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N Bahi-Buisson

Showing results (21-30 of 44) with videos related to

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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 17, 2021
Clinical characteristics of COVID-19 infection in polyhandicapped persons in FranceM-C Rousseau, M Hully, M Milh, et al.
Revue Neurologique|September 24, 2008
[Epileptogenic brain malformations: radiological and clinical presentation and indications for genetic testing]N Bahi-Buisson, N Boddaert, Y Saillour, et al.
Journal of Medical Genetics|November 17, 2009
Updating the profile of C-terminal MECP2 deletions in Rett syndromeA Bebbington, A Percy, J Christodoulou, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|August 17, 2020
Heterogeneity in defining fetal corpus callosal pathology: systematic reviewH Mahallati, A Sotiriadis, C Celestin, et al.
Neuromuscular Disorders : NMD|March 31, 2015
A critical and previously unsuspected role for doublecortin at the neuromuscular junction in mouse and humanF Bourgeois, J Messéant, E Kordeli, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 28, 2015
Two new cases of serine deficiency disorders treated with l-serineA Brassier, V Valayannopoulos, N Bahi-Buisson, et al.
Neuropediatrics|March 17, 2006
Molar tooth sign and superior vermian dysplasia: a radiological, clinical, and genetic studyS Romano, N Boddaert, I Desguerre, et al.
Journal of Medical Genetics|November 13, 2007
Impairment of CDKL5 nuclear localisation as a cause for severe infantile encephalopathyH Rosas-Vargas, N Bahi-Buisson, C Philippe, et al.
Molecular Genetics and Metabolism|December 21, 2007
Risk assessment of acute vascular events in congenital disorder of glycosylation type IaJ B Arnoux, N Boddaert, V Valayannopoulos, et al.
JIMD Reports|February 23, 2013
Kinetic analyses guide the therapeutic decision in a novel form of moderate aromatic Acid decarboxylase deficiencyM Barth, V Serre, L Hubert, et al.
Pageof 5

Showing results (21-30 of 44) with videos related to

Sort By:
Pageof 5
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 17, 2021
Clinical characteristics of COVID-19 infection in polyhandicapped persons in FranceM-C Rousseau, M Hully, M Milh, et al.
Revue Neurologique|September 24, 2008
[Epileptogenic brain malformations: radiological and clinical presentation and indications for genetic testing]N Bahi-Buisson, N Boddaert, Y Saillour, et al.
Journal of Medical Genetics|November 17, 2009
Updating the profile of C-terminal MECP2 deletions in Rett syndromeA Bebbington, A Percy, J Christodoulou, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|August 17, 2020
Heterogeneity in defining fetal corpus callosal pathology: systematic reviewH Mahallati, A Sotiriadis, C Celestin, et al.
Neuromuscular Disorders : NMD|March 31, 2015
A critical and previously unsuspected role for doublecortin at the neuromuscular junction in mouse and humanF Bourgeois, J Messéant, E Kordeli, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 28, 2015
Two new cases of serine deficiency disorders treated with l-serineA Brassier, V Valayannopoulos, N Bahi-Buisson, et al.
Neuropediatrics|March 17, 2006
Molar tooth sign and superior vermian dysplasia: a radiological, clinical, and genetic studyS Romano, N Boddaert, I Desguerre, et al.
Journal of Medical Genetics|November 13, 2007
Impairment of CDKL5 nuclear localisation as a cause for severe infantile encephalopathyH Rosas-Vargas, N Bahi-Buisson, C Philippe, et al.
Molecular Genetics and Metabolism|December 21, 2007
Risk assessment of acute vascular events in congenital disorder of glycosylation type IaJ B Arnoux, N Boddaert, V Valayannopoulos, et al.
JIMD Reports|February 23, 2013
Kinetic analyses guide the therapeutic decision in a novel form of moderate aromatic Acid decarboxylase deficiencyM Barth, V Serre, L Hubert, et al.
Pageof 5