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Page 1
De Novo Mutation in TMEM151A and Paroxysmal Kinesigenic Dyskinesia.
Wirth T, Méneret A, Drouot N, Rudolf G, Lagha Boukbiza O, Chelly J, Tranchant C, Piton A, Roze E, Anheim M. Wirth T, et al. Among authors: roze e. Mov Disord. 2022 May;37(5):1115-1117. doi: 10.1002/mds.29023. Mov Disord. 2022. PMID: 35587630 Free PMC article. No abstract available.
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
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
Myoclonus-dystonia: an update.
Kinugawa K, Vidailhet M, Clot F, Apartis E, Grabli D, Roze E. Kinugawa K, et al. Among authors: roze e. Mov Disord. 2009 Mar 15;24(4):479-89. doi: 10.1002/mds.22425. Mov Disord. 2009. PMID: 19117361 Review.
Table tennis dystonia.
Le Floch A, Vidailhet M, Flamand-Rouvière C, Grabli D, Mayer JM, Gonce M, Broussolle E, Roze E. Le Floch A, et al. Among authors: roze e. Mov Disord. 2010 Feb 15;25(3):394-7. doi: 10.1002/mds.22968. Mov Disord. 2010. PMID: 20108363
Symptomatic paroxysmal dysarthria-ataxia in demyelinating diseases.
Marcel C, Anheim M, Flamand-Rouvière C, Heran F, Masnou P, Boulay C, Mari I, Tranchant C, Roze E. Marcel C, et al. Among authors: roze e. J Neurol. 2010 Aug;257(8):1369-72. doi: 10.1007/s00415-010-5534-3. Epub 2010 Mar 30. J Neurol. 2010. PMID: 20352251
Myoclonus dystonia plus syndrome due to a novel 7q21 microdeletion.
Saugier-Veber P, Doummar D, Barthez MA, Czernecki V, Drouot N, Apartis E, Bürglen L, Frebourg T, Roze E. Saugier-Veber P, et al. Among authors: roze e. Am J Med Genet A. 2010 May;152A(5):1244-9. doi: 10.1002/ajmg.a.33369. Am J Med Genet A. 2010. PMID: 20425829
Speech disturbances in patients with dystonia or chorea due to neurometabolic disorders.
Flamand-Rouvière C, Guettard E, Moreau C, Bahi-Buisson N, Valayannopoulos V, Grabli D, Motte J, Rodriguez D, Roubertie A, Maintigneux L, Kemlin I, Ceballos-Picot I, Adams D, Vidailhet M, Roze E. Flamand-Rouvière C, et al. Among authors: roze e. Mov Disord. 2010 Aug 15;25(11):1605-11. doi: 10.1002/mds.23134. Mov Disord. 2010. PMID: 20629163
362 results