PAYVANDI, FLORA

PAYVANDI, FLORA  

Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti  

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Titolo Data di pubblicazione Autori Tipo File Abstract
A case of ceftazidime-related myoclonus 1-ott-2020 E. PagliaroP. AgostiF. Peyvandi + Book Part (author) -
A comparative evaluation of a new automated assay for von Willebrand factor activity 1-gen-2013 F. Peyvandi + Article (author) -
A comparative evaluation of a new fully automated assay for von Willebrand factor collagen binding activity to an established method 1-gen-2018 Baronciani, L.Peyvandi, F. + Article (author) -
A critical appraisal of one-stage and chromogenic assays of factor VIII activity 1-feb-2016 F. Peyvandi + Article (author) -
A critical role for Gly25 in the B chain of human thrombin 1-gen-2005 F. PeyvandiP.M. Mannucci + Article (author) -
A fatal case of COVID-19 pneumonia occurring in a patient with severe acute ulcerative colitis 1-gen-2020 Mazza S.Sorce A.Peyvandi F.Vecchi M.Caprioli F. Article (author) -
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 homozygous is bp insertion in the human factor vu gene results in modification of a calcium binding site and reduced secretion/function 1-gen-2000 Peyvandi F. Article (author) -
A natural prothrombin mutant reveals an unexpected influence of the A-chain's structure on the activity of human α-thrombin 1-gen-2004 F. PeyvandiP.M. Mannucci + Article (author) -
A new hemophilia carrier nomenclature to define hemophilia in women and girls: Communication from the SSC of the ISTH 1-ago-2021 Peyvandi F. + Article (author) -
A novel CD46 mutation in a patient with microangiopathy clinically resembling thrombotic thrombocytopenic purpura and normal ADAMTS13 activity 1-gen-2015 R. RossioL.A. LottaI. GaragiolaM. CugnoF. Peyvandi + Article (author) -
A novel mutation of alpha2-plasmin inhibitor gene causes an inherited deficiency and a bleeding tendency 1-gen-2008 A. MainoI. GaragiolaA. ArtoniF. Peyvandi + Article (author) -
A novel polymorphism in intron 1a of the human factor VII gene (G73A): study of a healthy Italian population and of 190 young survivors of myocardial infarction 1-feb-2000 F. PeyvandiP.M. MannucciP. Bucciarelli + Article (author) -
A Randomized Trial of Factor VIII and Neutralizing Antibodies in Hemophilia A 26-mag-2016 F. PeyvandiP.M. MannucciI. GaragiolaM.E. Mancuso + 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 F8 mutation (c.6046C>T) causing hemophilia A in 8% of northern Italian patients : evidence for a founder effect 1-mar-2016 I. GaragiolaMORTARINO, MIMOSAM.E. MancusoFASULO, MARIA ROSARIAF. 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 synonymous (c.3390C>T) or a splice-site (c.3380-2A>G) mutation causes exon 26 skipping in four patients with von Willebrand disease (2A/IIE) 1-gen-2013 L. BaroncianiM. SolimandoS. La MarcaG. CozziF. Peyvandi + Article (author) -
A two-centre comparative evaluation of new automated assays for von Willebrand factor ristocetin cofactor activity and antigen 1-gen-2013 S. La MarcaBERBENNI, PAOLA ERNESTA CARMELAL. BaroncianiF. Peyvandi + Article (author) -