalopathies of the Landau-Kleffner and continuous spike and waves during slow-wave sleep types: genomic dissection makes the link with autism.

Lesca G, Rudolf G, Labalme A, Hirsch E, Arzimanoglou A, Genton P, Motte J, de Saint Martin A, Valenti MP, Boulay C, De Bellescize J, Kéo-Kosal P, Boutry-Kryza N, Edery P, Sanlaville D, Szepetowski P.

Epilepsia. 2012 Sep;53(9):1526-38. doi: 10.1111/j.1528-1167.2012.03559.x. Epub 2012 Jun 27.

28.

Worsening of negative myoclonus by lamotrigine in a case of idiopathic focal epilepsy of children with long-term follow-up.

Gélisse P, Genton P, Velizarova R, Serafini A, Crespel A.

Brain Dev. 2012 Mar;34(3):248-50. doi: 10.1016/j.braindev.2011.05.001. Epub 2011 May 28.

PMID:
21621357
29.

Dravet syndrome: the long-term outcome.

Genton P, Velizarova R, Dravet C.

Epilepsia. 2011 Apr;52 Suppl 2:44-9. doi: 10.1111/j.1528-1167.2011.03001.x. Review.

30.

Valproate treatment after liver transplant in a patient with Lennox-Gastaut syndrome.

Velizarova R, Gelisse P, Pageaux GP, Genton P, Crespel A.

Seizure. 2011 Jul;20(6):500-1. doi: 10.1016/j.seizure.2011.02.005. Epub 2011 Mar 3.

31.

Unilateral continuous subclinical paroxysmal activity: an unusual finding in a patient with recurrent absence status.

Velizarova R, Genton P.

Epileptic Disord. 2010 Dec;12(4):316-20. doi: 10.1684/epd.2010.0342. Epub 2010 Nov 16.

32.

Pharmacoresistant occipital lobe epilepsy with fixation-off sensitivity in a patient with cerebral calcifications: a video/EEG study.

Ferlazzo E, Calarese T, Genton P.

Epilepsy Behav. 2010 Dec;19(4):647-9. doi: 10.1016/j.yebeh.2010.08.032. Epub 2010 Nov 3.

PMID:
21051297
33.

Temporal intermittent δ activity: a marker of juvenile absence epilepsy?

Gelisse P, Serafini A, Velizarova R, Genton P, Crespel A.

Seizure. 2011 Jan;20(1):38-41. doi: 10.1016/j.seizure.2010.10.003. Epub 2010 Nov 1.

34.

Does lacosamide aggravate Lennox-Gastaut syndrome? Report on three consecutive cases.

Cuzzola A, Ferlazzo E, Italiano D, Calabrò RS, Bramanti P, Genton P.

Epilepsy Behav. 2010 Dec;19(4):650-1. doi: 10.1016/j.yebeh.2010.09.024. Epub 2010 Oct 20.

PMID:
20970386
35.

Novel mutations in EPM2A and NHLRC1 widen the spectrum of Lafora disease.

Lesca G, Boutry-Kryza N, de Toffol B, Milh M, Steschenko D, Lemesle-Martin M, Maillard L, Foletti G, Rudolf G, Nielsen JE, á Rogvi-Hansen B, Erdal J, Mancini J, Thauvin-Robinet C, M'Rrabet A, Ville D, Szepetowski P, Raffo E, Hirsch E, Ryvlin P, Calender A, Genton P.

Epilepsia. 2010 Sep;51(9):1691-8. doi: 10.1111/j.1528-1167.2010.02692.x. Epub 2010 Aug 5.

36.

Senile myoclonic epilepsy: delineation of a common condition associated with Alzheimer's disease in Down syndrome.

De Simone R, Puig XS, Gélisse P, Crespel A, Genton P.

Seizure. 2010 Sep;19(7):383-9. doi: 10.1016/j.seizure.2010.04.008. Epub 2010 Jul 3.

37.

Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies.

Mefford HC, Muhle H, Ostertag P, von Spiczak S, Buysse K, Baker C, Franke A, Malafosse A, Genton P, Thomas P, Gurnett CA, Schreiber S, Bassuk AG, Guipponi M, Stephani U, Helbig I, Eichler EE.

PLoS Genet. 2010 May 20;6(5):e1000962. doi: 10.1371/journal.pgen.1000962.

38.

Unverricht-Lundborg disease (EPM1).

Genton P.

Epilepsia. 2010 Feb;51 Suppl 1:37-9. doi: 10.1111/j.1528-1167.2009.02441.x. No abstract available.

39.

Lennox-Gastaut syndrome in adulthood: clinical and EEG features.

Ferlazzo E, Nikanorova M, Italiano D, Bureau M, Dravet C, Calarese T, Viallat D, Kölmel M, Bramanti P, De Santi L, Genton P.

Epilepsy Res. 2010 May;89(2-3):271-7. doi: 10.1016/j.eplepsyres.2010.01.012. Epub 2010 Feb 10. Erratum in: Epilepsy Res. 2010 Aug;90(3):313. Nikaronova, Marina [corrected to Nikanorova, Marina].

