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378 results

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Page 1
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.
The adolescent and adult form of cobalamin C disease: clinical and molecular spectrum.
Thauvin-Robinet C, Roze E, Couvreur G, Horellou MH, Sedel F, Grabli D, Bruneteau G, Tonneti C, Masurel-Paulet A, Perennou D, Moreau T, Giroud M, de Baulny HO, Giraudier S, Faivre L. Thauvin-Robinet C, et al. Among authors: roze e. J Neurol Neurosurg Psychiatry. 2008 Jun;79(6):725-8. doi: 10.1136/jnnp.2007.133025. Epub 2008 Feb 1. J Neurol Neurosurg Psychiatry. 2008. PMID: 18245139
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.
Exhaustive analysis of BH4 and dopamine biosynthesis genes in patients with Dopa-responsive dystonia.
Clot F, Grabli D, Cazeneuve C, Roze E, Castelnau P, Chabrol B, Landrieu P, Nguyen K, Ponsot G, Abada M, Doummar D, Damier P, Gil R, Thobois S, Ward AJ, Hutchinson M, Toutain A, Picard F, Camuzat A, Fedirko E, Sân C, Bouteiller D, LeGuern E, Durr A, Vidailhet M, Brice A; French Dystonia Network. Clot F, et al. Among authors: roze e. Brain. 2009 Jul;132(Pt 7):1753-63. doi: 10.1093/brain/awp084. Epub 2009 Jun 2. Brain. 2009. PMID: 19491146
Pathophysiology of dystonia.
Vidailhet M, Grabli D, Roze E. Vidailhet M, et al. Among authors: roze e. Curr Opin Neurol. 2009 Aug;22(4):406-13. doi: 10.1097/WCO.0b013e32832d9ef3. Curr Opin Neurol. 2009. PMID: 19512924 Review.
Huntington's disease.
Roze E, Bonnet C, Betuing S, Caboche J. Roze E, et al. Adv Exp Med Biol. 2010;685:45-63. Adv Exp Med Biol. 2010. PMID: 20687494 Review.
[Movement disorders and neurometabolic diseases].
Grabli D, Auré K, Roze E. Grabli D, et al. Among authors: roze e. Rev Neurol (Paris). 2011 Feb;167(2):123-34. doi: 10.1016/j.neurol.2010.07.022. Epub 2010 Nov 17. Rev Neurol (Paris). 2011. PMID: 21087782 Review. French.
378 results