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PRRT2 mutations and paroxysmal disorders.
Méneret A, Gaudebout C, Riant F, Vidailhet M, Depienne C, Roze E. Méneret A, et al. Among authors: riant f. Eur J Neurol. 2013 Jun;20(6):872-8. doi: 10.1111/ene.12104. Epub 2013 Feb 9. Eur J Neurol. 2013. PMID: 23398397 Review.
Genotype-phenotype correlations in cerebral cavernous malformations patients.
Denier C, Labauge P, Bergametti F, Marchelli F, Riant F, Arnoult M, Maciazek J, Vicaut E, Brunereau L, Tournier-Lasserve E; Société Française de Neurochirurgie. Denier C, et al. Among authors: riant f. Ann Neurol. 2006 Nov;60(5):550-6. doi: 10.1002/ana.20947. Ann Neurol. 2006. PMID: 17041941
Late onset hereditary episodic ataxia.
Damak M, Riant F, Boukobza M, Tournier-Lasserve E, Bousser MG, Vahedi K. Damak M, et al. Among authors: riant f. J Neurol Neurosurg Psychiatry. 2009 May;80(5):566-8. doi: 10.1136/jnnp.2008.150615. J Neurol Neurosurg Psychiatry. 2009. PMID: 19372292
Multiple dural lesions mimicking meningiomas in patients with CCM3/PDCD10 mutations.
Labauge P, Fontaine B, Neau JP, Bergametti F, Riant F, Blecon A, Marchelli F, Arnoult M, Lannuzel A, Clanet M, Olschwang S, Denier C, Tournier-Lasserve E. Labauge P, et al. Among authors: riant f. Neurology. 2009 Jun 9;72(23):2044-6. doi: 10.1212/WNL.0b013e3181a92b13. Neurology. 2009. PMID: 19506228 No abstract available.
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