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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
June 17, 2008
[GLUT-1 deficiency syndrome or De Vivo disease: a case report]
I Ticus, A Cano, N Villeneuve, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
March 11, 2015
[Vitamin D deficiency rickets complicating Dorfman-Chanarin syndrome]
C Barraud, A Cano, C Boulay, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
July 14, 2012
[Neuromyelitis optica in children. Two case reports]
B Tosello, C Halbert, J Mancini, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
February 6, 2008
[Epileptic seizures in childhood: from seizure type to diagnosis]
M Milh, I Ticus, N Villeneuve, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
December 11, 2013
[Postinfectious family case of acute necrotizing encephalopathy caused by RANBP2 gene mutation]
C Di Meglio, A Cano, M Milh, et al.
Revue Neurologique
|
March 20, 2016
Severe neonatal seizures: From molecular diagnosis to precision therapy?
M Milh, P Cacciagli, C Ravix, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 21, 2005
Altering cannabinoid signaling during development disrupts neuronal activity
C Bernard, M Milh, Y M Morozov, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
April 23, 2010
[Language disorders in children with morphologic abnormalities of the hippocampus]
G Agostini, J Mancini, B Chabrol, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
December 21, 2020
The phenotype caused by recessive variations in SLC25A22: Report of a new case and literature review
M-V André, P Cacciagli, A Cano, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
January 1, 2015
Clinical presentation of PTEN mutations in childhood in the absence of family history of Cowden syndrome
T Busa, M Milh, N Degardin, et al.
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of 3
Search research articles
Search
Showing results (11-20 of 29) with videos related to
Sort By:
Page
of 3
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
June 17, 2008
[GLUT-1 deficiency syndrome or De Vivo disease: a case report]
I Ticus, A Cano, N Villeneuve, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
March 11, 2015
[Vitamin D deficiency rickets complicating Dorfman-Chanarin syndrome]
C Barraud, A Cano, C Boulay, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
July 14, 2012
[Neuromyelitis optica in children. Two case reports]
B Tosello, C Halbert, J Mancini, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
February 6, 2008
[Epileptic seizures in childhood: from seizure type to diagnosis]
M Milh, I Ticus, N Villeneuve, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
December 11, 2013
[Postinfectious family case of acute necrotizing encephalopathy caused by RANBP2 gene mutation]
C Di Meglio, A Cano, M Milh, et al.
Revue Neurologique
|
March 20, 2016
Severe neonatal seizures: From molecular diagnosis to precision therapy?
M Milh, P Cacciagli, C Ravix, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 21, 2005
Altering cannabinoid signaling during development disrupts neuronal activity
C Bernard, M Milh, Y M Morozov, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
April 23, 2010
[Language disorders in children with morphologic abnormalities of the hippocampus]
G Agostini, J Mancini, B Chabrol, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
December 21, 2020
The phenotype caused by recessive variations in SLC25A22: Report of a new case and literature review
M-V André, P Cacciagli, A Cano, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
January 1, 2015
Clinical presentation of PTEN mutations in childhood in the absence of family history of Cowden syndrome
T Busa, M Milh, N Degardin, et al.
Page
of 3