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Page 1
Effects of gender on the phenotype of CADASIL.
Gunda B, Hervé D, Godin O, Bruno M, Reyes S, Alili N, Opherk C, Jouvent E, Düring M, Bousser MG, Dichgans M, Chabriat H. Gunda B, et al. Among authors: alili n. Stroke. 2012 Jan;43(1):137-41. doi: 10.1161/STROKEAHA.111.631028. Epub 2011 Oct 27. Stroke. 2012. PMID: 22033996
Prevalence and characteristics of migraine in CADASIL.
Guey S, Mawet J, Hervé D, Duering M, Godin O, Jouvent E, Opherk C, Alili N, Dichgans M, Chabriat H. Guey S, et al. Among authors: alili n. Cephalalgia. 2016 Oct;36(11):1038-1047. doi: 10.1177/0333102415620909. Epub 2016 Jul 11. Cephalalgia. 2016. PMID: 26646784
Phenotypic variability in 446 CADASIL patients: Impact of NOTCH3 gene mutation location in addition to the effects of age, sex and vascular risk factors.
Dupé C, Guey S, Biard L, Dieng S, Lebenberg J, Grosset L, Alili N, Hervé D, Tournier-Lasserve E, Jouvent E, Chevret S, Chabriat H. Dupé C, et al. Among authors: alili n. J Cereb Blood Flow Metab. 2023 Jan;43(1):153-166. doi: 10.1177/0271678X221126280. Epub 2022 Oct 17. J Cereb Blood Flow Metab. 2023. PMID: 36254369 Free PMC article.
The Epidermal Growth Factor Domain of the Mutation Does Not Appear to Influence Disease Progression in CADASIL When Brain Volume and Sex Are Taken into Account.
Lebenberg J, Guichard JP, Guillonnet A, Hervé D, Alili N, Taleb A, Dias-Gastellier N, Chabriat H, Jouvent E. Lebenberg J, et al. Among authors: alili n. AJNR Am J Neuroradiol. 2022 May;43(5):715-720. doi: 10.3174/ajnr.A7499. Epub 2022 Apr 29. AJNR Am J Neuroradiol. 2022. PMID: 35487587 Free PMC article.
A novel hereditary extensive vascular leukoencephalopathy mapping to chromosome 20q13.
Hervé D, Chabriat H, Rigal M, Dalloz MA, Kawkabani Marchini A, De Lepeleire J, Fontaine B, Ceuterick-de Groote C, Alili N, Mine M, Delaforge A, Bousser MG, Guichard JP, Martin JJ, Gray F, Tournier-Lasserve E. Hervé D, et al. Among authors: alili n. Neurology. 2012 Dec 4;79(23):2283-7. doi: 10.1212/WNL.0b013e3182768954. Epub 2012 Nov 21. Neurology. 2012. PMID: 23175731
A hereditary moyamoya syndrome with multisystemic manifestations.
Hervé D, Touraine P, Verloes A, Miskinyte S, Krivosic V, Logeart D, Alili N, Laredo JD, Gaudric A, Houdart E, Metzger JP, Tournier-Lasserve E, Woimant F. Hervé D, et al. Among authors: alili n. Neurology. 2010 Jul 20;75(3):259-64. doi: 10.1212/WNL.0b013e3181e8ee3f. Neurology. 2010. PMID: 20644152
Psychological impact of COVID-19 containment on CADASIL patients.
Reyes S, Jabouley A, Alili N, De Sanctis MH, Machado C, Taleb A, Herve D, Dias-Gastellier N, Chabriat H. Reyes S, et al. Among authors: alili n. J Neurol. 2023 May;270(5):2370-2379. doi: 10.1007/s00415-023-11648-8. Epub 2023 Mar 4. J Neurol. 2023. PMID: 36869886 Free PMC article.
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