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Pascale de Lonlay

Showing results (31-40 of 257) with videos related to

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European Journal of Pediatrics|March 30, 2016
High glucose intake and glycaemic level in critically ill neonates with inherited metabolic disorders of intoxicationMarion Grimaud, Pascale de Lonlay, Laurent Dupic, et al.
Annals of Neurology|November 10, 2005
Pyruvate carboxylase deficiency: metabolic characteristics and new neurological aspectsAngels García-Cazorla, Daniel Rabier, Guy Touati, et al.
The Journal of Pediatrics|August 31, 2006
Mitochondrial respiratory chain deficiencies expressing the enzymatic deficiency in the hepatic tissue: a study of 31 patientsAngels Garcia-Cazorla, Pascale De Lonlay, Pierre Rustin, et al.
BMJ Open|November 23, 2019
Transcultural mediation programme in a paediatric hospital in France: qualitative and quantitative study of participants' experience and impact on hospital costsJonathan Lachal, Mélanie Escaich, Serge Bouznah, et al.
The Journal of Pediatrics|October 13, 2009
Cardiomyopathies in propionic aciduria are reversible after liver transplantationStéphane Romano, Vassili Valayannopoulos, Guy Touati, et al.
Human Mutation|September 4, 2008
Update of mutations in the genes encoding the pancreatic beta-cell K(ATP) channel subunits Kir6.2 (KCNJ11) and sulfonylurea receptor 1 (ABCC8) in diabetes mellitus and hyperinsulinismSarah E Flanagan, Séverine Clauin, Christine Bellanné-Chantelot, et al.
Journal of Inherited Metabolic Disease|March 18, 2015
Acute rhabdomyolysis and inflammationYamina Hamel, Asmaa Mamoune, François-Xavier Mauvais, et al.
La Revue Du Praticien|January 31, 2024
[New developments in neonatal screening]Michel Michel, David Cheillan, Thao Nguyen-Khoa, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|March 17, 2017
Epileptic spasms in congenital disorders of glycosylationAndreia G Pereira, Nadia Bahi-Buisson, Christine Barnerias, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|August 30, 2012
Ocular manifestations of cobalamin C type methylmalonic aciduria with homocystinuriaLeah R Fuchs, Matthieu Robert, Isabelle Ingster-Moati, et al.
Pageof 26

Showing results (31-40 of 257) with videos related to

Sort By:
Pageof 26
European Journal of Pediatrics|March 30, 2016
High glucose intake and glycaemic level in critically ill neonates with inherited metabolic disorders of intoxicationMarion Grimaud, Pascale de Lonlay, Laurent Dupic, et al.
Annals of Neurology|November 10, 2005
Pyruvate carboxylase deficiency: metabolic characteristics and new neurological aspectsAngels García-Cazorla, Daniel Rabier, Guy Touati, et al.
The Journal of Pediatrics|August 31, 2006
Mitochondrial respiratory chain deficiencies expressing the enzymatic deficiency in the hepatic tissue: a study of 31 patientsAngels Garcia-Cazorla, Pascale De Lonlay, Pierre Rustin, et al.
BMJ Open|November 23, 2019
Transcultural mediation programme in a paediatric hospital in France: qualitative and quantitative study of participants' experience and impact on hospital costsJonathan Lachal, Mélanie Escaich, Serge Bouznah, et al.
The Journal of Pediatrics|October 13, 2009
Cardiomyopathies in propionic aciduria are reversible after liver transplantationStéphane Romano, Vassili Valayannopoulos, Guy Touati, et al.
Human Mutation|September 4, 2008
Update of mutations in the genes encoding the pancreatic beta-cell K(ATP) channel subunits Kir6.2 (KCNJ11) and sulfonylurea receptor 1 (ABCC8) in diabetes mellitus and hyperinsulinismSarah E Flanagan, Séverine Clauin, Christine Bellanné-Chantelot, et al.
Journal of Inherited Metabolic Disease|March 18, 2015
Acute rhabdomyolysis and inflammationYamina Hamel, Asmaa Mamoune, François-Xavier Mauvais, et al.
La Revue Du Praticien|January 31, 2024
[New developments in neonatal screening]Michel Michel, David Cheillan, Thao Nguyen-Khoa, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|March 17, 2017
Epileptic spasms in congenital disorders of glycosylationAndreia G Pereira, Nadia Bahi-Buisson, Christine Barnerias, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|August 30, 2012
Ocular manifestations of cobalamin C type methylmalonic aciduria with homocystinuriaLeah R Fuchs, Matthieu Robert, Isabelle Ingster-Moati, et al.
Pageof 26