Vidailhet M - Search Results

1

Striatal and cerebellar vesicular acetylcholine transporter expression is disrupted in human DYT1 dystonia.

Mazere J, Dilharreguy B, Catheline G, Vidailhet M, Deffains M, Vimont D, Ribot B, Barse E, Cif L, Mazoyer B, Langbour N, Pisani A, Allard M, Lamare F, Guehl D, Fernandez P, Burbaud P. Mazere J, et al. Among authors: vidailhet m. Brain. 2021 Apr 12;144(3):909-923. doi: 10.1093/brain/awaa465. Brain. 2021. PMID: 33638639

2

Striatopallidal and thalamic dystonia. A magnetic resonance imaging anatomoclinical study.

Lehéricy S, Vidailhet M, Dormont D, Piérot L, Chiras J, Mazetti P, Marsault C, Agid Y. Lehéricy S, et al. Among authors: vidailhet m. Arch Neurol. 1996 Mar;53(3):241-50. doi: 10.1001/archneur.1996.00550030051022. Arch Neurol. 1996. PMID: 8651877

3

DYT1 mutation in French families with idiopathic torsion dystonia.

Lebre AS, Durr A, Jedynak P, Ponsot G, Vidailhet M, Agid Y, Brice A. Lebre AS, et al. Among authors: vidailhet m. Brain. 1999 Jan;122 ( Pt 1):41-5. doi: 10.1093/brain/122.1.41. Brain. 1999. PMID: 10050893

4

Frequency of the DYT1 mutation in primary torsion dystonia without family history.

Brassat D, Camuzat A, Vidailhet M, Feki I, Jedynak P, Klap P, Agid Y, Dürr A, Brice A. Brassat D, et al. Among authors: vidailhet m. Arch Neurol. 2000 Mar;57(3):333-5. doi: 10.1001/archneur.57.3.333. Arch Neurol. 2000. PMID: 10714658

5

A major locus for several phenotypes of myoclonus--dystonia on chromosome 7q.

Vidailhet M, Tassin J, Durif F, Nivelon-Chevallier A, Agid Y, Brice A, Dürr A. Vidailhet M, et al. Neurology. 2001 May 8;56(9):1213-6. doi: 10.1212/wnl.56.9.1213. Neurology. 2001. PMID: 11342690

6

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

7

Globus pallidus internus stimulation in primary generalized dystonia: a H215O PET study.

Detante O, Vercueil L, Thobois S, Broussolle E, Costes N, Lavenne F, Chabardes S, Lebars D, Vidailhet M, Benabid AL, Pollak P. Detante O, et al. Among authors: vidailhet m. Brain. 2004 Aug;127(Pt 8):1899-908. doi: 10.1093/brain/awh213. Epub 2004 Jul 1. Brain. 2004. PMID: 15231585

8

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

9

Recessive hereditary methaemoglobinaemia, type II: delineation of the clinical spectrum.

Ewenczyk C, Leroux A, Roubergue A, Laugel V, Afenjar A, Saudubray JM, Beauvais P, Billette de Villemeur T, Vidailhet M, Roze E. Ewenczyk C, et al. Among authors: vidailhet m. Brain. 2008 Mar;131(Pt 3):760-1. doi: 10.1093/brain/awm337. Epub 2008 Jan 17. Brain. 2008. PMID: 18202104 Review.

10

Is the early-onset torsion dystonia (EOTD) linked to TOR1A gene as frequent as expected in France?

Frédéric MY, Clot F, Cif L, Blanchard A, Dürr A, Vuillaume I, Lesca G, Kreisler A, Davin C, Besnard T, Rousset F, Thorel D, Saquet C, Mechin D, Ozelius L, Agid Y, Barroso B, Chabrol B, Chan V, Clanet M, Coubes C, Destee A, Nguyen K, Vial C, Vidailhet M, Xie J, Sablonniere B, Calender A, Brice A, Roubertie A, Coubes P, Claustres M, Tuffery-Giraud S, Collod-Beroud G. Frédéric MY, et al. Among authors: vidailhet m. Neurogenetics. 2008 May;9(2):143-50. doi: 10.1007/s10048-008-0123-7. Epub 2008 Mar 6. Neurogenetics. 2008. PMID: 18322712 Free article.

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