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PRRT2 mutations: a major cause of paroxysmal kinesigenic dyskinesia in the European population.
Méneret A, Grabli D, Depienne C, Gaudebout C, Picard F, Dürr A, Lagroua I, Bouteiller D, Mignot C, Doummar D, Anheim M, Tranchant C, Burbaud P, Jedynak CP, Gras D, Steschenko D, Devos D, Billette de Villemeur T, Vidailhet M, Brice A, Roze E. Méneret A, et al. Among authors: vidailhet m. Neurology. 2012 Jul 10;79(2):170-4. doi: 10.1212/WNL.0b013e31825f06c3. Epub 2012 Jun 27. Neurology. 2012. PMID: 22744660
[Propriospinal myoclonus in a HIV seropositive patient].
Lubetzki C, Vidailhet M, Jedynak CP, Thibault S, Mrejen S, Vittecoq D, Chain F. Lubetzki C, et al. Among authors: vidailhet m. Rev Neurol (Paris). 1994;150(1):70-2. Rev Neurol (Paris). 1994. PMID: 7801045 French.
[Dystonia].
Vidailhet M, Jedynak CP. Vidailhet M, et al. Rev Prat. 1997 May 15;47(10):1088-93. Rev Prat. 1997. PMID: 9208672 French.
[Tremors].
Jedynak CP, Vidailhet M. Jedynak CP, et al. Among authors: vidailhet m. Rev Prat. 1997 May 15;47(10):1098-102. Rev Prat. 1997. PMID: 9208674 Review. French.
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.
Pathology of symptomatic tremors.
Vidailhet M, Jedynak CP, Pollak P, Agid Y. Vidailhet M, et al. Mov Disord. 1998;13 Suppl 3:49-54. doi: 10.1002/mds.870131309. Mov Disord. 1998. PMID: 9827595 Review.
712 results