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Flora Peyvandi

Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico
University of Milan

725

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A homozygous duplication of the FGG exon 8-intron 8 junction causes congenital afibrinogenemia. Lessons learned from the study of a large consanguineous Turkish family

2021 Haematologica
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A distinct metabolic profile associated with a fatal outcome in COVID-19 patients during early epidemic in Italy

2021 medRxiv
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Human Fibrinogen Concentrate for Bleeding Prophylaxis During Surgery in Paediatric Patients with Congenital Fibrinogen Deficiency

2021
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Efficacy and Safety of Human Fibrinogen Concentrate in Patients with Congenital Fibrinogen Deficiency: Combined Results of the FORMA-02 and FORMA-04 Clinical Trials

2021
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Chromosome 3 cluster rs11385942 variant links complement activation with severe COVID-19.

2021 Journal of Autoimmunity
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Increasing levels of von Willebrand factor and factor VIII with age in patients affected by von Willebrand disease: REPLY from original authors Biguzzi et al.

2021 Journal of Thrombosis and Haemostasis
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Clinical risk scores for the early prediction of severe outocomes in patients hospitalized for COVID-19: comment.

2021 Internal and Emergency Medicine
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Impact of a commercially available DOAC absorbent on two integrated procedures for lupus anticoagulant detection.

2021 Thrombosis Research
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Pulmonary immuno-thrombosis in COVID-19 ARDS pathogenesis.

2021 Intensive Care Medicine
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Diagnosis, therapeutic advances, and key recommendations for the management of factor X deficiency

2021 Blood Reviews
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