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Mitochondrion|March 4, 2010
New SUCLG1 patients expanding the phenotypic spectrum of this rare cause of mild methylmalonic aciduriaVassili Valayannopoulos, Coralie Haudry, Valérie Serre, et al.Biochemia Medica|April 30, 2021
Recommendations for the application and follow-up of quality controls in medical laboratoriesJean-Marc Giannoli, Stéphanie Albarede, Thierry Avellan, et al.Annales De Biologie Clinique|October 23, 2019
[Recommendations for the application and the follow-up of quality controls in medical biology laboratories]Jean-Marc Giannoli, Stéphanie Albarede, Thierry Avellan, et al.Journal of Inherited Metabolic Disease|October 28, 2010
Multiple sources of metabolic disturbance in ETHE1-related ethylmalonic encephalopathyMagalie Barth, Chris Ottolenghi, Laurence Hubert, et al.Clinical Chemistry and Laboratory Medicine|October 18, 2016
Recommendation for the review of biological reference intervals in medical laboratoriesJoseph Henny, Anne Vassault, Guilaine Boursier, et al.Clinical Journal of the American Society of Nephrology : CJASN|September 1, 2012
L-carnitine treatment in incident hemodialysis patients: the multicenter, randomized, double-blinded, placebo-controlled CARNIDIAL trialLucile Mercadal, Mathieu Coudert, Anne Vassault, 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.Pageof 2