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V Des Portes

Showing results (11-20 of 59) with videos related to

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Neuroreport|October 3, 1994
Early detection of mouse wobbler mutation: a model of pathological motoneurone deathV des Portes, M Coulpier, J Melki, et al.
Journal of Intellectual Disability Research : JIDR|March 23, 2011
Implicit procedural learning in fragile X and Down syndromeG Bussy, E Charrin, A Brun, et al.
Revue Neurologique|April 1, 2005
[Creatine deficiency syndromes]D Cheillan, S Cognat, N Vandenberghe, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|October 29, 2005
Extracerebellar ectopic brain tissue in the posterior fossaL Guibaud, S Devonec, V Des Portes, et al.
Neuropediatrics|December 19, 2009
Neurological outcome and risk of recurrence depending on the anterior vs. posterior arterial distribution in children with strokeA Touré, S Chabrier, M D Plagne, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 25, 2000
[Mental retardation and disorders of cortical development]V Des Portes, J M Pinard, F Francis, et al.
Developmental Medicine and Child Neurology|September 25, 2008
'Absence of T378N mutation of ATP1A2 gene in five patients with alternating hemiplegia of childhood'S Boileau, I Vuillaume, B Sablonnière, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|May 13, 2008
Prenatal cerebral ultrasound and MRI findings in glutaric aciduria Type 1: a de novo caseC Mellerio, S Marignier, P Roth, et al.
Neurology|July 23, 2003
Herpes simplex encephalitis relapses in children: differentiation of two neurologic entitiesX De Tiège, F Rozenberg, V Des Portes, et al.
European Journal of Medical Genetics|October 10, 2022
STAG2 microduplication in a patient with eyelid myoclonia and absences and a review of EMA-related reported genesZ Gokce-Samar, J de Bellescize, A Arzimanoglou, et al.
Pageof 6

Showing results (11-20 of 59) with videos related to

Sort By:
Pageof 6
Neuroreport|October 3, 1994
Early detection of mouse wobbler mutation: a model of pathological motoneurone deathV des Portes, M Coulpier, J Melki, et al.
Journal of Intellectual Disability Research : JIDR|March 23, 2011
Implicit procedural learning in fragile X and Down syndromeG Bussy, E Charrin, A Brun, et al.
Revue Neurologique|April 1, 2005
[Creatine deficiency syndromes]D Cheillan, S Cognat, N Vandenberghe, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|October 29, 2005
Extracerebellar ectopic brain tissue in the posterior fossaL Guibaud, S Devonec, V Des Portes, et al.
Neuropediatrics|December 19, 2009
Neurological outcome and risk of recurrence depending on the anterior vs. posterior arterial distribution in children with strokeA Touré, S Chabrier, M D Plagne, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 25, 2000
[Mental retardation and disorders of cortical development]V Des Portes, J M Pinard, F Francis, et al.
Developmental Medicine and Child Neurology|September 25, 2008
'Absence of T378N mutation of ATP1A2 gene in five patients with alternating hemiplegia of childhood'S Boileau, I Vuillaume, B Sablonnière, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|May 13, 2008
Prenatal cerebral ultrasound and MRI findings in glutaric aciduria Type 1: a de novo caseC Mellerio, S Marignier, P Roth, et al.
Neurology|July 23, 2003
Herpes simplex encephalitis relapses in children: differentiation of two neurologic entitiesX De Tiège, F Rozenberg, V Des Portes, et al.
European Journal of Medical Genetics|October 10, 2022
STAG2 microduplication in a patient with eyelid myoclonia and absences and a review of EMA-related reported genesZ Gokce-Samar, J de Bellescize, A Arzimanoglou, et al.
Pageof 6