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C Barnerias

Showing results (1-10 of 15) with videos related to

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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 28, 2020
Spinal muscular atrophy (SMA) type I (Werdnig-Hoffmann disease)F Audic, C Barnerias
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 31, 2006
[Afebrile seizures in gastroenteritis: a Japanese peculiarity]C Chalouhi, C Barnerias, V Abadie
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 28, 2020
Clinical features of spinal muscular atrophy (SMA) type 2C Cancès, C Richelme, C Barnerias, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 28, 2020
Multidisciplinary approach and psychosocial management of spinal muscular atrophy (SMA)J Ropars, S Peudenier, A Genot, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 15, 2004
[Central nervous system tumor: an unusual etiology for limb pain]W Gueddari, D Garel, C Barnerias, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 16, 2007
[Management of neonatal seizures]A Kaminska, J Mourdie, C Barnerias, et al.
Journal of Inherited Metabolic Disease|September 20, 2007
Peripheral neuropathy and inborn errors of metabolism in adultsF Sedel, C Barnerias, O Dubourg, et al.
Journal Francais D'Ophtalmologie|May 9, 2024
[Pediatric myasthenia with ocular involvement]L Prud'homme, C Gitiaux, C Barnerias, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 21, 2023
Correlations between clinical motor scores and CMAP in patients with type 2 spinal muscular amyotrophy treated with nusinersenM Richard, R Barrois, I Desguerre, et al.
European Journal of Medical Genetics|October 8, 2013
A novel mutation in STXBP1 causing epileptic encephalopathy (late onset infantile spasms) with partial respiratory chain complex IV deficiencyG Barcia, C Barnerias, M Rio, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 28, 2020
Spinal muscular atrophy (SMA) type I (Werdnig-Hoffmann disease)F Audic, C Barnerias
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 31, 2006
[Afebrile seizures in gastroenteritis: a Japanese peculiarity]C Chalouhi, C Barnerias, V Abadie
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 28, 2020
Clinical features of spinal muscular atrophy (SMA) type 2C Cancès, C Richelme, C Barnerias, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 28, 2020
Multidisciplinary approach and psychosocial management of spinal muscular atrophy (SMA)J Ropars, S Peudenier, A Genot, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 15, 2004
[Central nervous system tumor: an unusual etiology for limb pain]W Gueddari, D Garel, C Barnerias, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 16, 2007
[Management of neonatal seizures]A Kaminska, J Mourdie, C Barnerias, et al.
Journal of Inherited Metabolic Disease|September 20, 2007
Peripheral neuropathy and inborn errors of metabolism in adultsF Sedel, C Barnerias, O Dubourg, et al.
Journal Francais D'Ophtalmologie|May 9, 2024
[Pediatric myasthenia with ocular involvement]L Prud'homme, C Gitiaux, C Barnerias, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 21, 2023
Correlations between clinical motor scores and CMAP in patients with type 2 spinal muscular amyotrophy treated with nusinersenM Richard, R Barrois, I Desguerre, et al.
European Journal of Medical Genetics|October 8, 2013
A novel mutation in STXBP1 causing epileptic encephalopathy (late onset infantile spasms) with partial respiratory chain complex IV deficiencyG Barcia, C Barnerias, M Rio, et al.
Pageof 2