S. Mesli

Succinate-CoA ligase deficiency due to mutations in SUCLA2 and SUCLG1: phenotype and genotype correlations in 71 patients

Robert W. Taylor, E. Bertini, R. Carrozzo, 2016, Journal of Inherited Metabolic Disease.

Novel Risk Factors for Premature Peripheral Arterial Occlusive Disease in Non-Diabetic Patients: A Case-Control Study

A. Bedel, J. Emmerich, M. Darmon, 2013, PloS one.

Distribution of the lipolysis stimulated receptor in adult and embryonic murine tissues and lethality of LSR-/- embryos at 12.5 to 14.5 days of gestation.

M. Landry, B. Bihain, H. Priddle, 2004, European journal of biochemistry.

Hypoketotic Hypoglycemia with Myolysis and Hypoparathyroidism: An Unusual Association in Medium Chain Acyl-CoA Desydrogenase Deficiency (MCADD)

T. Levade, M. Bloom, J. Baruteau, 2009, Journal of pediatric endocrinology & metabolism : JPEM.

Euglycemic ketoacidosis induced by therapeutic fasting in a non-diabetic patient.

V. Rigalleau, N. Foussard, K. Mohammedi, 2019, Nutrition.

Adult‐onset diagnosis of urea cycle disorders: Results of a French cohort of 71 patients

V. Rigalleau, C. Moreau, F. Mochel, 2021, Journal of inherited metabolic disease.

Sight-threatening phenylketonuric encephalopathy in a young adult, reversed by diet.

H. Gin, V. Rigalleau, C. Marchal, 2013, JIMD reports.

[Acute fatty liver in pregnancy: revealing fetal fatty acid oxidation disorders].

O. Brissaud, I. Redonnet-Vernhet, D. Carles, 2012, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Brainstem and spinal cord lesions associated with skin changes and hearing loss: think of biotinidase deficiency.

S. Rivera, S. Mesli, S. Cabasson, 2015, The Journal of pediatrics.

Energy Metabolism Rewiring Precedes UVB-Induced Primary Skin Tumor Formation.

T. Douki, W. Rachidi, R. Rossignol, 2018, Cell reports.