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Page 1
Characterization of Recessive Parkinson Disease in a Large Multicenter Study.
Lesage S, Lunati A, Houot M, Romdhan SB, Clot F, Tesson C, Mangone G, Toullec BL, Courtin T, Larcher K, Benmahdjoub M, Arezki M, Bouhouche A, Anheim M, Roze E, Viallet F, Tison F, Broussolle E, Emre M, Hanagasi H, Bilgic B, Tazir M, Djebara MB, Gouider R, Tranchant C, Vidailhet M, Le Guern E, Corti O, Mhiri C, Lohmann E, Singleton A, Corvol JC, Brice A; French Parkinson Disease Genetics Study Group. Lesage S, et al. Among authors: roze e. Ann Neurol. 2020 Oct;88(4):843-850. doi: 10.1002/ana.25787. Epub 2020 Jul 28. Ann Neurol. 2020. PMID: 33045815 Free PMC article.
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.
Head tremor in Parkinson's disease.
Roze E, Coêlho-Braga MC, Gayraud D, Legrand AP, Trocello JM, Fénelon G, Cochen V, Patte N, Viallet F, Vidailhet M, Pollak P, Apartis E. Roze E, et al. Mov Disord. 2006 Aug;21(8):1245-8. doi: 10.1002/mds.20918. Mov Disord. 2006. PMID: 16673401
Myoclonus-dystonia: clinical and electrophysiologic pattern related to SGCE mutations.
Roze E, Apartis E, Clot F, Dorison N, Thobois S, Guyant-Marechal L, Tranchant C, Damier P, Doummar D, Bahi-Buisson N, André-Obadia N, Maltete D, Echaniz-Laguna A, Pereon Y, Beaugendre Y, Dupont S, De Greslan T, Jedynak CP, Ponsot G, Dussaule JC, Brice A, Dürr A, Vidailhet M. Roze E, et al. Neurology. 2008 Mar 25;70(13):1010-6. doi: 10.1212/01.wnl.0000297516.98574.c0. Neurology. 2008. PMID: 18362280
[Pathophysiology of Huntington's disease: an update].
Roze E, Betuing S, Deyts C, Vidailhet M, Caboche J. Roze E, et al. Rev Neurol (Paris). 2008 Dec;164(12):977-94. doi: 10.1016/j.neurol.2008.03.006. Epub 2008 May 13. Rev Neurol (Paris). 2008. PMID: 18808762 Review. French.
Myoclonus-dystonia due to maternal uniparental disomy.
Guettard E, Portnoi MF, Lohmann-Hedrich K, Keren B, Rossignol S, Winkler S, El Kamel I, Leu S, Apartis E, Vidailhet M, Klein C, Roze E. Guettard E, et al. Among authors: roze e. Arch Neurol. 2008 Oct;65(10):1380-5. doi: 10.1001/archneur.65.10.1380. Arch Neurol. 2008. PMID: 18852357
374 results