27 results on '"Giansily‐Blaizot, Muriel"'
Search Results
2. Surgery in rare bleeding disorders: the prospective MARACHI study
3. A newly identified ferritin L‐subunit variant results in increased proteasomal subunit degradation, impaired complex assembly, and severe hypoferritinemia.
4. Kinetics of the coagulation cascade including the contact activation system: sensitivity analysis and model reduction
5. Critical evaluation of kinetic schemes for coagulation.
6. Genotyping of five Pakistani patients with severe inherited factor X deficiency: identification of two novel mutations
7. Is the coexistence of thromboembolic events and Factor VII deficiency fortuitous?
8. The role of genetic factors in patients with hepatocellular carcinoma and iron overload – a prospective series of 234 patients
9. Life-threatening bleeding in factor VII deficiency: the role of prenatal diagnosis and primary prophylaxis
10. Homozygosity for the hyperunstable hemoglobin variant Hb Agrinio (HBA2:c.89T>C) leads to severe antenatal anemia: Eight new cases in three families.
11. A novel mutation of the β-globin gene promoter (−102 C>A) and pitfalls in family screening
12. Characterisation of a large complex intragenic re-arrangement in the FVII gene (F7) avoiding misdiagnosis in inherited factor VII deficiency
13. Prenatal diagnosis of severe factor vii deficiency using mutation detection and linkage analysis
14. Transferrin Receptor-2 Gene and Non-C282Y Homozygous Patients with Hemochromatosis
15. The EAHAD blood coagulation factor VII variant database.
16. The European Association for Haemophilia and Allied Disorders (EAHAD) Coagulation Factor Variant Databases: Important resources for haemostasis clinicians and researchers.
17. The Importance of Characterizing the Hemoglobin Instability of New Variants: The Case of Hb Dompierre [β29(B11)Gly→Arg, HBB: c.88G>C].
18. Molecular analysis of eight severe FV‐deficient patients in Pakistan: A large series of homozygous for frameshift mutations.
19. Inherited or acquired modifiers of iron status may dramatically affect the phenotype in dehydrated hereditary stomatocytosis.
20. Recombinant human factor VIIa (rFVIIa) in hemophilia: mode of action and evidence to date.
21. Variants du facteur VII de la coagulation : quelle thromboplastine utiliser pour doser son activité ?
22. Coagulation factor VII variants resistant to inhibitory antibodies.
23. Importance of Sequencing HBA1 , HBA2 and HBB Genes to Confirm the Diagnosis of High Oxygen Affinity Hemoglobin.
24. Thrombin Generation Measurement in Factor VII-Depleted Plasmas Compared to Inherited Factor VII-Deficient Plasmas.
25. Analysis of the genotypes and phenotypes of 37 unrelated patients with inherited factor VII deficiency.
26. Pharmacokinetic properties of recombinant FVIIa in inherited FVII deficiency account for a large volume of distribution at steady state and a prolonged pharmacodynamic effect.
27. Isotypic analysis of antibodies against activated Factor VII in patients with Factor VII deficiency using the x-MAP technology.
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