Singing in the brain: a new form of complex partial seizure?

Por Vidailhet, M, Serdaru, M, Agid, Y
Publicado em 1989

Cerebral Erdheim-Chester disease: report of two cases with progressive cerebellar syndrome with dentate abnormalities on magnetic resonance imaging

Por Pautas, E., Cherin, P., Pelletier, S., Vidailhet, M., Herson, S.
Publicado em 1998

The IMAO-B MDL 72.974 A in Parkinson's disease.

Por Marconi, R, Bonnet, A M, Vidailhet, M, Agid, Y
Publicado em 1992

Mirror movements of the non-affected hand in hemiparkinsonian patients: a reflection of ipsilateral motor overactivity?

Por Vidal, J, Derkinderen, P, Vidailhet, M, Thobois, S, Broussolle, E
Publicado em 2003

Alteration of substrate specificity by a naturally-occurring aldolase B mutation (Ala337-->Val) in fructose intolerance.

Por Rellos, P, Ali, M, Vidailhet, M, Sygusch, J, Cox, T M
Publicado em 1999

Factors predicting improvement in motor disability in writer's cramp treated with botulinum toxin

Por Djebbari, R, du Montcel, S T, Sangla, S, Vidal, J, Gallouedec, G, Vidailhet, M
Publicado em 2004

Overactivity of cervical premotor neurons in Parkinson's disease

Por Pol, S, Vidailhet, M, Meunier, S, Mazevet, D, Agid, Y, Pierrot-Deseillig..., E
Publicado em 1998

Does ageing aggravate parkinsonian disability?

Por Blin, J, Dubois, B, Bonnet, A M, Vidailhet, M, Brandabur, M, Agid, Y
Publicado em 1991

Cerebellar Processing of Sensory Inputs Primes Motor Cortex Plasticity

Por Popa, T., Velayudhan, B., Hubsch, C., Pradeep, S., Roze, E., Vidailhet, M., Meunier, S., Kishore, A.
Publicado em 2013

Familial Parkinson's disease and polymorphism at the CYP2D6 locus.

Por Mazzetti, P, Le Guern, E, Bonnet, A M, Vidailhet, M, Brice, A, Agid, Y
Publicado em 1994

Increased plasma neurotensin concentrations in patients with Parkinson's disease

Por Schimpff, R, Avard, C, Fenelon, G, Lhiaubet, A, Tenneze, L, Vidailhet, M, Rostene, W
Publicado em 2001

Autosomal dominant paroxysmal kinesigenic choreoathetosis: a clinical and genetic study of two families

Por PICARD, F, TASSIN, J, VIDAILHET, M, MARESCAUX, C, PICARD, F, AGID, Y, BRICE, A
Publicado em 1998

Null alleles of the aldolase B gene in patients with hereditary fructose intolerance.

Por Ali, M, Tunçman, G, Cross, N C, Vidailhet, M, Bökesoy, I, Gitzelmann, R, Cox, T M
Publicado em 1994

Neuropsychological pattern of striatonigral degeneration: comparison with Parkinson's disease and progressive supranuclear palsy.

Por Pillon, B, Gouider-Khouja, N, Deweer, B, Vidailhet, M, Malapani, C, Dubois, B, Agid, Y
Publicado em 1995

MRI in 31 patients with Behçet's disease and neurological involvement: prospective study with clinical correlation.

Por Wechsler, B, Dell'lsola, B, Vidailhet, M, Dormont, D, Piette, J C, Blétry, O, Godeau, P
Publicado em 1993

Saccade disturbances after bilateral lentiform nucleus lesions in humans.

Por Vermersch, A I, Müri, R M, Rivaud, S, Vidailhet, M, Gaymard, B, Agid, Y, Pierrot-Deseilligny, C
Publicado em 1996

Movement disorders as a new neurological clinical picture in severe SARS‐CoV‐2 infection

Por Cuhna, P., Herlin, B., Vassilev, K., Kas, A., Lehericy, S., Worbe, Y., Apartis, E., Vidailhet, M., Dupont, S.
Publicado no Eur J Neurol (2020)

Arbitrarily primed polymerase chain reaction as a rapid method to differentiate crossed from independent Pseudomonas cepacia infections in cystic fibrosis patients.

Por Bingen, E H, Weber, M, Derelle, J, Brahimi, N, Lambert-Zechovsky, N Y, Vidailhet, M, Navarro, J, Elion, J
Publicado em 1993

Efficacy of pallidal stimulation in isolated dystonia: a systematic review and meta‐analysis

Por Moro, E., LeReun, C., Krauss, J. K., Albanese, A., Lin, J.‐P., Walleser Autiero, S., Brionne, T. C., Vidailhet, M.
Publicado no Eur J Neurol (2017)

Comparative Study of MRI Biomarkers in the Substantia Nigra to Discriminate Idiopathic Parkinson Disease

Por Pyatigorskaya, N., Magnin, B., Mongin, M., Yahia-Cherif, L., Valabregue, R., Arnaldi, D., Ewenczyk, C., Poupon, C., Vidailhet, M., Lehéricy, S.
Publicado no AJNR Am J Neuroradiol (2018)