11 results on '"Giansily‐Blaizot, Muriel"'
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2. Surgery in rare bleeding disorders: the prospective MARACHI study
3. Is the coexistence of thromboembolic events and Factor VII deficiency fortuitous?
4. Transferrin Receptor-2 Gene and Non-C282Y Homozygous Patients with Hemochromatosis
5. The Clinical Severity of Alpha-2 Globin Gene Variants: Homozygosity for Hb Agrinio (HBA2: c.89T>C) Leads to Severe Antenatal Anemia, about 8 Cases in 3 Families
6. Déficit constitutionnel en facteur VII et chirurgie orthopédique majeure : entre risque hémorragique et risque thrombotique
7. Coagulation Factor Activity Level and Clinical Bleeding Severity in Rare Bleeding Disorders: Results From the European Network of Rare Bleeding Disorders (EN-RBD),
8. Replacement Therapy for Minor Surgery and Invasive Procedures in Factor VII Deficiency: The STER Experience
9. At Disease Presentation, Severity of the Bleeding Symptom Predicts the Following Bleeds in Patients with FVII Deficiency
10. The Southern French Registry of Genetic Hemochromatosis, a Tool for Determination of Clinical Prevalence and Genotype Penetrance of the Disorder.
11. Successful Treatment of Intra-Cranial Hemorrhage with Repeated Doses of Activated Recombinant FVII in a Newborn with Severe Factor VII Deficiency.
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