Muriel Giansily-Blaizot

7PUBLICATIONS
29CO-AUTHORS
Cardiovascular medicine and haematology not elsewhere classifiedCardiology (incl. cardiovascular diseases)Nuclear engineering (incl. fuel enrichment and waste processing and storage)HaematologyEpigenetics (incl. genome methylation and epigenomics)
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Publications (7)

|Jul 21, 2026
Genetic and Laboratory Predictors of Bleeding Severity in FVII Deficiency: Insights from PRO-RBDD and EN-RBD Databases.

|Jan 29, 2024
Congenital fibrinogen disorders: a retrospective clinical and genetic analysis of the Prospective Rare Bleeding Disorders Database.

Samin Mohsenian, Roberta Palla, Marzia Menegatti

|Oct 23, 2023
A newly identified ferritin L-subunit variant results in increased proteasomal subunit degradation, impaired complex assembly, and severe hypoferritinemia.

Dayana Shagidov, Noga Guttmann-Raviv, Séverine Cunat

|Jan 21, 2022
Importance of Sequencing HBA1, HBA2 and HBB Genes to Confirm the Diagnosis of High Oxygen Affinity Hemoglobin.

Mathilde Filser, Betty Gardie, Mathieu Wemeau

|Apr 26, 2020
The EAHAD blood coagulation factor VII variant database.

Muriel Giansily-Blaizot, Pavithra M Rallapalli, Stephen J Perkins

|Mar 14, 2020
The European Association for Haemophilia and Allied Disorders (EAHAD) Coagulation Factor Variant Databases: Important resources for haemostasis clinicians and researchers.

John H McVey, Pavithra M Rallapalli, Geoffrey Kemball-Cook

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Frequent Collaborators

2 joint publications

Munira Borhany

2 joint publications

John H McVey

2 joint publications

Pavithra M Rallapalli

2 joint publications

Geoffrey Kemball-Cook