D. Bridoux

A novel mutation in the human complex I NDUFS7 subunit associated with Leigh syndrome.

A. Munnich, A. Rötig, D. Rodriguez, 2007, Molecular genetics and metabolism.

Deoxyguanosine kinase mutations and combined deficiencies of the mitochondrial respiratory chain in patients with hepatic involvement.

A. Munnich, P. Rustin, A. Rötig, 2005, Molecular genetics and metabolism.

Glycine and ammonia plasma concentrations during sedation with remifentanil in critically ill patients

D. Benhamou, K. Asehnoune, J. Duranteau, 2007, Intensive Care Medicine.

Rapid screening of COVID‐19 patients using white blood cell scattergrams, a study on 381 patients

F. Bruneel, P. Rousselot, C. Flaujac, 2020, British journal of haematology.