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Results: 1-25 | 26-33 |
Results: 26-33/33

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

Authors: Mercier, B Burlot, L Ferec, C
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

Authors: Chen, JM Mercier, B Ferec, C
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
Risultati: 1-25 | 26-33 |