SARTORELLO, FRANCESCA

SARTORELLO, FRANCESCA  

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Risultati 1 - 20 di 27 (tempo di esecuzione: 0.052 secondi).
Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
Assessing Clinically Meaningful Hypercoagulability after COVID-19 Vaccination: A Longitudinal Study 2022 Campello, ElenaBulato, CristianaSimion, ChiaraSpiezia, LucaRadu, Claudia MariaGavasso, SabrinaSartorello, FrancescaSaggiorato, GraziellaTormene, DanielaSimioni, Paolo + THROMBOSIS AND HAEMOSTASIS - -
Absence of hypercoagulability after nCoV-19 vaccination: An observational pilot study 2021 Campello, ElenaSimion, ChiaraBulato, CristianaRadu, Claudia MGavasso, SabrinaSartorello, FrancescaSaggiorato, GraziellaSpiezia, LucaSimioni, Paolo + THROMBOSIS RESEARCH - -
Partial F8 gene duplication (Factor VIII Padua) associated with high factor VIII levels and familial thrombophilia 2021 Simioni, PaoloCagnin, StefanoSartorello, FrancescaSales, GabrielePagani, LucaBulato, CristianaGavasso, SabrinaChemello, FrancescoRadu, Claudia MariaTormene, DanielaSpiezia, LucaCampello, Elena + BLOOD - -
Association between ABO blood group and bleeding phenotype in patients with mild rare bleeding disorders 2018 Spiezia, LucaCampello, ElenaTURATTI, GIACOMOSIMION, CHIARAGavasso, SabrinaSaggiorato, GraziellaSartorello, FrancescaSimioni, Paolo + HAEMOPHILIA - -
Thromboelastometry hypercoagulable profiles and portal vein thrombosis in cirrhotic patients with hepatocellular carcinoma 2017 ZANETTO, ALBERTOSENZOLO, MARCOVITALE, ALESSANDROCILLO, UMBERTORADU, CLAUDIA-MARIASARTORELLO, FRANCESCASPIEZIA, LUCACAMPELLO, ELENARODRIGUEZ CASTRO, KRYSSIA ISABELFERRARESE, ALBERTOFARINATI, FABIOBURRA, PATRIZIASIMIONI, PAOLO DIGESTIVE AND LIVER DISEASE - -
Endocytosis of exogenous factor V by ex-vivo differentiated megakaryocytes from patients with severe parahaemophilia 2016 Radu, Claudia M.Spiezia, LucaBulato, CristianaGavasso, SabrinaCampello, ElenaSartorello, FrancescaSimioni, Paolo + BRITISH JOURNAL OF HAEMATOLOGY - -
Thromboelastometry profiles in patients undergoing thrombolytic therapy for acute ischaemic stroke 2016 CAMPELLO, ELENAFARINA, FILIPPO MARIASPIEZIA, LUCAMAGGIOLO, SARAPALMIERI, ANNASARTORELLO, FRANCESCABARACCHINI, CLAUDIOSIMIONI, PAOLO THROMBOSIS AND HAEMOSTASIS - -
Higher and lower active circulating VWF levels: different facets of von Willebrand disease 2015 CASONATO, SANDRAPONTARA, ELENAMORPURGO, MARGHERITASARTORELLO, FRANCESCADAIDONE, VIVIANA + BRITISH JOURNAL OF HAEMATOLOGY - -
Type 1 von Willebrand disease due to reduced von Willebrand factor synthesis and/or survival: observations from a case series. 2010 CASONATO, SANDRAGALLINARO, LISASARTORELLO, FRANCESCAPONTARA, ELENAPADRINI, ROBERTOBERTOMORO, ANTONELLADAIDONE, VIVIANAPAGNAN, ANTONIO + TRANSLATIONAL RESEARCH - -
