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Albumin-Fusion Recombinant FIX in the Management of People with Hemophilia B: An Evidence-Based Review

Drug design, development and therapy, 2022-01, Vol.16, p.3109-3116

2022

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CO62 Prophylaxis Treatment for Patients With Hemophilia A Without Inhibitors: Experience Monitoring Survey on the Use of Damoctocog Alfa Pegol

Value in health, 2022-12, Vol.25 (12), p.S29-S29

Zanon, E

2022

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Type 3 von Willebrand disease mistaken for moderate haemophilia A: a lesson still to be learned

Haemophilia : the official journal of the World Federation of Hemophilia, 2018-05, Vol.24 (3), p.e154-e157

2018

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Pharmacokinetics of plasma-derived vs. recombinant FVIII concentrates: a comparative study

Haemophilia : the official journal of the World Federation of Hemophilia, 2015-03, Vol.21 (2), p.204-209

2015

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Cerebrovascular diseases in hemophiliacs: A real, but underestimated risk

Haemophilia : the official journal of the World Federation of Hemophilia, 2018-01, Vol.24 (1), p.e3-e5

2018

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Potential biomarkers of haemophilic arthropathy: correlations with compatible additive magnetic resonance imaging scores

Haemophilia : the official journal of the World Federation of Hemophilia, 2016-09, Vol.22 (5), p.760-764

2016

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Controlled, cross-sectional MRI evaluation of joint status in severe haemophilia A patients treated with prophylaxis vs. on demand

Haemophilia : the official journal of the World Federation of Hemophilia, 2015-03, Vol.21 (2), p.171-179

2015

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Comorbidities in persons with haemophilia aged 60 years or more compared with age‐matched people from the general population

Haemophilia : the official journal of the World Federation of Hemophilia, 2018-01, Vol.24 (1), p.e6-e10

2018

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Combined use of antifibrinolytics and activated prothrombin complex concentrate (aPCC) is not related to thromboembolic events in patients with acquired haemophilia A: data from FAIR Registry

Journal of thrombosis and thrombolysis, 2019-01, Vol.47 (1), p.129-133

2019

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Effects of secondary prophylaxis started in adolescent and adult haemophiliacs

Haemophilia : the official journal of the World Federation of Hemophilia, 2008-09, Vol.14 (5), p.945-951

2008

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Confronting the psychological burden of haemophilia

Haemophilia : the official journal of the World Federation of Hemophilia, 2011-01, Vol.17 (1), p.21-27

2011

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Natural history and clinical characteristics of inhibitors in previously treated haemophilia A patients: a case series

Haemophilia : the official journal of the World Federation of Hemophilia, 2017-03, Vol.23 (2), p.255-263

2017

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Intracranial haemorrhage in the Italian population of haemophilia patients with and without inhibitors

Haemophilia : the official journal of the World Federation of Hemophilia, 2012-01, Vol.18 (1), p.39-45

2012

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Effects of recurrent disturbances on the periphyton community downstream of a dammed watercourse

Brazilian journal of biology, 2013-05, Vol.73 (2), p.253-258

2013

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Ultrasonographically-guided fine-needle aspiration of axillary lymph nodes: role in breast cancer management

British journal of cancer, 2003-03, Vol.88 (5), p.702-706

2003

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A completely automated CAD system for mass detection in a large mammographic database

Medical physics (Lancaster), 2006-08, Vol.33 (8), p.3066-3075

2006

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Efficacy and safety of highly purified, doubly virus-inactivated VWF/FVIII concentrates in inherited von Willebrand's disease: results of an Italian cohort study on 120 patients characterized by bleeding severity score

Haemophilia : the official journal of the World Federation of Hemophilia, 2010-01, Vol.16 (1), p.101-110

2010

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Whole blood rotation thromboelastometry (ROTEM®) in nine severe factor V deficient patients and evaluation of the role of intraplatelets factor V

Haemophilia : the official journal of the World Federation of Hemophilia, 2012-05, Vol.18 (3), p.463-468

