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Results: 1-10 |
Results: 10
Transferrin receptor-2 gene and non-C282Y homozygous patients with hemochromatosis
Authors: Aguilar-Martinez, P Esculie-Coste, C Bismuth, M Giansily-Blaizot, M Larrey, D Schved, JF
Citation: P. Aguilar-martinez et al., Transferrin receptor-2 gene and non-C282Y homozygous patients with hemochromatosis, BL CELL M D, 27(1), 2001, pp. 290-293
Analysis of the genotypes and phenotypes of 37 unrelated patients with inherited factor VII deficiency
Authors: Giansily-Blaizot, M Aguilar-Martinez, P Biron-Andreani, C Janjean, P Igual, H Schved, JF
Citation: M. Giansily-blaizot et al., Analysis of the genotypes and phenotypes of 37 unrelated patients with inherited factor VII deficiency, EUR J HUM G, 9(2), 2001, pp. 105-112
Variable phenotypic presentation of iron overload in H63D homozygotes: aregenetic modifiers the cause?
Authors: Aguilar-Martinez, P Bismuth, M Picot, MC Thelcide, C Pageaux, GP Blanc, F Blanc, P Schved, JF Larrey, D
Citation: P. Aguilar-martinez et al., Variable phenotypic presentation of iron overload in H63D homozygotes: aregenetic modifiers the cause?, GUT, 48(6), 2001, pp. 836-842
Prevalence of HFE mutations in people from North Africa living in southernFrance
Authors: Aguilar-Martinez, P Picot, MC Becker, F Boulot, P Montoya, F Mares, P Bachelard, B Henry, Y Delarbre, JL Sarda, P Schved, JF
Citation: P. Aguilar-martinez et al., Prevalence of HFE mutations in people from North Africa living in southernFrance, BR J HAEM, 114(4), 2001, pp. 914-916
Denaturing gradient gel electrophoresis screening for mutations in the hereditary hyperferritinaemia cataract syndrome
Authors: Giansily, M Beaumont, C Desveaux, C Hetet, G Schved, JF Aguilar-Martinez, P
Citation: M. Giansily et al., Denaturing gradient gel electrophoresis screening for mutations in the hereditary hyperferritinaemia cataract syndrome, BR J HAEM, 112(1), 2001, pp. 51-54
Prenatal diagnosis of severe factor VII deficiency using mutation detection and linkage analysis
Authors: Giansily-Blaizot, M Aguilar-Martinez, P Mazurier, C Cneude, F Goudemand, J Schved, JF de Martinville, B
Citation: M. Giansily-blaizot et al., Prenatal diagnosis of severe factor VII deficiency using mutation detection and linkage analysis, BR J HAEM, 112(1), 2001, pp. 251-252
HFE mutations and transferrin receptor polymorphism analysis in porphyria cutanea tarda: a prospective study of 36 cases from southern France
Authors: Dereure, O Aguilar-Martinez, P Bessis, D Perney, P Vallat, C Guillot, B Blanc, F Guilhou, JJ
Citation: O. Dereure et al., HFE mutations and transferrin receptor polymorphism analysis in porphyria cutanea tarda: a prospective study of 36 cases from southern France, BR J DERM, 144(3), 2001, pp. 533-539
Haplotype analysis of the HFE gene: Implications for the origins of hemochromatosis related mutations (vol 25, pg 166, 1999)
Authors: Aguilar-Martinez, P Thelcide, C Jeanjean, P Masmejean, C Giansily, M Schved, JF
Citation: P. Aguilar-martinez et al., Haplotype analysis of the HFE gene: Implications for the origins of hemochromatosis related mutations (vol 25, pg 166, 1999), BL CELL M D, 26(1), 2000, pp. 112-112
Iron overload in thalassaemias and genetic haemochromatosis
Authors: Aguilar-Martinez, P Schved, JF Badens, C Thuret, I Michel, G Neonato, MG Peltier, JY Girot, R Pissard, S Galacteros, F Bachir, D Rose, C Picot, MC Denamur, E Elion, J
Citation: P. Aguilar-martinez et al., Iron overload in thalassaemias and genetic haemochromatosis, EUR J HAEMA, 64(4), 2000, pp. 279-280
Haplotype analysis of the HFE gene: Implications for the origins of hemochromatosis related mutations
Authors: Aguilar-Martinez, P Thelcide, C Jeanjean, P Masmejean, C Giansily, M Schved, JF
Citation: P. Aguilar-martinez et al., Haplotype analysis of the HFE gene: Implications for the origins of hemochromatosis related mutations, BL CELL M D, 25(11), 1999, pp. 166-169
Risultati: 1-10 |