Microsatellite (GT)(n) repeats and SNPs in the von Willebrand factor gene promoter do not influence circulating von Willebrand factor levels under normal conditions. 2009 DAIDONE, VIVIANAPONTARA, ELENASARTORELLO, FRANCESCAGALLINARO, LISASCARONI, CARLAPAGNAN, ANTONIOCASONATO, SANDRA + THROMBOSIS AND HAEMOSTASIS - -
A shorter von Willebrand factor survival in O blood group subjects explains how ABO determinants influence plasma von Willebrand factor 2008 SZTUKOWSKA, MARYTAPADRINI, ROBERTOSARTORELLO, FRANCESCAPONTARA, ELENABERTOMORO, ANTONELLADAIDONE, VIVIANAPAGNAN, ANTONIOCASONATO, SANDRA + BLOOD - -
von Willebrand factor propeptide makes it easy to identify the shorter von Willebrand factor survival in patients with type 1 and type Vicenza von Willebrand disease. 2008 GALLINARO, LISAPONTARA, ELENASARTORELLO, FRANCESCADAIDONE, VIVIANAPADRINI, ROBERTOPAGNAN, ANTONIOCASONATO, SANDRA + BRITISH JOURNAL OF HAEMATOLOGY - -
A novel von Willebrand factor mutation (11372S) associated with type 2B-like von Willebrand disease: An elusive phenotype and a difficult diagnosis 2007 CASONATO, SANDRASARTORELLO, FRANCESCAPONTARA, ELENAGALLINARO, LISABERTOMORO, ANTONELLADAIDONE, VIVIANAPAGNAN, ANTONIO + THROMBOSIS AND HAEMOSTASIS - -
Identifying carriers of type 2N von Willebrand disease: procedures and significance. 2007 CASONATO, SANDRAPONTARA, ELENASARTORELLO, FRANCESCABERTOMORO, ANTONELLAGALLINARO, LISAPAGNAN, ANTONIO + CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS - -
Multiple von Willebrand factor mutations in patients with recessive type 1 von Willebrand disease. 2007 CASONATO, SANDRAGALLINARO, LISAPONTARA, ELENASARTORELLO, FRANCESCADAIDONE, VIVIANAPAGNAN, ANTONIO + THROMBOSIS RESEARCH - -
Combined exon skipping and cryptic splice activation as a new molecular mechanism for recessive type 1 von Willebrand disease. 2006 GALLINARO, LISASARTORELLO, FRANCESCAPONTARA, ELENABERTOMORO, ANTONELLAPAGNAN, ANTONIOCASONATO, SANDRA + THROMBOSIS AND HAEMOSTASIS - -
Combined partial exon skipping and cryptic splice site activation as a new molecular mechanism for recessive type 1 von Willebrand disease. 2006 GALLINARO, LISASARTORELLO, FRANCESCAPONTARA, ELENABERTOMORO, ANTONELLAPAGNAN, ANTONIOCASONATO, SANDRA + THROMBOSIS AND HAEMOSTASIS - -
Haplotypes of Von Willebrand factor promoter predict thrombotic risk in Cushing's syndrome 2006 DAIDONE, VIVIANASARTORELLO, FRANCESCAALBIGER, NORA MARIA ELVIRAMANTERO, FRANCOPAGNAN, ANTONIOCASONATO, SANDRASCARONI, CARLA - - NA
A new L1446P mutation is responsible for impaired von Willebrand factor synthesis, structure, and function. 2004 CASONATO, SANDRAMARCATO, STEFANIASARTORELLO, FRANCESCAPONTARA, ELENAPAGNAN, ANTONIO + JOURNAL OF LABORATORY AND CLINICAL MEDICINE - -
An Arg760Cys mutation in the consensus sequence of the von Willebrand factor propeptide cleavage site is responsible for a new von Willebrand disease variant. 2003 CASONATO, SANDRASARTORELLO, FRANCESCAPONTARA, ELENABERTOMORO, ANTONELLAGIROLAMI, ANTONIO + BLOOD - -