MENEGATTI, MARZIA

MENEGATTI, MARZIA  

Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti  

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Risultati 1 - 20 di 85 (tempo di esecuzione: 0.0 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 1-gen-2021 Peyvandi, FloraMenegatti, Marzia + Article (author) -
A rare inherited coagulation disorder : combined homozygous factor VII and factor X deficiency 1-set-2004 M. MenegattiI.M. GaragiolaP.M. MannucciF. Peyvandi + Article (author) -
A recurrent Gly43Asp substitution in coagulation Factor X rigidifies its catalytic pocket and impairs catalytic activity and intracellular trafficking 1-gen-2014 M. MenegattiR. PallaF. Peyvandi + Article (author) -
A recurrent Gly43Asp substitution of coagulation Factor X rigidifies its catalytic pocket and impairs catalytic activity and intracellular trafficking 1-gen-2013 M. MenegattiR. PallaF. Peyvandi + Article (author) -
A very rare simultaneous presence of a ring chromosome 13 and a splicing site mutation on Factor X gene 1-gen-2013 M. MenegattiR. AsseltaF. Peyvandi + Article (author) -
A very rare simultaneous presence of a ring chromosome 13 and a splicing site mutation on Factor X gene 1-gen-2013 M. MenegattiR. AsseltaF. Peyvandi + Article (author) -
An international registry of patients with plasminogen deficiency (HISTORY) 1-mar-2020 Menegatti, MarziaPalla, RobertaPeyvandi, Flora + Article (author) -
Analysis of factor V in zebrafish demonstrates minimal levels needed for early hemostasis 11-giu-2019 Menegatti M.Asselta R.Duga S.Payvandi F. + Article (author) -
Arg77His and Trp187Arg are the most common mutations causing FXIII deficiency in Iran 1-gen-2012 F. PeyvandiM. Menegatti + Article (author) -
Association between thrombin generation and bleeding severity in 41 patients with coagulation factor VII deficiency 1-gen-2013 L.A. LottaS.M. SiboniM. ClericiM. MenegattiF. Peyvandi + Article (author) -
Clinical and molecular characterisation of 21 patients affected by quantitative fibrinogen deficiency 1-mar-2015 R. AsseltaG. SoldàM. MenegattiF. PeyvandiS. Duga + Article (author) -
Coagulation factor activity and clinical bleeding severity in rare bleeding disorders : results from the European Network of Rare Bleeding Disorders 1-apr-2012 F. PeyvandiR. PallaM. MenegattiS.M. Siboni + Article (author) -
Combined Factor V and Factor VIII Deficiency in Rare Coagulation Disorders 1-gen-2014 F. PeyvandiR. PallaM. Menegatti Article (author) -
Dalla diagnosi di portatrice di emofilia alla diagnosi prenatale 1-gen-2007 F. PeyvandiL. TagliabueM. MenegattiI. M. Garagiola + Working Paper -
Database on rare bleeding disorder (RBDS) : phenotype and genotype analysis on 400 affected patients 1-ago-2007 M. SpreaficoM. MenegattiI. GaragiolaR. PallaL. TagliabueR. AsseltaS. DugaP.M. MannucciF. Peyvandi + Article (author) -
Detection of Factor XIII deficiency: data from multicentre exercises amongst UK NEQAS and PRO-RBDD project laboratories 1-ago-2017 Menegatti, M.Palla, R.Peyvandi, F. + Article (author) -
Diagnosis of FXIII deficiency: data from multicentre studies amongst UK NEQAS and PRO-RBDD project laboratories 1-gen-2015 F. PeyvandiM. MenegattiR. Palla + Article (author) -
Disseminated intravascular coagulation with positive D-dimer : a controversial clinical feature in severe congenital factor XIII deficiency in southeast Iran 1-feb-2016 M. Menegatti + Article (author) -
Effect of adenosine derivatives on in vitro thrombus formation induced by shear stress 1-ago-1999 M. MenegattiP.M. MannucciPARETI, FRANCESCO INNOCENTE + Article (author) -
Effect of prothrombin 19911 A>G polymorphism on the risk of cerebral sinus-venous thrombosis 1-dic-2010 P. BucciarelliM. MenegattiP.M. Mannucci + Article (author) -