MENEGATTI, MARZIA

MENEGATTI, MARZIA  

Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti  

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Risultati 1 - 20 di 86 (tempo di esecuzione: 0.001 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
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 Peyvandi, FloraMenegatti, Marzia + Article (author) -
An international registry of patients with plasminogen deficiency (HISTORY) 2020 Menegatti, MarziaPalla, RobertaPeyvandi, Flora + Article (author) -
Rare variants lowering the levels of coagulation factor X are protective against ischemic heart disease 2020 Paraboschi, Elvezia MariaPeyvandi, FloraMenegatti, MarziaAsselta, RosannaDuga, Stefano + Article (author) -
Understanding the Impact of Aberrant Splicing in Coagulation Factor V Deficiency. 2019 Paraboschi EMMenegatti MPayvandi FDuga SAsselta R. Article (author) -
Treatment of rare factor deficiencies other than hemophilia 2019 Menegatti, MarziaPeyvandi, Flora Article (author) -
Analysis of factor V in zebrafish demonstrates minimal levels needed for early hemostasis 2019 Menegatti M.Asselta R.Duga S.Payvandi F. + Article (author) -
Molecular investigation of 41 patients affected by coagulation factor XI deficiency 2018 Rimoldi, VMenegatti, MPeyvandi, F + Article (author) -
Recombinant factor XIII A-subunit in a patient with factor XIII deficiency and recurrent pregnancy loss 2018 Menegatti, M.Payvandi, F. + Article (author) -
Potential misdiagnosis of dysfibrinogenaemia: Data from multicentre studies amongst UK NEQAS and PRO-RBDD project laboratories 2017 Menegatti, M.Palla, R.Peyvandi, F. + Article (author) -
Exploring the global landscape of genetic variation in coagulation factor XI deficiency 2017 Paraboschi, Elvezia MariaRimoldi, ValeriaMenegatti, MarziaPeyvandi, Flora + Article (author) -
Minimal factor XIII activity level to prevent major spontaneous bleeds : reply 2017 Menegatti, M.Palla, R.Bucciarelli, P.Peyvandi, F. Article (author) -
Detection of Factor XIII deficiency: data from multicentre exercises amongst UK NEQAS and PRO-RBDD project laboratories 2017 Menegatti, M.Palla, R.Peyvandi, F. + Article (author) -
Genome editing of factor X in zebrafish reveals unexpected tolerance of severe defects in the common pathway 2017 Menegatti, MarziaPeyvandi, Flora + Article (author) -
Treatment of rare factor deficiencies in 2016 2016 Peyvandi F.Menegatti M. Article (author) -
Disseminated intravascular coagulation with positive D-dimer : a controversial clinical feature in severe congenital factor XIII deficiency in southeast Iran 2016 M. Menegatti + Article (author) -
Establishment of a bleeding score as a diagnostic tool for patients with rare bleeding disorders 2016 Palla R.Siboni S. M.Menegatti M.Peyvandi F. + Article (author) -
Reduced fibrinolytic resistance in patients with factor XI deficiency : Evidence of a thrombin-independent impairment of the thrombin-activatable fibrinolysis inhibitor pathway 2016 M. MenegattiF. Peyvandi + Article (author) -
Minimal residual FXIII coagulant activity to prevent spontaneous major bleeding, on behalf of the PRO-RBDD group 2016 F. PeyvandiR. PallaM. Menegatti + Article (author) -
Inherited bleeding disorders in pregnancy : rare coagulation factor defects 2015 M. MenegattiF. PeyvandiSM. Siboni Book Part (author) -
Factor XIII deficiency : preliminary results of the PRO-RBDD project 2015 F. PeyvandiR. PallaM. MenegattiSM. Siboni + Article (author) -