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M Vidailhet

Showing results (291-300 of 303) with videos related to

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Annales De Biologie Clinique|July 31, 2002
[Vitamin deficiency and malnutrition]I Birlouez, M J Cals, G Covi, et al.
Annales De Biologie Clinique|July 31, 2002
[Vitamins and aging]I Birlouez, M J Cals, G Covi, et al.
Annales De Biologie Clinique|July 31, 2002
[Vitamins and biotechnologies]I Birlouez, M J Cals, G Covi, et al.
Annales De Biologie Clinique|April 3, 2001
[4th Symposium of the Francophone Society of Vitamins and Biological Factors. Dijon, France, 3-4 December 1999]I Birlouez, M J Cals, G Covi, et al.
Neurology|August 30, 2008
Second consensus statement on the diagnosis of multiple system atrophyS Gilman, G K Wenning, P A Low, et al.
Journal of Medical Genetics|October 18, 2005
Epsilon sarcoglycan mutations and phenotype in French patients with myoclonic syndromesS Tezenas du Montcel, F Clot, M Vidailhet, et al.
Neurology|March 26, 2008
Myoclonus-dystonia: clinical and electrophysiologic pattern related to SGCE mutationsE Roze, E Apartis, F Clot, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 1, 1996
[Sleeping position, prevention of sudden death syndrome and gastroesophageal reflux]C Faure, B Leluyer, Y Aujard, et al.
European Journal of Neurology|January 3, 2013
EFNS/MDS-ES/ENS [corrected] recommendations for the diagnosis of Parkinson's diseaseA Berardelli, G K Wenning, A Antonini, et al.
Scientific Reports|November 12, 2017
Comparing ataxias with oculomotor apraxia: a multimodal study of AOA1, AOA2 and AT focusing on video-oculography and alpha-fetoproteinL L Mariani, S Rivaud-Péchoux, P Charles, et al.
Pageof 31

Showing results (291-300 of 303) with videos related to

Sort By:
Pageof 31
Annales De Biologie Clinique|July 31, 2002
[Vitamin deficiency and malnutrition]I Birlouez, M J Cals, G Covi, et al.
Annales De Biologie Clinique|July 31, 2002
[Vitamins and aging]I Birlouez, M J Cals, G Covi, et al.
Annales De Biologie Clinique|July 31, 2002
[Vitamins and biotechnologies]I Birlouez, M J Cals, G Covi, et al.
Annales De Biologie Clinique|April 3, 2001
[4th Symposium of the Francophone Society of Vitamins and Biological Factors. Dijon, France, 3-4 December 1999]I Birlouez, M J Cals, G Covi, et al.
Neurology|August 30, 2008
Second consensus statement on the diagnosis of multiple system atrophyS Gilman, G K Wenning, P A Low, et al.
Journal of Medical Genetics|October 18, 2005
Epsilon sarcoglycan mutations and phenotype in French patients with myoclonic syndromesS Tezenas du Montcel, F Clot, M Vidailhet, et al.
Neurology|March 26, 2008
Myoclonus-dystonia: clinical and electrophysiologic pattern related to SGCE mutationsE Roze, E Apartis, F Clot, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 1, 1996
[Sleeping position, prevention of sudden death syndrome and gastroesophageal reflux]C Faure, B Leluyer, Y Aujard, et al.
European Journal of Neurology|January 3, 2013
EFNS/MDS-ES/ENS [corrected] recommendations for the diagnosis of Parkinson's diseaseA Berardelli, G K Wenning, A Antonini, et al.
Scientific Reports|November 12, 2017
Comparing ataxias with oculomotor apraxia: a multimodal study of AOA1, AOA2 and AT focusing on video-oculography and alpha-fetoproteinL L Mariani, S Rivaud-Péchoux, P Charles, et al.
Pageof 31