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Epilepsia
|
December 1, 1995
Absence epilepsies
P Loiseau, B Duché, J M Pédespan
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
October 16, 2012
[Neurological manifestations of an osteoid osteoma located on the femoral neck in an 8-year-old boy]
S Cabasson, M Yvert, P Pillet, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
December 20, 2014
[Gradenigo syndrome and petrositis in a child]
M Favier, P Bessou, V Franco-Vidal, et al.
The British Journal of Radiology
|
March 3, 2001
MRI and clinical differences between optic pathway tumours in children with and without neurofibromatosis
J F Chateil, C Soussotte, J M Pédespan, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
March 15, 2011
[Polymorphic expression of epilepsy and cognitive impairment in ring chromosome 20 syndrome]
F Villéga, H Ngayap, C Espil-Taris, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
April 6, 2005
[Angelman syndrome and intracranial aneurysm: fortuitous association or commune genetic predisposition?]
S Meyer Witte, C Espil-Taris, C Cenraud, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 6) with videos related to
Sort By:
Page
of 1
Epilepsia
|
December 1, 1995
Absence epilepsies
P Loiseau, B Duché, J M Pédespan
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
October 16, 2012
[Neurological manifestations of an osteoid osteoma located on the femoral neck in an 8-year-old boy]
S Cabasson, M Yvert, P Pillet, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
December 20, 2014
[Gradenigo syndrome and petrositis in a child]
M Favier, P Bessou, V Franco-Vidal, et al.
The British Journal of Radiology
|
March 3, 2001
MRI and clinical differences between optic pathway tumours in children with and without neurofibromatosis
J F Chateil, C Soussotte, J M Pédespan, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
March 15, 2011
[Polymorphic expression of epilepsy and cognitive impairment in ring chromosome 20 syndrome]
F Villéga, H Ngayap, C Espil-Taris, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
April 6, 2005
[Angelman syndrome and intracranial aneurysm: fortuitous association or commune genetic predisposition?]
S Meyer Witte, C Espil-Taris, C Cenraud, et al.
Page
of 1