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Second consensus statement on the diagnosis of multiple system atrophy.
Gilman S, Wenning GK, Low PA, Brooks DJ, Mathias CJ, Trojanowski JQ, Wood NW, Colosimo C, Dürr A, Fowler CJ, Kaufmann H, Klockgether T, Lees A, Poewe W, Quinn N, Revesz T, Robertson D, Sandroni P, Seppi K, Vidailhet M. Gilman S, et al. Among authors: vidailhet m. Neurology. 2008 Aug 26;71(9):670-6. doi: 10.1212/01.wnl.0000324625.00404.15. Neurology. 2008. PMID: 18725592 Free PMC article.
D2 dopamine receptor gene in myoclonic dystonia and essential myoclonus.
Dürr A, Tassin J, Vidailhet M, Durif F, Jedynak P, Agid Y, Brice A. Dürr A, et al. Among authors: vidailhet m. Ann Neurol. 2000 Jul;48(1):127-8. doi: 10.1002/1531-8249(200007)48:1<127::aid-ana24>3.3.co;2-4. Ann Neurol. 2000. PMID: 10894231 No abstract available.
Myoclonus-dystonia syndrome: epsilon-sarcoglycan mutations and phenotype.
Asmus F, Zimprich A, Tezenas Du Montcel S, Kabus C, Deuschl G, Kupsch A, Ziemann U, Castro M, Kühn AA, Strom TM, Vidailhet M, Bhatia KP, Dürr A, Wood NW, Brice A, Gasser T. Asmus F, et al. Among authors: vidailhet m. Ann Neurol. 2002 Oct;52(4):489-92. doi: 10.1002/ana.10325. Ann Neurol. 2002. PMID: 12325078
Parkin mutations are frequent in patients with isolated early-onset parkinsonism.
Periquet M, Latouche M, Lohmann E, Rawal N, De Michele G, Ricard S, Teive H, Fraix V, Vidailhet M, Nicholl D, Barone P, Wood NW, Raskin S, Deleuze JF, Agid Y, Dürr A, Brice A; French Parkinson's Disease Genetics Study Group; European Consortium on Genetic Susceptibility in Parkinson's Disease. Periquet M, et al. Among authors: vidailhet m. Brain. 2003 Jun;126(Pt 6):1271-8. doi: 10.1093/brain/awg136. Brain. 2003. PMID: 12764050
Myoclonus in spinal dysraphism.
Warren JE, Vidailhet M, Kneebone CS, Quinn NP, Thompson PD. Warren JE, et al. Among authors: vidailhet m. Mov Disord. 2003 Aug;18(8):961-4. doi: 10.1002/mds.10469. Mov Disord. 2003. PMID: 12889092
712 results