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Results:
1-16
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Results: 16
Authors:
Le Marechal, C
Audrezet, MP
Quere, I
Raguenes, O
Langonne, S
Ferec, C
Citation: C. Le Marechal et al., Complete and rapid scanning of the cystic fibrosis transmembrane conductance regulator (CFTR) gene by denaturing high-performance liquid chromatography (D-HPLC): major implications for genetic counselling, HUM GENET, 108(4), 2001, pp. 290-298
Authors:
Gris, JC
Jamin, C
Benifla, JL
Quere, I
Madelenat, P
Mares, P
Citation: Jc. Gris et al., APC resistance and third-generation oral contraceptives - Acquired resistance to activated protein C, oral contraceptives and the risk of thromboembolic disease, HUM REPR, 16(1), 2001, pp. 3-8
Authors:
Chen, JM
Mercier, B
Audrezet, MP
Raguenes, O
Quere, I
Ferec, C
Citation: Jm. Chen et al., Mutations of the pancreatic secretory trypsin inhibitor (PSTI) gene in idiopathic chronic pancreatitis, GASTROENTY, 120(4), 2001, pp. 1061-1063
Authors:
Quere, I
Mercier, E
Bellet, H
Janbon, C
Mares, P
Gris, JC
Citation: I. Quere et al., Vitamin supplementation and pregnancy outcome in women with recurrent early pregnancy loss and hyperhomocysteinemia, FERT STERIL, 75(4), 2001, pp. 823-825
Authors:
Chen, JM
Bis, AP
Le Bodic, L
Ruszniewski, P
Robaszkiewicz, M
Deprez, PH
Raguenes, O
Quere, I
Andriulli, A
Ferec, C
Citation: Jm. Chen et al., Mutational screening of the cationic trypsinogen gene in a large cohort ofsubjects with idiopathic chronic pancreatitis, CLIN GENET, 59(3), 2001, pp. 189-193
Authors:
Scotet, V
De Braekeleer, M
Audrezet, MP
Lode, L
Verlingue, C
Quere, I
Mercier, B
Dugueperoux, I
Codet, JP
Moineau, MP
Parent, P
Ferec, C
Citation: V. Scotet et al., Prevalence of CFTR mutations in hypertrypsinaemia detected through neonatal screening for cystic fibrosis, CLIN GENET, 59(1), 2001, pp. 42-47
Authors:
Perrichot, R
Mercier, B
Quere, I
Carre, A
Simon, P
Whebe, B
Cledes, J
Ferec, C
Citation: R. Perrichot et al., Novel mutations in the duplicated region of PKD1 gene, EUR J HUM G, 8(5), 2000, pp. 353-359
Authors:
Gris, JC
Quere, I
Sanmarco, M
Boutiere, B
Mercier, E
Amiral, J
Hubert, AM
Ripart-Neveu, S
Hoffet, M
Tailland, ML
Rousseau, O
Monpeyroux, F
Dauzat, M
Sampol, J
Daures, JP
Berlan, J
Mares, P
Citation: Jc. Gris et al., Antiphospholipid and antiprotein syndromes in non-thrombotic, non-autoimmune women with unexplained recurrent primary early foetal loss - The Nimes Obstetricians and Haematologists Study(4) NOHA(4), THROMB HAEM, 84(2), 2000, pp. 228-236
Authors:
Quere, I
Citation: I. Quere, Should we consider hyperhomocystinemia as a factor of vascular risk?, REV MED IN, 21(3), 2000, pp. 229-230
Authors:
Scotet, V
de Braekeleer, M
Roussey, M
Rault, G
Parent, P
Dagorne, M
Journel, H
Lemoigne, A
Codet, JP
Catheline, M
David, V
Chaventre, A
Dugueperoux, I
Verlingue, C
Quere, I
Mercier, B
Audrezet, MP
Ferec, C
Citation: V. Scotet et al., Neonatal screening for cystic fibrosis in Brittany, France: assessment of 10 years' experience and impact on prenatal diagnosis, LANCET, 356(9232), 2000, pp. 789-794
Authors:
Degraeve, F
Quere, I
Dereure, O
Gris, JC
Dignat-Georges, F
Durand, L
Janbon, C
Citation: F. Degraeve et al., Cutaneous thrombotic and necrotizing microangiopathy revealing a large granular lymphocytic leukaemia, BR J DERM, 143(2), 2000, pp. 445-446
Authors:
Gris, JC
Quere, I
Monpeyroux, F
Mercier, E
Ripart-Neveu, S
Tailland, ML
Hoffet, M
Berlan, J
Daures, JP
Mares, P
Citation: Jc. Gris et al., Case-control study of the frequency of thrombophilic disorders in couples with late foetal loss and no thrombotic antecedent - The nimes obstetricians and haematologists study (NOHA), THROMB HAEM, 81(6), 1999, pp. 891-899
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:
Mercier, E
Quere, I
Chabert, R
Lallemant, JG
Daures, JP
Berlan, J
Gris, JC
Citation: E. Mercier et al., The 20210A allele of the prothrombin gene is an independent risk factor for perception deafness in patients with venous thromboembolic antecedents, BLOOD, 93(9), 1999, pp. 3150-3152
Authors:
Quere, I
Paul, V
Rouillac, C
Janbon, C
London, J
Demaille, J
Kamoun, P
Dufier, JL
Abitbol, M
Chasse, JF
Citation: I. Quere et al., Spatial and temporal expression of the cystathionine beta-synthase gene during early human development, BIOC BIOP R, 254(1), 1999, pp. 127-137
Risultati:
1-16
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