Search research articles
Contact Us
Filters
Showing results (21-30 of 44) with videos related to
Page
of 5
Sort By:
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
May 17, 2021
Clinical characteristics of COVID-19 infection in polyhandicapped persons in France
M-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 syndrome
A 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 review
H 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 human
F 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-serine
A Brassier, V Valayannopoulos, N Bahi-Buisson, et al.
Neuropediatrics
|
March 17, 2006
Molar tooth sign and superior vermian dysplasia: a radiological, clinical, and genetic study
S 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 encephalopathy
H 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 Ia
J 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 deficiency
M Barth, V Serre, L Hubert, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 44) with videos related to
Sort By:
Page
of 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 France
M-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 syndrome
A 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 review
H 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 human
F 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-serine
A Brassier, V Valayannopoulos, N Bahi-Buisson, et al.
Neuropediatrics
|
March 17, 2006
Molar tooth sign and superior vermian dysplasia: a radiological, clinical, and genetic study
S 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 encephalopathy
H 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 Ia
J 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 deficiency
M Barth, V Serre, L Hubert, et al.
Page
of 5