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Guy Touati

Showing results (31-40 of 49) with videos related to

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Journal of Hepatology|May 7, 2016
Severe respiratory complex III defect prevents liver adaptation to prolonged fastingLaura S Kremer, Caroline L'hermitte-Stead, Pierre Lesimple, et al.
Molecular Genetics and Metabolism|February 14, 2018
Long-term liver disease in methylmalonic and propionic acidemiasApolline Imbard, Nuria Garcia Segarra, Marine Tardieu, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 1, 2008
Spectrum of movement disorders associated with glutaric aciduria type 1: a study of 16 patientsCyril Gitiaux, Emmanuel Roze, Kiyoka Kinugawa, et al.
Annales D'Endocrinologie|May 4, 2004
Hyperinsulinemic hypoglycemia in childrenP de Lonlay, Irina Giurgea, Jean-Jacques Robert, et al.
The Journal of Clinical Endocrinology and Metabolism|February 7, 2004
Acute insulin responses to calcium and tolbutamide do not differentiate focal from diffuse congenital hyperinsulinismIrina Giurgea, Kathleen Laborde, Guy Touati, et al.
Journal of Inherited Metabolic Disease|March 4, 2017
Mitochondrial acetoacetyl-CoA thiolase deficiency: basal ganglia impairment may occur independently of ketoacidosisStéphanie Paquay, Agnès Bourillon, Samia Pichard, et al.
European Journal of Neurology|October 6, 2022
Movement disorders in valine métabolism diseases caused by HIBCH and ECHS1 deficienciesMarie-Céline François-Heude, Elise Lebigot, Emmanuel Roze, et al.
European Journal of Pediatrics|January 26, 2002
Heterogeneity of persistent hyperinsulinaemic hypoglycaemia. A series of 175 casesPascale de Lonlay, Jean-Christophe Fournet, Guy Touati, et al.
Orphanet Journal of Rare Diseases|March 16, 2019
Betaine anhydrous in homocystinuria: results from the RoCH registryVassili Valayannopoulos, Manuel Schiff, Nathalie Guffon, et al.
Molecular Genetics and Metabolism Reports|January 21, 2021
Enteral tube feeding in patients receiving dietary treatment for metabolic diseases: A retrospective analysis in a large French cohortClaire-Marine Bérat, Célina Roda, Anais Brassier, et al.
Pageof 5

Showing results (31-40 of 49) with videos related to

Sort By:
Pageof 5
Journal of Hepatology|May 7, 2016
Severe respiratory complex III defect prevents liver adaptation to prolonged fastingLaura S Kremer, Caroline L'hermitte-Stead, Pierre Lesimple, et al.
Molecular Genetics and Metabolism|February 14, 2018
Long-term liver disease in methylmalonic and propionic acidemiasApolline Imbard, Nuria Garcia Segarra, Marine Tardieu, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 1, 2008
Spectrum of movement disorders associated with glutaric aciduria type 1: a study of 16 patientsCyril Gitiaux, Emmanuel Roze, Kiyoka Kinugawa, et al.
Annales D'Endocrinologie|May 4, 2004
Hyperinsulinemic hypoglycemia in childrenP de Lonlay, Irina Giurgea, Jean-Jacques Robert, et al.
The Journal of Clinical Endocrinology and Metabolism|February 7, 2004
Acute insulin responses to calcium and tolbutamide do not differentiate focal from diffuse congenital hyperinsulinismIrina Giurgea, Kathleen Laborde, Guy Touati, et al.
Journal of Inherited Metabolic Disease|March 4, 2017
Mitochondrial acetoacetyl-CoA thiolase deficiency: basal ganglia impairment may occur independently of ketoacidosisStéphanie Paquay, Agnès Bourillon, Samia Pichard, et al.
European Journal of Neurology|October 6, 2022
Movement disorders in valine métabolism diseases caused by HIBCH and ECHS1 deficienciesMarie-Céline François-Heude, Elise Lebigot, Emmanuel Roze, et al.
European Journal of Pediatrics|January 26, 2002
Heterogeneity of persistent hyperinsulinaemic hypoglycaemia. A series of 175 casesPascale de Lonlay, Jean-Christophe Fournet, Guy Touati, et al.
Orphanet Journal of Rare Diseases|March 16, 2019
Betaine anhydrous in homocystinuria: results from the RoCH registryVassili Valayannopoulos, Manuel Schiff, Nathalie Guffon, et al.
Molecular Genetics and Metabolism Reports|January 21, 2021
Enteral tube feeding in patients receiving dietary treatment for metabolic diseases: A retrospective analysis in a large French cohortClaire-Marine Bérat, Célina Roda, Anais Brassier, et al.
Pageof 5