BERTOMORO, ANTONELLA

BERTOMORO, ANTONELLA  

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Risultati 1 - 20 di 38 (tempo di esecuzione: 0.052 secondi).
Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
A 29-year-old woman with persistent thrombocytopenia 2019 Di Pasquale, IreneBertomoro, AntonellaVianello, FabrizioBoscaro, FrancescaFabris, Fabrizio + INTERNAL AND EMERGENCY MEDICINE - -
Spontaneous recurrent intracranial haemorrhage in a woman with type 2B von Willebrand disease: A clinical case and a brief literature review 2019 Bertomoro, AntonellaMardari, RodicaSimioni, Paolo + HAEMOPHILIA - -
Spectrum of 5’UTR mutations in ANKRD26 gene in patients with inherited thrombocytopenia: c.-140C>G mutation is more frequent than expected 2017 FERRARI, SILVIALOMBARDI, ANNA-MARIABERTOMORO, ANTONELLACORTELLA, IRENEBARZON, ISABELLAGIROLAMI, ANTONIOFABRIS, FABRIZIO + PLATELETS - -
Type 2B von Willebrand disease with or without large multimers: A distinction of the two sides of the disorder is long overdue 2017 Casonato, AlessandraDaidone, VivianaGalletta, EvaBertomoro, Antonella PLOS ONE - -
Diagnostic Value of Measuring Platelet Von Willebrand Factor in Von Willebrand Disease. 2016 CASONATO, SANDRAPELOSO CATTINI, MARIA GRAZIADAIDONE, VIVIANAPONTARA, ELENABERTOMORO, ANTONELLAPRANDONI, PAOLO PLOS ONE - -
The Bleeding Assessment Tool and laboratory data in the characterisation of a female with inherited haemophilia A 2016 DAIDONE, VIVIANAGALLETTA, EVABERTOMORO, ANTONELLACASONATO, SANDRA BLOOD TRANSFUSION - -
Associated risk factors and arterial occlusions in patients with von Willebrand disease: Analysis of the literature and report of two cases 2014 GIROLAMI, ANTONIOFERRARI, SILVIABERTOMORO, ANTONELLAPERONI, EDOARDOSAMBADO, LUISACASONATO, SANDRA CASE REPORTS IN INTERNAL MEDICINE - -
An apparent silent nucleotide substitution (c.7056C>T) in the von Willebrand factor gene is responsible for type 1 von Willebrand disease. 2011 DAIDONE, VIVIANAGALLINARO, LISAPONTARA, ELENABERTOMORO, ANTONELLAPAGNAN, ANTONIOCASONATO, SANDRA + HAEMATOLOGICA - -
Reduced survival of type 2B von Willebrand factor, irrespective of large multimer representation or thrombocytopenia. 2010 CASONATO, SANDRAGALLINARO, LISAPONTARA, ELENAPADRINI, ROBERTOBERTOMORO, ANTONELLADAIDONE, VIVIANAPAGNAN, ANTONIO + HAEMATOLOGICA - -
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 - -
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 - -
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 - -
Type IIb von Willebrand disease: role of qualitative defects in atherosclerosis and endothelial dysfunction. 2007 BILORA, FRANCACASONATO, SANDRABERTOMORO, ANTONELLAGIROLAMI, ANTONIO + CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS - -
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 - -
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 - -
Fainting induces an acute increase in the concentration of plasma factor VIII and von Willebrand factor. 2003 CASONATO, SANDRAPONTARA, ELENABERTOMORO, ANTONELLAPELOSO CATTINI, MARIA GRAZIAGIROLAMI, ANTONIO + HAEMATOLOGICA - -
Lack of multimer organization of von Willebrand factor in an acquired von Willebrand syndrome. 2002 CASONATO, SANDRAPONTARA, ELENADORIA, ANDREABERTOMORO, ANTONELLAGAMBARI, PIERFRANCAGIROLAMI, ANTONIO + BRITISH JOURNAL OF HAEMATOLOGY - -
Type 2M von Willebrand disease variant characterized by abnormal von willebrand factor multimerization. 2001 CASONATO, SANDRAPONTARA, ELENASARTORELLO, FRANCESCABERTOMORO, ANTONELLAGIROLAMI, ANTONIO + JOURNAL OF LABORATORY AND CLINICAL MEDICINE - -