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A novel DCC mutation and genetic heterogeneity in congenital mirror movements.
Depienne C, Cincotta M, Billot S, Bouteiller D, Groppa S, Brochard V, Flamand C, Hubsch C, Meunier S, Giovannelli F, Klebe S, Corvol JC, Vidailhet M, Brice A, Roze E. Depienne C, et al. Among authors: vidailhet m. Neurology. 2011 Jan 18;76(3):260-4. doi: 10.1212/WNL.0b013e318207b1e0. Neurology. 2011. PMID: 21242494
Familial Parkinson's disease and polymorphism at the CYP2D6 locus.
Mazzetti P, Le Guern E, Bonnet AM, Vidailhet M, Brice A, Agid Y. Mazzetti P, et al. Among authors: vidailhet m. J Neurol Neurosurg Psychiatry. 1994 Jul;57(7):871-2. doi: 10.1136/jnnp.57.7.871. J Neurol Neurosurg Psychiatry. 1994. PMID: 8021689 Free PMC article. No abstract available.
Eye movements in parkinsonian syndromes.
Vidailhet M, Rivaud S, Gouider-Khouja N, Pillon B, Bonnet AM, Gaymard B, Agid Y, Pierrot-Deseilligny C. Vidailhet M, et al. Ann Neurol. 1994 Apr;35(4):420-6. doi: 10.1002/ana.410350408. Ann Neurol. 1994. PMID: 8154868
Overactivity of cervical premotor neurons in Parkinson's disease.
Pol S, Vidailhet M, Meunier S, Mazevet D, Agid Y, Pierrot-Deseilligny E. Pol S, et al. Among authors: vidailhet m. J Neurol Neurosurg Psychiatry. 1998 Feb;64(2):166-71. doi: 10.1136/jnnp.64.2.166. J Neurol Neurosurg Psychiatry. 1998. PMID: 9489525 Free PMC article.
Chromosome 6-linked autosomal recessive early-onset Parkinsonism: linkage in European and Algerian families, extension of the clinical spectrum, and evidence of a small homozygous deletion in one family. The French Parkinson's Disease Genetics Study Group, and the European Consortium on Genetic Susceptibility in Parkinson's Disease.
Tassin J, Dürr A, de Broucker T, Abbas N, Bonifati V, De Michele G, Bonnet AM, Broussolle E, Pollak P, Vidailhet M, De Mari M, Marconi R, Medjbeur S, Filla A, Meco G, Agid Y, Brice A. Tassin J, et al. Among authors: vidailhet m. Am J Hum Genet. 1998 Jul;63(1):88-94. doi: 10.1086/301934. Am J Hum Genet. 1998. PMID: 9634531 Free PMC article.
711 results