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