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Isabelle Caubel

Showing results (1-10 of 9) with videos related to

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Presse Medicale (Paris, France : 1983)|May 8, 2003
[Epidemiologic, clinical, biological and therapeutic aspects of Gaucher disease]Jérôme Stirnemann, Isabelle Caubel, Adrien Kettaneh, et al.
Journal De La Societe De Biologie|October 4, 2002
[Gaucher's disease ]Nadia Belmatoug, Isabelle Caubel, Jérôme Stirnemann, et al.
Bulletin De L'Academie Nationale De Medecine|November 5, 2002
[French results of enzyme replacement therapy in Gaucher's disease]Gérard Schaison, Isabelle Caubel, Nadia Belmatoug, et al.
Epilepsy Research|May 13, 2008
Combination of infantile spasms, non-epileptic seizures and complex movement disorder: a new case of ARX-related epilepsyKarine Poirier, Monika Eisermann, Isabelle Caubel, et al.
Frontiers in Pediatrics|March 22, 2021
West Syndrome Is an Exceptional Presentation of Pyridoxine- and Pyridoxal Phosphate-Dependent Epilepsy: Data From a French Cohort and Review of the LiteratureMarc Gibaud, Magalie Barth, Jérémie Lefranc, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 27, 2012
Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the TITF1/NKX2-1 geneDomitille Gras, Laurence Jonard, Emmanuel Roze, et al.
Epilepsia|April 3, 2016
Epilepsy diagnostic and treatment needs identified with a collaborative database involving tertiary centers in FranceMathilde Chipaux, William Szurhaj, Laurent Vercueil, et al.
Neurology. Genetics|December 12, 2018
Delineating <i>FOXG1</i> syndrome: From congenital microcephaly to hyperkinetic encephalopathyNancy Vegas, Mara Cavallin, Camille Maillard, et al.
Neurology|May 26, 2026
Burst-Suppression EEG in Early Infantile Developmental and Epileptic Encephalopathies: Phenotype, Genotype, and OutcomeFlorence Riccardi, Béatrice Desnous, Emilie Borloz, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Presse Medicale (Paris, France : 1983)|May 8, 2003
[Epidemiologic, clinical, biological and therapeutic aspects of Gaucher disease]Jérôme Stirnemann, Isabelle Caubel, Adrien Kettaneh, et al.
Journal De La Societe De Biologie|October 4, 2002
[Gaucher's disease ]Nadia Belmatoug, Isabelle Caubel, Jérôme Stirnemann, et al.
Bulletin De L'Academie Nationale De Medecine|November 5, 2002
[French results of enzyme replacement therapy in Gaucher's disease]Gérard Schaison, Isabelle Caubel, Nadia Belmatoug, et al.
Epilepsy Research|May 13, 2008
Combination of infantile spasms, non-epileptic seizures and complex movement disorder: a new case of ARX-related epilepsyKarine Poirier, Monika Eisermann, Isabelle Caubel, et al.
Frontiers in Pediatrics|March 22, 2021
West Syndrome Is an Exceptional Presentation of Pyridoxine- and Pyridoxal Phosphate-Dependent Epilepsy: Data From a French Cohort and Review of the LiteratureMarc Gibaud, Magalie Barth, Jérémie Lefranc, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 27, 2012
Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the TITF1/NKX2-1 geneDomitille Gras, Laurence Jonard, Emmanuel Roze, et al.
Epilepsia|April 3, 2016
Epilepsy diagnostic and treatment needs identified with a collaborative database involving tertiary centers in FranceMathilde Chipaux, William Szurhaj, Laurent Vercueil, et al.
Neurology. Genetics|December 12, 2018
Delineating <i>FOXG1</i> syndrome: From congenital microcephaly to hyperkinetic encephalopathyNancy Vegas, Mara Cavallin, Camille Maillard, et al.
Neurology|May 26, 2026
Burst-Suppression EEG in Early Infantile Developmental and Epileptic Encephalopathies: Phenotype, Genotype, and OutcomeFlorence Riccardi, Béatrice Desnous, Emilie Borloz, et al.
Pageof 1