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

di Vidailhet, M, Serdaru, M, Agid, Y
Pubblicazione 1989

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

di Pautas, E., Cherin, P., Pelletier, S., Vidailhet, M., Herson, S.
Pubblicazione 1998

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

di Marconi, R, Bonnet, A M, Vidailhet, M, Agid, Y
Pubblicazione 1992

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

di Vidal, J, Derkinderen, P, Vidailhet, M, Thobois, S, Broussolle, E
Pubblicazione 2003

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

di Rellos, P, Ali, M, Vidailhet, M, Sygusch, J, Cox, T M
Pubblicazione 1999

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

di Djebbari, R, du Montcel, S T, Sangla, S, Vidal, J, Gallouedec, G, Vidailhet, M
Pubblicazione 2004

Overactivity of cervical premotor neurons in Parkinson's disease

di Pol, S, Vidailhet, M, Meunier, S, Mazevet, D, Agid, Y, Pierrot-Deseillig..., E
Pubblicazione 1998

Does ageing aggravate parkinsonian disability?

di Blin, J, Dubois, B, Bonnet, A M, Vidailhet, M, Brandabur, M, Agid, Y
Pubblicazione 1991

Cerebellar Processing of Sensory Inputs Primes Motor Cortex Plasticity

di Popa, T., Velayudhan, B., Hubsch, C., Pradeep, S., Roze, E., Vidailhet, M., Meunier, S., Kishore, A.
Pubblicazione 2013

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

di Mazzetti, P, Le Guern, E, Bonnet, A M, Vidailhet, M, Brice, A, Agid, Y
Pubblicazione 1994

Increased plasma neurotensin concentrations in patients with Parkinson's disease

di Schimpff, R, Avard, C, Fenelon, G, Lhiaubet, A, Tenneze, L, Vidailhet, M, Rostene, W
Pubblicazione 2001

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

di PICARD, F, TASSIN, J, VIDAILHET, M, MARESCAUX, C, PICARD, F, AGID, Y, BRICE, A
Pubblicazione 1998

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

di Ali, M, Tunçman, G, Cross, N C, Vidailhet, M, Bökesoy, I, Gitzelmann, R, Cox, T M
Pubblicazione 1994

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

di Pillon, B, Gouider-Khouja, N, Deweer, B, Vidailhet, M, Malapani, C, Dubois, B, Agid, Y
Pubblicazione 1995

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

di Wechsler, B, Dell'lsola, B, Vidailhet, M, Dormont, D, Piette, J C, Blétry, O, Godeau, P
Pubblicazione 1993

Saccade disturbances after bilateral lentiform nucleus lesions in humans.

di Vermersch, A I, Müri, R M, Rivaud, S, Vidailhet, M, Gaymard, B, Agid, Y, Pierrot-Deseilligny, C
Pubblicazione 1996

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

di Cuhna, P., Herlin, B., Vassilev, K., Kas, A., Lehericy, S., Worbe, Y., Apartis, E., Vidailhet, M., Dupont, S.
Pubblicato in 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.

di Bingen, E H, Weber, M, Derelle, J, Brahimi, N, Lambert-Zechovsky, N Y, Vidailhet, M, Navarro, J, Elion, J
Pubblicazione 1993

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

di Moro, E., LeReun, C., Krauss, J. K., Albanese, A., Lin, J.‐P., Walleser Autiero, S., Brionne, T. C., Vidailhet, M.
Pubblicato in Eur J Neurol (2017)

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

di Pyatigorskaya, N., Magnin, B., Mongin, M., Yahia-Cherif, L., Valabregue, R., Arnaldi, D., Ewenczyk, C., Poupon, C., Vidailhet, M., Lehéricy, S.
Pubblicato in AJNR Am J Neuroradiol (2018)