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V Des Portes

Showing results (21-30 of 59) with videos related to

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Neuropediatrics|August 12, 2003
Familial bilateral medial parietooccipital band heterotopia not related to DCX or LIS1 gene defectsN Deconinck, T Duprez, V des Portes, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 21, 2012
[Diagnosis and care of Wilson disease with neurological revelation]S Wagner, A-S Brunet, M Bost, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 25, 2007
[Acute hemiparesis revealing a neuroborreliosis in a child]C Rénard, S Marignier, Y Gillet, et al.
Annales De Genetique|May 26, 1998
A gene for non-specific X-linked mental retardation (MRX55) is located in Xp11S C Deqaqi, M N'Guessan, J Forner, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 3, 2014
[Type 2 neurofibromatosis: intergenerational differences in genetic and clinical expression]A Drouet, F Le Moigne, D Salamé, et al.
American Journal of Medical Genetics|May 8, 2000
X-linked congenital ataxia: a clinical and genetic studyE Bertini, V des Portes, G Zanni, et al.
American Journal of Medical Genetics|July 9, 1999
Refined 2.7 centimorgan locus in Xp21.3-22.1 for a nonspecific X-linked mental retardation gene (MRX54)L B Jemaa, V des Portes, R Zemni, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|June 24, 2008
Abnormal Sylvian fissure on prenatal cerebral imaging: significance and correlation with neuropathological and postnatal dataL Guibaud, L Selleret, J C Larroche, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|June 13, 2012
Prenatal diagnosis of cerebellar cortical dysplasia associated with abnormalities of foliationM Massoud, J Clerc, M Cagneux, et al.
Seizure|May 25, 2002
So-called 'cryptogenic' partial seizures resulting from a subtle cortical dysgenesis due to a doublecortin gene mutationV des Portes, L Abaoub, A Joannard, et al.
Pageof 6

Showing results (21-30 of 59) with videos related to

Sort By:
Pageof 6
Neuropediatrics|August 12, 2003
Familial bilateral medial parietooccipital band heterotopia not related to DCX or LIS1 gene defectsN Deconinck, T Duprez, V des Portes, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 21, 2012
[Diagnosis and care of Wilson disease with neurological revelation]S Wagner, A-S Brunet, M Bost, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 25, 2007
[Acute hemiparesis revealing a neuroborreliosis in a child]C Rénard, S Marignier, Y Gillet, et al.
Annales De Genetique|May 26, 1998
A gene for non-specific X-linked mental retardation (MRX55) is located in Xp11S C Deqaqi, M N'Guessan, J Forner, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 3, 2014
[Type 2 neurofibromatosis: intergenerational differences in genetic and clinical expression]A Drouet, F Le Moigne, D Salamé, et al.
American Journal of Medical Genetics|May 8, 2000
X-linked congenital ataxia: a clinical and genetic studyE Bertini, V des Portes, G Zanni, et al.
American Journal of Medical Genetics|July 9, 1999
Refined 2.7 centimorgan locus in Xp21.3-22.1 for a nonspecific X-linked mental retardation gene (MRX54)L B Jemaa, V des Portes, R Zemni, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|June 24, 2008
Abnormal Sylvian fissure on prenatal cerebral imaging: significance and correlation with neuropathological and postnatal dataL Guibaud, L Selleret, J C Larroche, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|June 13, 2012
Prenatal diagnosis of cerebellar cortical dysplasia associated with abnormalities of foliationM Massoud, J Clerc, M Cagneux, et al.
Seizure|May 25, 2002
So-called 'cryptogenic' partial seizures resulting from a subtle cortical dysgenesis due to a doublecortin gene mutationV des Portes, L Abaoub, A Joannard, et al.
Pageof 6