PAGLIARI, MARIA TERESA

PAGLIARI, MARIA TERESA  

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Titolo Data di pubblicazione Autori Tipo File Abstract
ADAMTS13 activity, high VWF and FVIII levels in the pathogenesis of deep vein thrombosis 1-gen-2021 Pagliari M. T.Mancini I.Bucciarelli P.Peyvandi F. + Article (author) -
The ADAMTS13-von Willebrand factor axis in COVID-19 patients 1-gen-2020 Mancini I.Baronciani L.Artoni A.Cozzi G.Novembrino C.De Zan V.Pagliari M. T.Gualtierotti R.Aliberti S.Panigada M.Grasselli G.Blasi F.Peyvandi F. + Article (author) -
Differential diagnosis between type 2A and 2B von Willebrand disease in a child with a previously undescribed de novo mutation 1-lug-2018 PAGLIARI, MARIA TERESABaronciani, L.Siboni, S. M.Payvandi, F. + Article (author) -
The dominant p.Thr274Pro mutation in the von Willebrand factor propeptide causes the von Willebrand disease type 1 phenotype in two unrelated patients 1-mar-2022 Pagliari M. T.Baronciani L.Cozzi G.Siboni S. M.Peyvandi F. + Article (author) -
Evaluation of a fully automated von Willebrand factor assay panel for the diagnosis of von Willebrand disease 1-mar-2020 Baronciani L.Bucciarelli P.Pagliari M. T.Peyvandi F. + Article (author) -
Factor V Leiden but Not Factor II 20210G>A Is a Risk Factor in a Large Cohort of Iranian Patients with Premature Coronary Artery Disease 1-lug-2020 I. ManciniM. T. PagliariE. PappalardoP. AgostiF. Peyvandi + Book Part (author) -
Next-generation sequencing and in vitro expression study of ADAMTS13 single nucleotide variants in deep vein thrombosis 1-gen-2016 Pagliari M. T.Lotta L. A.Valsecchi C.Passamonti S. M.Peyvandi F. + Article (author) -
Risk of diagnostic delay in congenital thrombotic thrombocytopenic purpura 1-apr-2019 Ferrari BPagliari MTMancini IArcudi SPayvandi F + Article (author) -
Role of ADAMTS13, VWF and F8 genes in deep vein thrombosis 1-gen-2021 Pagliari M. T.Boscarino M.Mancini I.Pappalardo E.Bucciarelli P.Peyvandi F. + Article (author) -
von Willebrand disease type 1 mutation p.Arg1379Cys and the variant p.Ala1377Val synergistically determine a 2M phenotype in four Italian patients 1-gen-2016 Pagliari M. T.Baronciani L.Cozzi G.Franchi F.Peyvandi F. + Article (author) -