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You searched for: Author/Creator Fiore, Mathieu

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1. First description of an IgM monoclonal antibody causing αIIbβ3 integrin activation and acquired Glanzmann thrombasthenia associated with macrothrombocytopenia. (19th April 2019)

2. High prevalence of the natural Asn89Asp mutation in the GP1BB gene associated with Bernard–Soulier syndrome in French patients from the genetic isolate of Reunion Island. (30th January 2020)

3. A new case with Hermansky-Pudlak syndrome type 9, a rare cause of syndromic albinism with severe defect of platelets dense bodies. (3rd April 2021)

4. Evaluation of the potential utility of the total thrombus‐formation analysis system in comparison to the platelet function analyser in subjects with primary haemostatic defects. (1st July 2020)

6. Comparison of different activators of coagulation by turbidity analysis of hereditary dysfibrinogenemia and controls. Issue 2 (12th March 2021)