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Marzia Menegatti

Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico
University of Milan

71

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1662

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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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An international registry of patients with plasminogen deficiency (HISTORY)

2020 Haematologica
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Clinical and laboratory diagnosis of rare coagulation disorders (RCDs)

2019 Thrombosis Research
- Marzia Menegatti
- Roberta Palla
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Rare variants lowering the levels of coagulation factor X are protective against ischemic heart disease

2019 Haematologica
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Understanding the Impact of Aberrant Splicing in Coagulation Factor V Deficiency

2019 International Journal of Molecular Sciences
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Analysis of factor V in zebrafish demonstrates minimal levels needed for early hemostasis

2019 Blood Advances
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Analysis of factor V in zebrafish demonstrates minimal levels needed for hemostasis and risk stratifies human variants

2019 bioRxiv
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Management of rare acquired bleeding disorders

2019 Hematology
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Profiling the mutational landscape of coagulation factor V deficiency

2019 Haematologica
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Treatment of rare factor deficiencies other than hemophilia

2019 Blood
- Marzia Menegatti
- Flora Peyvandi
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Citations (36)