Vidailhet M - Search Results

1

Brain atrophy in prodromal synucleinopathy is shaped by structural connectivity and gene expression.

Rahayel S, Tremblay C, Vo A, Zheng YQ, Lehéricy S, Arnulf I, Vidailhet M, Corvol JC; ICEBERG Study Group; Gagnon JF, Postuma RB, Montplaisir J, Lewis S, Matar E, Ehgoetz Martens K, Borghammer P, Knudsen K, Hansen A, Monchi O, Misic B, Dagher A. Rahayel S, et al. Among authors: vidailhet m. Brain. 2022 Sep 14;145(9):3162-3178. doi: 10.1093/brain/awac187. Brain. 2022. PMID: 35594873

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

Pallidal stimulation for Parkinson's disease. Two targets?

Bejjani B, Damier P, Arnulf I, Bonnet AM, Vidailhet M, Dormont D, Pidoux B, Cornu P, Marsault C, Agid Y. Bejjani B, et al. Among authors: vidailhet m. Neurology. 1997 Dec;49(6):1564-9. doi: 10.1212/wnl.49.6.1564. Neurology. 1997. PMID: 9409347

4

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

5

Eye movement disorders in corticobasal degeneration.

Vidailhet M, Rivaud-Péchoux S. Vidailhet M, et al. Adv Neurol. 2000;82:161-7. Adv Neurol. 2000. PMID: 10624480 Review. No abstract available.

6

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

7

Longitudinal ocular motor study in corticobasal degeneration and progressive supranuclear palsy.

Rivaud-Péchoux S, Vidailhet M, Gallouedec G, Litvan I, Gaymard B, Pierrot-Deseilligny C. Rivaud-Péchoux S, et al. Among authors: vidailhet m. Neurology. 2000 Mar 14;54(5):1029-32. doi: 10.1212/wnl.54.5.1029. Neurology. 2000. PMID: 10720270

8

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

9

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

10

Clinical characteristics and topography of lesions in movement disorders due to thalamic lesions.

Lehéricy S, Grand S, Pollak P, Poupon F, Le Bas JF, Limousin P, Jedynak P, Marsault C, Agid Y, Vidailhet M. Lehéricy S, et al. Among authors: vidailhet m. Neurology. 2001 Sep 25;57(6):1055-66. doi: 10.1212/wnl.57.6.1055. Neurology. 2001. PMID: 11571334

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

725 results

Search Page

Filters