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A Roubertie

Showing results (21-30 of 49) with videos related to

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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 intoleranceV 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 patientsL-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 reportsP 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.
Pageof 5

Showing results (21-30 of 49) with videos related to

Sort By:
Pageof 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 intoleranceV 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 patientsL-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 reportsP 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.
Pageof 5