PMID:
20149600
40.

Heterogeneous seizure manifestations in Hypomelanosis of Ito: report of four new cases and review of the literature.

Assogba K, Ferlazzo E, Striano P, Calarese T, Villeneuve N, Ivanov I, Bramanti P, Sessa E, Pacheva I, Genton P.

Neurol Sci. 2010 Feb;31(1):9-16. doi: 10.1007/s10072-009-0160-5. Epub 2009 Nov 10. Review.

PMID:
19902142
41.

T2-weighted high-intensity signals in the basal ganglia as an interesting image finding in Unverricht-Lundborg disease.

Korja M, Ferlazzo E, Soilu-Hänninen M, Magaudda A, Marttila R, Genton P, Parkkola R.

Epilepsy Res. 2010 Jan;88(1):87-91. doi: 10.1016/j.eplepsyres.2009.09.018. Epub 2009 Nov 6.

PMID:
19896804
42.

[Juvenile myoclonic epilepsy with recurrent myoclonic status: efficacy of valproate].

Crespel A, Velizarova R, Genton P, Gélisse P.

Therapie. 2009 Sep-Oct;64(5):321-3. doi: 10.2515/therapie/2009033. Epub 2009 Oct 30. French.

PMID:
19863907
43.

Wicket spikes misinterpreted as focal abnormalities in idiopathic generalized epilepsy with prescription of carbamazepine leading to paradoxical aggravation.

Crespel A, Velizarova R, Genton P, Coubes P, Gélisse P.

Neurophysiol Clin. 2009 Aug;39(3):139-42. doi: 10.1016/j.neucli.2009.02.004. Epub 2009 Mar 27.

PMID:
19716464
44.

Death in Unverricht-Lundborg disease.

Khiari HM, Franceschetti S, Jovic N, Mrabet A, Genton P.

Neurol Sci. 2009 Aug;30(4):315-8. doi: 10.1007/s10072-009-0102-2. Epub 2009 Jun 5.

PMID:
19499178
45.

[Epilepsy with absence status: A new syndrome of idiopathic generalized epilepsy].

Gélisse P, Velizarova R, Genton P, Crespel A.

Rev Neurol (Paris). 2009 Oct;165(10):839-41. doi: 10.1016/j.neurol.2009.03.009. Epub 2009 Apr 23. French. No abstract available.

PMID:
19394986
46.

Description of a family with a novel progressive myoclonus epilepsy and cognitive impairment.

Ferlazzo E, Italiano D, An I, Calarese T, Laguitton V, Bramanti P, Di Bella P, Genton P.

Mov Disord. 2009 May 15;24(7):1016-22. doi: 10.1002/mds.22489.

PMID:
19243074
47.

[Antiepileptic drugs].

Gélisse P, Crespel A, Genton P.

Therapie. 2008 Nov-Dec;63(6):425-51. doi: 10.2515/therapie/2008069. Epub 2009 Feb 24. Review. French.

PMID:
19236834
48.

Lennox-Gastaut syndrome with late-onset and prominent reflex seizures in trisomy 21 patients.

Ferlazzo E, Adjien CK, Guerrini R, Calarese T, Crespel A, Elia M, Striano P, Gelisse P, Bramanti P, di Bella P, Genton P.

Epilepsia. 2009 Jun;50(6):1587-95. doi: 10.1111/j.1528-1167.2008.01944.x. Epub 2009 Jan 31.

49.

Neuropsychological findings in patients with Unverricht-Lundborg disease.

Ferlazzo E, Gagliano A, Calarese T, Magaudda A, Striano P, Cortese L, Cedro C, Laguitton V, Bramanti P, Carbonaro M, Albachiara A, Fragassi N, Italiano D, Sessa E, Coppola A, Genton P.

Epilepsy Behav. 2009 Mar;14(3):545-9. doi: 10.1016/j.yebeh.2009.01.001. Epub 2009 Jan 29.

PMID:
19185615
50.

15q13.3 microdeletions increase risk of idiopathic generalized epilepsy.

Helbig I, Mefford HC, Sharp AJ, Guipponi M, Fichera M, Franke A, Muhle H, de Kovel C, Baker C, von Spiczak S, Kron KL, Steinich I, Kleefuss-Lie AA, Leu C, Gaus V, Schmitz B, Klein KM, Reif PS, Rosenow F, Weber Y, Lerche H, Zimprich F, Urak L, Fuchs K, Feucht M, Genton P, Thomas P, Visscher F, de Haan GJ, Møller RS, Hjalgrim H, Luciano D, Wittig M, Nothnagel M, Elger CE, Nürnberg P, Romano C, Malafosse A, Koeleman BP, Lindhout D, Stephani U, Schreiber S, Eichler EE, Sander T.

Nat Genet. 2009 Feb;41(2):160-2. doi: 10.1038/ng.292. Epub 2009 Jan 11.

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