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M Vidailhet

Showing results (211-220 of 303) with videos related to

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Annals of Neurology|April 1, 1994
Eye movements in parkinsonian syndromesM Vidailhet, S Rivaud, N Gouider-Khouja, et al.
Journal of Clinical Microbiology|October 1, 1993
Arbitrarily primed polymerase chain reaction as a rapid method to differentiate crossed from independent Pseudomonas cepacia infections in cystic fibrosis patientsE H Bingen, M Weber, J Derelle, et al.
Neurology|July 25, 2007
Structural abnormalities in the cerebellum and sensorimotor circuit in writer's crampC Delmaire, M Vidailhet, A Elbaz, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 1, 1996
[Pregnancy and the child of a mother with phenylketonuria]V Abadie, E Depondt, J P Farriaux, et al.
Annales De Pathologie|January 1, 1986
[Hyalinosis cutis and mucosae. Ultrastructural histochemical aspects indicating intracellular accumulation of glycosaminoglycans]B P Leheup, C Jeandel, J C Guedenet, et al.
Neurology|September 1, 1993
The Bereitschaftspotential preceding simple foot movement and initiation of gait in Parkinson's diseaseM Vidailhet, F Stocchi, J C Rothwell, et al.
Neurology|December 1, 1994
Isolated motor control dysfunction related to progressive multifocal leukoencephalopathy during AIDS with normal MRIB de Toffol, M Vidailhet, F Gray, et al.
Intensive Care Medicine|August 5, 2003
Adult presentation of MCAD deficiency revealed by coma and severe arrythmiasF Feillet, G Steinmann, C Vianey-Saban, et al.
Revue Neurologique|July 21, 2009
Familial cortical myoclonic tremor with epilepsy (FCMTE): Clinical characteristics and exclusion of linkages to 8q and 2p in a large French familyE Magnin, M Vidailhet, C Depienne, et al.
Archives of Biochemistry and Biophysics|October 24, 1998
Two missense point mutations in different alleles in the 3-hydroxy-3-methylglutaryl coenzyme A lyase gene produce 3-hydroxy-3-methylglutaric aciduria in a French patientN Zapater, J Pié, J Lloberas, et al.
Pageof 31

Showing results (211-220 of 303) with videos related to

Sort By:
Pageof 31
Annals of Neurology|April 1, 1994
Eye movements in parkinsonian syndromesM Vidailhet, S Rivaud, N Gouider-Khouja, et al.
Journal of Clinical Microbiology|October 1, 1993
Arbitrarily primed polymerase chain reaction as a rapid method to differentiate crossed from independent Pseudomonas cepacia infections in cystic fibrosis patientsE H Bingen, M Weber, J Derelle, et al.
Neurology|July 25, 2007
Structural abnormalities in the cerebellum and sensorimotor circuit in writer's crampC Delmaire, M Vidailhet, A Elbaz, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 1, 1996
[Pregnancy and the child of a mother with phenylketonuria]V Abadie, E Depondt, J P Farriaux, et al.
Annales De Pathologie|January 1, 1986
[Hyalinosis cutis and mucosae. Ultrastructural histochemical aspects indicating intracellular accumulation of glycosaminoglycans]B P Leheup, C Jeandel, J C Guedenet, et al.
Neurology|September 1, 1993
The Bereitschaftspotential preceding simple foot movement and initiation of gait in Parkinson's diseaseM Vidailhet, F Stocchi, J C Rothwell, et al.
Neurology|December 1, 1994
Isolated motor control dysfunction related to progressive multifocal leukoencephalopathy during AIDS with normal MRIB de Toffol, M Vidailhet, F Gray, et al.
Intensive Care Medicine|August 5, 2003
Adult presentation of MCAD deficiency revealed by coma and severe arrythmiasF Feillet, G Steinmann, C Vianey-Saban, et al.
Revue Neurologique|July 21, 2009
Familial cortical myoclonic tremor with epilepsy (FCMTE): Clinical characteristics and exclusion of linkages to 8q and 2p in a large French familyE Magnin, M Vidailhet, C Depienne, et al.
Archives of Biochemistry and Biophysics|October 24, 1998
Two missense point mutations in different alleles in the 3-hydroxy-3-methylglutaryl coenzyme A lyase gene produce 3-hydroxy-3-methylglutaric aciduria in a French patientN Zapater, J Pié, J Lloberas, et al.
Pageof 31