Mabboux I, Hary B, Courcelle S, Ceppa F, Delacour H (2016)
[Prolonged neuromuscular block in a patient with butyrylcholinesterase deficiency]
Arch Pediatr 23: 497

Delacour H, Lushchekina SV, Mabboux I, Bousquet A, Ceppa F, Schopfer LM, Lockridge O, Masson P (2014)
Characterization of a Novel BCHE Silent Allele: Point Mutation (p.Val204Asp) Causes Loss of Activity and Prolonged Apnea with Suxamethonium
PLoS ONE 9: e101552

Delacour H, Lushchekina SV, Mabboux I, Ceppa F, Masson P, Schopfer LM, Lockridge O (2014)
Characterization of a novel butyrylcholinesterase point mutation (p.Ala34Val), silent with mivacurium
Biochemical Pharmacology 92: 476

Mabboux I, Dos Santos M, Courcelle S, Hary B, Ceppa F, Delacour H (2014)
Rapid detection of BCHE atypical variant (p.Asp70Gly) by high resolution melting curve analysis
Ann Biol Clin (Paris) 72: 543