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EGR2 mutation enhances phenotype spectrum of Dejerine-Sottas syndrome.
Gargaun E, Seferian AM, Cardas R, Le Moing AG, Delanoe C, Nectoux J, Nelson I, Bonne G, Bihoreau MT, Deleuze JF, Boland A, Masson C, Servais L, Gidaro T. Gargaun E, et al. Among authors: delanoe c. J Neurol. 2016 Jul;263(7):1456-8. doi: 10.1007/s00415-016-8153-9. Epub 2016 May 9. J Neurol. 2016. PMID: 27159987 No abstract available.
Duplication of the 15q11-q13 region: clinical and genetic study of 30 new cases.
Al Ageeli E, Drunat S, Delanoë C, Perrin L, Baumann C, Capri Y, Fabre-Teste J, Aboura A, Dupont C, Auvin S, El Khattabi L, Chantereau D, Moncla A, Tabet AC, Verloes A. Al Ageeli E, et al. Among authors: delanoe c. Eur J Med Genet. 2014 Jan;57(1):5-14. doi: 10.1016/j.ejmg.2013.10.008. Epub 2013 Nov 12. Eur J Med Genet. 2014. PMID: 24239951
A case of Lennox-Gastaut syndrome in a patient with FOXG1-related disorder.
Terrone G, Bienvenu T, Germanaud D, Barthez-Carpentier MA, Diebold B, Delanoe C, Passemard S, Auvin S. Terrone G, et al. Among authors: delanoe c. Epilepsia. 2014 Nov;55(11):e116-9. doi: 10.1111/epi.12800. Epub 2014 Sep 29. Epilepsia. 2014. PMID: 25266269 Free article.
Neuropathology findings in KCNQ2 neonatal epileptic encephalopathy.
Legros L, Adle-Biassette H, Dozières-Puyravel B, Khung S, Elmaleh-Bergès M, Lesca G, Delanoë C, Biran V, Auvin S. Legros L, et al. Among authors: delanoe c. Seizure. 2022 Jul;99:36-39. doi: 10.1016/j.seizure.2022.05.008. Epub 2022 May 10. Seizure. 2022. PMID: 35584591 Free article.
45 results