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[Management of the first nonfebrile seizure in infants and children].
Auvin S, Walls E, Sabouraud P, Bednarek N, Villeneuve N, Vallée L; Commission épilepsie de la Société française de neurologie pédiatrique. Auvin S, et al. Among authors: villeneuve n. Arch Pediatr. 2008 Nov;15(11):1677-84. doi: 10.1016/j.arcped.2008.08.019. Epub 2008 Oct 2. Arch Pediatr. 2008. PMID: 18835140 French.
The ketogenic diet improves recently worsened focal epilepsy.
Villeneuve N, Pinton F, Bahi-Buisson N, Dulac O, Chiron C, Nabbout R. Villeneuve N, et al. Dev Med Child Neurol. 2009 Apr;51(4):276-81. doi: 10.1111/j.1469-8749.2008.03216.x. Epub 2008 Feb 3. Dev Med Child Neurol. 2009. PMID: 19191829 Free article.
Epileptic and nonepileptic features in patients with early onset epileptic encephalopathy and STXBP1 mutations.
Milh M, Villeneuve N, Chouchane M, Kaminska A, Laroche C, Barthez MA, Gitiaux C, Bartoli C, Borges-Correia A, Cacciagli P, Mignon-Ravix C, Cuberos H, Chabrol B, Villard L. Milh M, et al. Among authors: villeneuve n. Epilepsia. 2011 Oct;52(10):1828-34. doi: 10.1111/j.1528-1167.2011.03181.x. Epub 2011 Jul 19. Epilepsia. 2011. PMID: 21770924 Free article.
Recurrent mutations in the CDKL5 gene: genotype-phenotype relationships.
Bahi-Buisson N, Villeneuve N, Caietta E, Jacquette A, Maurey H, Matthijs G, Van Esch H, Delahaye A, Moncla A, Milh M, Zufferey F, Diebold B, Bienvenu T. Bahi-Buisson N, et al. Among authors: villeneuve n. Am J Med Genet A. 2012 Jul;158A(7):1612-9. doi: 10.1002/ajmg.a.35401. Epub 2012 Jun 7. Am J Med Genet A. 2012. PMID: 22678952
[Epilepsy and mitochondrial diseases: retrospective study on 53 epileptic children].
Caietta E, Cano A, Halbert C, Hugonenq C, Mancini J, Milh M, Lépine A, Villeneuve N, Chaussenot A, Paquis-Flucklinger V, Chabrol B. Caietta E, et al. Among authors: villeneuve n. Arch Pediatr. 2012 Aug;19(8):794-802. doi: 10.1016/j.arcped.2012.05.004. Epub 2012 Jul 11. Arch Pediatr. 2012. PMID: 22789745 French.
Similar early characteristics but variable neurological outcome of patients with a de novo mutation of KCNQ2.
Milh M, Boutry-Kryza N, Sutera-Sardo J, Mignot C, Auvin S, Lacoste C, Villeneuve N, Roubertie A, Heron B, Carneiro M, Kaminska A, Altuzarra C, Blanchard G, Ville D, Barthez MA, Heron D, Gras D, Afenjar A, Dorison N, Doummar D, Billette de Villemeur T, An I, Jacquette A, Charles P, Perrier J, Isidor B, Vercueil L, Chabrol B, Badens C, Lesca G, Villard L. Milh M, et al. Among authors: villeneuve n. Orphanet J Rare Dis. 2013 May 22;8:80. doi: 10.1186/1750-1172-8-80. Orphanet J Rare Dis. 2013. PMID: 23692823 Free PMC article.
Cortical involvement in focal epilepsies with epileptic spasms.
de la Vaissière S, Milh M, Scavarda D, Carron R, Lépine A, Trébuchon A, Gavaret M, Hewett R, Laguitton V, Daquin G, Villeneuve N, Bartolomei F. de la Vaissière S, et al. Among authors: villeneuve n. Epilepsy Res. 2014 Nov;108(9):1572-80. doi: 10.1016/j.eplepsyres.2014.08.008. Epub 2014 Aug 30. Epilepsy Res. 2014. PMID: 25212728
Epilepsy diagnostic and treatment needs identified with a collaborative database involving tertiary centers in France.
Chipaux M, Szurhaj W, Vercueil L, Milh M, Villeneuve N, Cances C, Auvin S, Chassagnon S, Napuri S, Allaire C, Derambure P, Marchal C, Caubel I, Ricard-Mousnier B, N'Guyen The Tich S, Pinard JM, Bahi-Buisson N, de Baracé C, Kahane P, Gautier A, Hamelin S, Coste-Zeitoun D, Rosenberg SD, Clerson P, Nabbout R, Kuchenbuch M, Picot MC, Kaminska A; GRENAT Group. Chipaux M, et al. Among authors: n guyen the tich s, villeneuve n. Epilepsia. 2016 May;57(5):757-69. doi: 10.1111/epi.13368. Epub 2016 Apr 1. Epilepsia. 2016. PMID: 27037674 Free article.
155 results