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Page 1
A novel large deletion in CCM1 gene in a Tunisian family.
Tinsa F, Bel Hadj I, Riant F, Ben Romdhane M, Brini I, Tournier-Lasserve E, Louati H, Abdelhak S, Hamouda S, Boussetta K. Tinsa F, et al. Rev Neurol (Paris). 2019 Mar;175(3):194-197. doi: 10.1016/j.neurol.2018.04.013. Epub 2018 Oct 9. Rev Neurol (Paris). 2019. PMID: 30314744
[Hereditary episodic ataxia].
Riant F, Vahedi K, Tournier-Lasserve E. Riant F, et al. Rev Neurol (Paris). 2011 May;167(5):401-7. doi: 10.1016/j.neurol.2010.10.016. Epub 2011 Apr 13. Rev Neurol (Paris). 2011. PMID: 21492892 Review. French.
Late onset hereditary episodic ataxia.
Damak M, Riant F, Boukobza M, Tournier-Lasserve E, Bousser MG, Vahedi K. Damak M, et al. J Neurol Neurosurg Psychiatry. 2009 May;80(5):566-8. doi: 10.1136/jnnp.2008.150615. J Neurol Neurosurg Psychiatry. 2009. PMID: 19372292
A novel hereditary small vessel disease of the brain.
Verreault S, Joutel A, Riant F, Neves G, Rui Silva M, Maciazek J, Tournier-Lasserve E, Bousser MG, Chabriat H. Verreault S, et al. Ann Neurol. 2006 Feb;59(2):353-7. doi: 10.1002/ana.20775. Ann Neurol. 2006. PMID: 16404745
CCM3 Mutations Are Associated with Early-Onset Cerebral Hemorrhage and Multiple Meningiomas.
Riant F, Bergametti F, Fournier HD, Chapon F, Michalak-Provost S, Cecillon M, Lejeune P, Hosseini H, Choe C, Orth M, Bernreuther C, Boulday G, Denier C, Labauge P, Tournier-Lasserve E. Riant F, et al. Mol Syndromol. 2013 Apr;4(4):165-72. doi: 10.1159/000350042. Epub 2013 Apr 3. Mol Syndromol. 2013. PMID: 23801932 Free PMC article.
260 results