Authors:
Billon, S
Escoffre-Barbe, M
Mercier, B
Abgrall, JF
Ferec, C
Citation: S. Billon et al., Fibrinogen is not an additional risk factor of thromboembolic disease in factor V Leiden patients, THROMB HAEM, 81(4), 1999, pp. 659-660
Authors:
Lefrere, JJ
Cantaloube, JF
Defer, C
Mercier, B
Loiseau, P
Vignon, D
Pawlotsky, JM
Biagini, P
Lerable, J
Rouger, P
Roudot-Thoraval, F
Ferec, C
Citation: Jj. Lefrere et al., Screening for HBV, HCV and HIV genomes in blood donations: shortcomings ofpooling revealed by a multicentre study simulating real-time testing, J VIROL MET, 80(1), 1999, pp. 33-44
Citation: B. Mercier et al., Simultaneous screening for HBV DNA and HCV RNA genomes in blood donations using a novel TaqMan PCR assay, J VIROL MET, 77(1), 1999, pp. 1-9
Authors:
Lefrere, JJ
Ferec, C
Roudot-Thoraval, F
Loiseau, P
Cantaloube, JF
Biagini, P
Mariotti, M
LeGac, G
Mercier, B
Citation: Jj. Lefrere et al., GBV-C/hepatitis G virus (HGV) RNA load in immunodeficient individuals and in immunocompetent individuals, J MED VIROL, 59(1), 1999, pp. 32-37
Authors:
Mercier, B
Barclais, A
Botte, C
Cantalube, JF
Coste, J
Defer, C
Gautreau, C
Giannoli, C
Halfon, P
Lepot, I
Loiseau, P
Martial, J
Montcharmont, P
Merel, P
Ouzan, D
Ravera, N
Follana, J
Cesaire, R
Janot, C
Lemaire, JM
De Micco, P
Vezon, G
Ferec, C
Citation: B. Mercier et al., Prevalence of GBV C HGV RNA and GBV C HGV antibodies in French volunteer blood donors: Results of a collaborative study, VOX SANGUIN, 76(3), 1999, pp. 166-169
Authors:
Chen, JM
Audrezet, ME
Mercier, B
Quere, I
Ferec, C
Citation: Jm. Chen et al., Exclusion of anionic trypsinogen and mesotrypsinogen involvement in hereditary pancreatitis without cationic trypsinogen gene mutations, SC J GASTR, 34(8), 1999, pp. 831-832
Authors:
Ferec, C
Raguenes, O
Salomon, R
Roche, C
Bernard, JP
Guillot, M
Quere, I
Faure, C
Mercier, B
Audrezet, MP
Guillausseau, PJ
Dupont, C
Munnich, A
Bignon, JD
Le Bodic, L
Citation: C. Ferec et al., Mutations in the cationic trypsinogen gene and evidence for genetic heterogeneity in hereditary pancreatitis, J MED GENET, 36(3), 1999, pp. 228-232
Citation: Jm. Chen et al., Strong evidence that the N21I substitution in the cationic trypsinogen gene causes disease in hereditary pancreatitis, GUT, 45(6), 1999, pp. 916-916