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Brigitte Chabrol

Showing results (21-30 of 147) with videos related to

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Clinical Chemistry|November 11, 2022
Hyperglycinemia in a 5-Week-Old Boy with Pulmonary Arterial HypertensionJulien Neveu, Aline Cano, Celia Hoebeke, et al.
Pediatrics|August 21, 2013
Diagnosis and outcome of SCN4A-related severe neonatal episodic laryngospasm (SNEL): 2 new casesEmilie Caietta, Mathieu Milh, Damien Sternberg, et al.
Clinical Nuclear Medicine|December 19, 2008
Multiple distal pulmonary arterial thromboses revealed by lung scintigraphy in a patient with homocystinuria and normal multidetector CT pulmonary angiographyLaurent Tessonnier, Eric Guedj, Aline Cano, et al.
Health and Quality of Life Outcomes|September 21, 2013
Assessment of quality of life of the children and parents affected by inborn errors of metabolism with restricted diet: preliminary results of a cross-sectional studyAlexandre Fabre, Karine Baumstarck, Aline Cano, et al.
Epilepsy & Behavior : E&B|January 14, 2014
Cognitive and adaptive evaluation of 21 consecutive patients with Dravet syndromeNathalie Villeneuve, Virginie Laguitton, Marine Viellard, et al.
Pediatric Research|August 1, 2002
Magnetic resonance spectroscopy study of glycine pathways in nonketotic hyperglycinemiaAngèle Viola, Brigitte Chabrol, François Nicoli, et al.
Molecular Genetics and Metabolism|May 23, 2017
Assembly defects of multiple respiratory chain complexes in a child with cardiac hypertrophy associated with a novel ACAD9 mutationKonstantina Fragaki, Annabelle Chaussenot, Audrey Boutron, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 17, 2017
Heterogeneity of FHF1 related phenotype: Novel case with early onset severe attacks of apnea, partial mitochondrial respiratory chain complex II deficiency, neonatal onset seizures without neurodegenerationNathalie Villeneuve, Affef Abidi, Pierre Cacciagli, et al.
Brain & Development|November 7, 2015
Cerebral (18)FluoroDeoxy-Glucose Positron Emission Tomography in paediatric anti N-methyl-D-aspartate receptor encephalitis: A case seriesStanislas Lagarde, Anne Lepine, Emilie Caietta, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 21, 2020
Cerliponase alfa changes the natural history of children with neuronal ceroid lipofuscinosis type 2: The first French cohortBastien Estublier, Aline Cano, Célia Hoebeke, et al.
Pageof 15

Showing results (21-30 of 147) with videos related to

Sort By:
Pageof 15
Clinical Chemistry|November 11, 2022
Hyperglycinemia in a 5-Week-Old Boy with Pulmonary Arterial HypertensionJulien Neveu, Aline Cano, Celia Hoebeke, et al.
Pediatrics|August 21, 2013
Diagnosis and outcome of SCN4A-related severe neonatal episodic laryngospasm (SNEL): 2 new casesEmilie Caietta, Mathieu Milh, Damien Sternberg, et al.
Clinical Nuclear Medicine|December 19, 2008
Multiple distal pulmonary arterial thromboses revealed by lung scintigraphy in a patient with homocystinuria and normal multidetector CT pulmonary angiographyLaurent Tessonnier, Eric Guedj, Aline Cano, et al.
Health and Quality of Life Outcomes|September 21, 2013
Assessment of quality of life of the children and parents affected by inborn errors of metabolism with restricted diet: preliminary results of a cross-sectional studyAlexandre Fabre, Karine Baumstarck, Aline Cano, et al.
Epilepsy & Behavior : E&B|January 14, 2014
Cognitive and adaptive evaluation of 21 consecutive patients with Dravet syndromeNathalie Villeneuve, Virginie Laguitton, Marine Viellard, et al.
Pediatric Research|August 1, 2002
Magnetic resonance spectroscopy study of glycine pathways in nonketotic hyperglycinemiaAngèle Viola, Brigitte Chabrol, François Nicoli, et al.
Molecular Genetics and Metabolism|May 23, 2017
Assembly defects of multiple respiratory chain complexes in a child with cardiac hypertrophy associated with a novel ACAD9 mutationKonstantina Fragaki, Annabelle Chaussenot, Audrey Boutron, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 17, 2017
Heterogeneity of FHF1 related phenotype: Novel case with early onset severe attacks of apnea, partial mitochondrial respiratory chain complex II deficiency, neonatal onset seizures without neurodegenerationNathalie Villeneuve, Affef Abidi, Pierre Cacciagli, et al.
Brain & Development|November 7, 2015
Cerebral (18)FluoroDeoxy-Glucose Positron Emission Tomography in paediatric anti N-methyl-D-aspartate receptor encephalitis: A case seriesStanislas Lagarde, Anne Lepine, Emilie Caietta, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 21, 2020
Cerliponase alfa changes the natural history of children with neuronal ceroid lipofuscinosis type 2: The first French cohortBastien Estublier, Aline Cano, Célia Hoebeke, et al.
Pageof 15