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Page 1
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
Levodopa-responsive dystonia. GTP cyclohydrolase I or parkin mutations?
Tassin J, Dürr A, Bonnet AM, Gil R, Vidailhet M, Lücking CB, Goas JY, Durif F, Abada M, Echenne B, Motte J, Lagueny A, Lacomblez L, Jedynak P, Bartholomé B, Agid Y, Brice A. Tassin J, et al. Among authors: vidailhet m. Brain. 2000 Jun;123 ( Pt 6):1112-21. doi: 10.1093/brain/123.6.1112. Brain. 2000. PMID: 10825351
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.
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
How much phenotypic variation can be attributed to parkin genotype?
Lohmann E, Periquet M, Bonifati V, Wood NW, De Michele G, Bonnet AM, Fraix V, Broussolle E, Horstink MW, Vidailhet M, Verpillat P, Gasser T, Nicholl D, Teive H, Raskin S, Rascol O, Destée A, Ruberg M, Gasparini F, Meco G, Agid Y, Durr A, Brice A; French Parkinson's Disease Genetics Study Group; European Consortium on Genetic Susceptibility in Parkinson's Disease. Lohmann E, et al. Among authors: vidailhet m. Ann Neurol. 2003 Aug;54(2):176-85. doi: 10.1002/ana.10613. Ann Neurol. 2003. PMID: 12891670
Candidate gene studies in focal dystonia.
Sibbing D, Asmus F, König IR, Tezenas du Montcel S, Vidailhet M, Sangla S, Oertel WH, Brice A, Ziegler A, Gasser T, Bandmann O. Sibbing D, et al. Among authors: vidailhet m. Neurology. 2003 Oct 28;61(8):1097-101. doi: 10.1212/01.wnl.0000090560.20641.ab. Neurology. 2003. PMID: 14581671
Disorganized somatotopy in the putamen of patients with focal hand dystonia.
Delmaire C, Krainik A, Tézenas du Montcel S, Gerardin E, Meunier S, Mangin JF, Sangla S, Garnero L, Vidailhet M, Lehéricy S. Delmaire C, et al. Among authors: vidailhet m. Neurology. 2005 Apr 26;64(8):1391-6. doi: 10.1212/01.WNL.0000158424.01299.76. Neurology. 2005. PMID: 15851729
712 results