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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: roze e. 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.
Epsilon sarcoglycan mutations and phenotype in French patients with myoclonic syndromes.
Tezenas du Montcel S, Clot F, Vidailhet M, Roze E, Damier P, Jedynak CP, Camuzat A, Lagueny A, Vercueil L, Doummar D, Guyant-Maréchal L, Houeto JL, Ponsot G, Thobois S, Cournelle MA, Durr A, Durif F, Echenne B, Hannequin D, Tranchant C, Brice A; French Dystonia Network. Tezenas du Montcel S, et al. Among authors: roze e. J Med Genet. 2006 May;43(5):394-400. doi: 10.1136/jmg.2005.036780. Epub 2005 Oct 14. J Med Genet. 2006. PMID: 16227522 Free PMC article.
Interictal myoclonus with paroxysmal kinesigenic dyskinesia.
Cochen De Cock V, Bourdain F, Apartis E, Trocello JM, Roze E, Vidailhet M. Cochen De Cock V, et al. Among authors: roze e. Mov Disord. 2006 Sep;21(9):1533-5. doi: 10.1002/mds.20992. Mov Disord. 2006. PMID: 16763976
362 results