Mabboux I, Hary B, Courcelle S, Ceppa F, Delacour H (2016) <br />[Prolonged neuromuscular block in a patient with butyrylcholinesterase deficiency]<br /><i>Arch Pediatr</i> <b>23</b>: 497<br /><br />Delacour H, Lushchekina SV, Mabboux I, Bousquet A, Ceppa F, Schopfer LM, Lockridge O, Masson P (2014) <br />Characterization of a Novel BCHE Silent Allele: Point Mutation (p.Val204Asp) Causes Loss of Activity and Prolonged Apnea with Suxamethonium<br /><i>PLoS ONE</i> <b>9</b>: e101552<br /><br />Delacour H, Lushchekina SV, Mabboux I, Ceppa F, Masson P, Schopfer LM, Lockridge O (2014) <br />Characterization of a novel butyrylcholinesterase point mutation (p.Ala34Val), silent with mivacurium<br /><i>Biochemical Pharmacology</i> <b>92</b>: 476<br /><br />Mabboux I, Dos Santos M, Courcelle S, Hary B, Ceppa F, Delacour H (2014) <br />Rapid detection of BCHE atypical variant (p.Asp70Gly) by high resolution melting curve analysis<br /><i>Ann Biol Clin (Paris)</i> <b>72</b>: 543<br /><br />