2012

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Efficacy and safety during formulation switch of a pasteurized VWF/FVIII concentrate: results from an Italian prospective observational study in patients with von Willebrand disease

Haemophilia : the official journal of the World Federation of Hemophilia, 2013-01, Vol.19 (1), p.82-88

2013

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Central nervous system bleeding in patients with rare bleeding disorders

Haemophilia : the official journal of the World Federation of Hemophilia, 2012-01, Vol.18 (1), p.34-38

2012

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Endothelial dysfunction in haemophilia patients

Haemophilia : the official journal of the World Federation of Hemophilia, 2008-09, Vol.14 (5), p.1055-1062

2008

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Perceived challenges and attitudes to regimen and product selection from Italian haemophilia treaters: the 2013 AICE survey

Haemophilia : the official journal of the World Federation of Hemophilia, 2014-03, Vol.20 (2), p.e128-e135

2014

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Information to cancer patients: a questionnaire survey in three different geographical areas in Italy

Supportive care in cancer, 2008-08, Vol.16 (8), p.869-877

2008

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Garças Reservoir trophic state dynamics: a 20-year synthesis

Hoehnea, 2020, Vol.47

2020

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Pregnancy and oral contraceptives in factor V deficiency: a study of 22 patients (five homozygotes and 17 heterozygotes) and review of the literature

Haemophilia : the official journal of the World Federation of Hemophilia, 2005-01, Vol.11 (1), p.26-30

2005

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Albumin-Fusion Recombinant FIX in the Management of People with Hemophilia B: An Evidence-Based Review

CO62 Prophylaxis Treatment for Patients With Hemophilia A Without Inhibitors: Experience Monitoring Survey on the Use of Damoctocog Alfa Pegol

Type 3 von Willebrand disease mistaken for moderate haemophilia A: a lesson still to be learned

Pharmacokinetics of plasma-derived vs. recombinant FVIII concentrates: a comparative study

Cerebrovascular diseases in hemophiliacs: A real, but underestimated risk

Potential biomarkers of haemophilic arthropathy: correlations with compatible additive magnetic resonance imaging scores

Controlled, cross-sectional MRI evaluation of joint status in severe haemophilia A patients treated with prophylaxis vs. on demand

Comorbidities in persons with haemophilia aged 60 years or more compared with age‐matched people from the general population

Combined use of antifibrinolytics and activated prothrombin complex concentrate (aPCC) is not related to thromboembolic events in patients with acquired haemophilia A: data from FAIR Registry

Effects of secondary prophylaxis started in adolescent and adult haemophiliacs

Confronting the psychological burden of haemophilia

Natural history and clinical characteristics of inhibitors in previously treated haemophilia A patients: a case series

Intracranial haemorrhage in the Italian population of haemophilia patients with and without inhibitors

Effects of recurrent disturbances on the periphyton community downstream of a dammed watercourse

Ultrasonographically-guided fine-needle aspiration of axillary lymph nodes: role in breast cancer management

A completely automated CAD system for mass detection in a large mammographic database

Efficacy and safety of highly purified, doubly virus-inactivated VWF/FVIII concentrates in inherited von Willebrand's disease: results of an Italian cohort study on 120 patients characterized by bleeding severity score

Whole blood rotation thromboelastometry (ROTEM®) in nine severe factor V deficient patients and evaluation of the role of intraplatelets factor V

Efficacy and safety during formulation switch of a pasteurized VWF/FVIII concentrate: results from an Italian prospective observational study in patients with von Willebrand disease

Central nervous system bleeding in patients with rare bleeding disorders

Endothelial dysfunction in haemophilia patients

Perceived challenges and attitudes to regimen and product selection from Italian haemophilia treaters: the 2013 AICE survey

Information to cancer patients: a questionnaire survey in three different geographical areas in Italy

Garças Reservoir trophic state dynamics: a 20-year synthesis

Pregnancy and oral contraceptives in factor V deficiency: a study of 22 patients (five homozygotes and 17 heterozygotes) and review of the literature

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