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F Labarthe

Showing results (21-30 of 37) with videos related to

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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 11, 2008
[Enzyme replacement therapy in a boy with infantile Pompe disease: cardiac follow-up]R Bonnefoy, F Labarthe, F Paoli, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 4, 2004
[Compliance to atopia preventive regimes after discharge from maternity services]C Hoarau, C Maurage, F Labarthe, et al.
Transplant Infectious Disease : an Official Journal of the Transplantation Society|December 5, 2013
Successful treatment with fumagillin of the first pediatric case of digestive microsporidiosis in a liver-kidney transplantG Desoubeaux, Z Maakaroun-Vermesse, C Lier, et al.
Journal Francais D'Ophtalmologie|December 25, 2008
[Long-chain 3-hydroxyacyl CoA dehydrogenase deficiency and choroidal neovascularization]D Stopek, E Gitteau Lala, F Labarthe, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 16, 2012
[Benefits of continuous subcutaneous insulin infusion in children with type 1 diabetes mellitus]C Hasselmann, E Bonnemaison, N Faure, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 7, 2014
[Donohue syndrome or leprechaunism]D Planchenault, D Martin-Coignard, D Rugemintwaza, et al.
Journal Francais D'Ophtalmologie|December 14, 2024
Homocystinuria in a 14-year-old girl with neurodevelopmental delayN Mureau, F Chapart, M Perivier, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 18, 2004
Adult onset ornithine transcarbamylase deficiency: an unusual cause of semantic disordersS Rimbaux, C Hommet, D Perrier, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 23, 2006
[Pathologic childhood aerophagia]N Delaperrière, M Orega, C Maurage, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|February 24, 2009
[Clinical variability and diagnosis steps in childhood mitochondrial disease]S Mercier, M Josselin de Wasch, F Labarthe, et al.
Pageof 4

Showing results (21-30 of 37) with videos related to

Sort By:
Pageof 4
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 11, 2008
[Enzyme replacement therapy in a boy with infantile Pompe disease: cardiac follow-up]R Bonnefoy, F Labarthe, F Paoli, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 4, 2004
[Compliance to atopia preventive regimes after discharge from maternity services]C Hoarau, C Maurage, F Labarthe, et al.
Transplant Infectious Disease : an Official Journal of the Transplantation Society|December 5, 2013
Successful treatment with fumagillin of the first pediatric case of digestive microsporidiosis in a liver-kidney transplantG Desoubeaux, Z Maakaroun-Vermesse, C Lier, et al.
Journal Francais D'Ophtalmologie|December 25, 2008
[Long-chain 3-hydroxyacyl CoA dehydrogenase deficiency and choroidal neovascularization]D Stopek, E Gitteau Lala, F Labarthe, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 16, 2012
[Benefits of continuous subcutaneous insulin infusion in children with type 1 diabetes mellitus]C Hasselmann, E Bonnemaison, N Faure, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 7, 2014
[Donohue syndrome or leprechaunism]D Planchenault, D Martin-Coignard, D Rugemintwaza, et al.
Journal Francais D'Ophtalmologie|December 14, 2024
Homocystinuria in a 14-year-old girl with neurodevelopmental delayN Mureau, F Chapart, M Perivier, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 18, 2004
Adult onset ornithine transcarbamylase deficiency: an unusual cause of semantic disordersS Rimbaux, C Hommet, D Perrier, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 23, 2006
[Pathologic childhood aerophagia]N Delaperrière, M Orega, C Maurage, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|February 24, 2009
[Clinical variability and diagnosis steps in childhood mitochondrial disease]S Mercier, M Josselin de Wasch, F Labarthe, et al.
Pageof 4