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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: opherk c. Stroke. 2012 Jan;43(1):137-41. doi: 10.1161/STROKEAHA.111.631028. Epub 2011 Oct 27. Stroke. 2012. PMID: 22033996
Genome-wide genotyping demonstrates a polygenic risk score associated with white matter hyperintensity volume in CADASIL.
Opherk C, Gonik M, Duering M, Malik R, Jouvent E, Hervé D, Adib-Samii P, Bevan S, Pianese L, Silvestri S, Dotti MT, De Stefano N, Liem M, Boon EM, Pescini F, Pachai C, Bracoud L, Müller-Myhsok B, Meitinger T, Rost N, Pantoni L, Lesnik Oberstein S, Federico A, Ragno M, Markus HS, Tournier-Lasserve E, Rosand J, Chabriat H, Dichgans M. Opherk C, et al. Stroke. 2014 Apr;45(4):968-72. doi: 10.1161/STROKEAHA.113.004461. Epub 2014 Feb 27. Stroke. 2014. PMID: 24578207 Free article.
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: opherk c. Cephalalgia. 2016 Oct;36(11):1038-1047. doi: 10.1177/0333102415620909. Epub 2016 Jul 11. Cephalalgia. 2016. PMID: 26646784
The effect of NOTCH3 pathogenic variant position on CADASIL disease severity: NOTCH3 EGFr 1-6 pathogenic variant are associated with a more severe phenotype and lower survival compared with EGFr 7-34 pathogenic variant.
Rutten JW, Van Eijsden BJ, Duering M, Jouvent E, Opherk C, Pantoni L, Federico A, Dichgans M, Markus HS, Chabriat H, Lesnik Oberstein SAJ. Rutten JW, et al. Among authors: opherk c. Genet Med. 2019 Mar;21(3):676-682. doi: 10.1038/s41436-018-0088-3. Epub 2018 Jul 22. Genet Med. 2019. PMID: 30032161 Free PMC article.
76 results