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Journal of Child Neurology
|
August 21, 2001
Is hyperprolinemia type I actually a benign trait? Report of a case with severe neurologic involvement and vigabatrin intolerance
V Humbertclaude, F Rivier, A Roubertie, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
May 13, 2006
[Movement disorders in children]
A Roubertie, S Thobois, A de Saint Martin, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
November 14, 2003
[Movement disorders in childhood: classification and genetic update]
A Roubertie, F Rivier, S Tuffery-Giraud, et al.
Annales De Dermatologie Et De Venereologie
|
May 8, 2022
Dermatological and genetic data in tuberous sclerosis: A prospective single-center study of 38 patients
L-P Secco, C Coubes, P Meyer, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
September 21, 2010
[Acute inflammatory polyradiculoneuropathy and membranous glomerulonephritis following Epbstein-Barr virus primary infection in a 12-year-old girl]
P Meyer, S Soëte, P Raynaud, et al.
Revue Neurologique
|
May 2, 2002
[The varied etiologies of childhood-onset dystonia]
A Roubertie, F Rivier, V Humbertclaude, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
March 29, 2001
[Acute myelitis of an unusual cause in a child: the lymphocytic choriomeningitis virus]
V Humbertclaude, S Tourtet, M Semprino, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
July 19, 2011
[Neonatal seizures management]
A Roubertie, F Masson, A de Villepin-Touzery, et al.
Brain & Development
|
January 12, 2010
Unexpected neurological sequelae following propofol anesthesia in infants: Three case reports
P Meyer, C Langlois, S Soëte, et al.
Brain & Development
|
November 27, 2001
Neurological presentation of three patients with 22q11 deletion (CATCH 22 syndrome)
A Roubertie, M Semprino, A M Chaze, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 49) with videos related to
Sort By:
Page
of 5
Journal of Child Neurology
|
August 21, 2001
Is hyperprolinemia type I actually a benign trait? Report of a case with severe neurologic involvement and vigabatrin intolerance
V Humbertclaude, F Rivier, A Roubertie, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
May 13, 2006
[Movement disorders in children]
A Roubertie, S Thobois, A de Saint Martin, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
November 14, 2003
[Movement disorders in childhood: classification and genetic update]
A Roubertie, F Rivier, S Tuffery-Giraud, et al.
Annales De Dermatologie Et De Venereologie
|
May 8, 2022
Dermatological and genetic data in tuberous sclerosis: A prospective single-center study of 38 patients
L-P Secco, C Coubes, P Meyer, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
September 21, 2010
[Acute inflammatory polyradiculoneuropathy and membranous glomerulonephritis following Epbstein-Barr virus primary infection in a 12-year-old girl]
P Meyer, S Soëte, P Raynaud, et al.
Revue Neurologique
|
May 2, 2002
[The varied etiologies of childhood-onset dystonia]
A Roubertie, F Rivier, V Humbertclaude, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
March 29, 2001
[Acute myelitis of an unusual cause in a child: the lymphocytic choriomeningitis virus]
V Humbertclaude, S Tourtet, M Semprino, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
July 19, 2011
[Neonatal seizures management]
A Roubertie, F Masson, A de Villepin-Touzery, et al.
Brain & Development
|
January 12, 2010
Unexpected neurological sequelae following propofol anesthesia in infants: Three case reports
P Meyer, C Langlois, S Soëte, et al.
Brain & Development
|
November 27, 2001
Neurological presentation of three patients with 22q11 deletion (CATCH 22 syndrome)
A Roubertie, M Semprino, A M Chaze, et al.
Page
of 5