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Inhibitors in Hemophilia B

Seminars in thrombosis and hemostasis, 2018-09, Vol.44 (6), p.578-589

2018

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Prophylaxis in people with haemophilia

Thrombosis and haemostasis, 2009-04, Vol.101 (4), p.674-681

2009

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The association between unemployment and treatment among adults with hemophilia

Research and practice in thrombosis and haemostasis, 2024-07, Vol.8 (5), p.102514, Article 102514

2024

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The management of hemophilia in elderly patients

Clinical interventions in aging, 2007-01, Vol.2 (3), p.361-368

2007

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Clinical use of Haemate(R) P in inherited von Willebrand's disease: a cohort study on 100 Italian patients

Haematologica (Roma), 2007-07, Vol.92 (7), p.944-951

2007

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Identification of the Profile of the Patients with Hemophilia B Eligible for Treatment with Nonacog Alfa Once-Weekly

Reports (MDPI), 2020-03, Vol.3 (1), p.3

2020

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Very high risk of intracranial hemorrhage and severe outcomes in adult patients with mild hemophilia: Sub-analysis of the EMO.REC Registry

Thrombosis research, 2023-01, Vol.221, p.35-36

2023

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Long-acting recombinant coagulation factor IX albumin fusion protein (rIX-FP) in hemophilia B: results of a phase 3 trial

Blood, 2016-04, Vol.127 (14), p.1761-1769

2016

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Experience of secondary prophylaxis in 20 adolescent and adult Italian hemophiliacs

Thrombosis and haemostasis, 2006-10, Vol.96 (4), p.542-543

2006

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Confronting COVID-19: Issues in Hemophilia and Congenital Bleeding Disorders

Seminars in thrombosis and hemostasis, 2020-10, Vol.46 (7), p.819-822

2020

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Cumulative inhibitor incidence in previously untreated patients with severe hemophilia A treated with plasma-derived versus recombinant factor VIII concentrates: A critical systematic review

Critical reviews in oncology/hematology, 2012-01, Vol.81 (1), p.82-93

2012

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FEIBA versus NovoSeven in hemophilia patients with inhibitors

Seminars in thrombosis and hemostasis, 2013-10, Vol.39 (7), p.772-778

2013

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Therapeutic choices in persons with haemophilia at the time of COVID-19

Blood transfusion = Trasfusione del sangue, 2020-07, Vol.18 (4), p.326-327

2020

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Development and definition of a simplified scanning procedure and scoring method for Haemophilia Early Arthropathy Detection with Ultrasound (HEAD-US)

Thrombosis and haemostasis, 2013-06, Vol.109 (6), p.1170-1179

2013

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Analysis of the structural effects of four novel and a previously known mutations causing factor XI deficiency

Thrombosis and haemostasis, 2009-09, Vol.102 (3), p.603-606

2009

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Systematic review of the role of FVIII concentrates in inhibitor development in previously untreated patients with severe hemophilia a: a 2013 update

Seminars in thrombosis and hemostasis, 2013-10, Vol.39 (7), p.752-766

2013

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Prophylaxis in children with hemophilia: evidence-based achievements, old and new challenges

Seminars in thrombosis and hemostasis, 2012-02, Vol.38 (1), p.79-94

2012

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Controversies in Inherited Bleeding Disorders

Seminars in thrombosis and hemostasis, 2016-07, Vol.42 (5), p.459-462

2016

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Alloantibodies and Congenital Bleeding Disorders: New Insights in the Pathogenesis and Management

Seminars in thrombosis and hemostasis, 2018-09, Vol.44 (6), p.505-508

2018

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Severe bleeding in a patient with factor XIII deficiency and COVID‐19

Haemophilia : the official journal of the World Federation of Hemophilia, 2021-01, Vol.27 (1), p.e140-e142

2021

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F7 gene variants modulate protein levels in a large cohort of patients with factor VII deficiency. Results from a genotype-phenotype study

Thrombosis and haemostasis, 2017-08, Vol.117 (8), p.1455-1464

2017

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Optimising prophylaxis outcomes and costs in haemophilia patients switching to recombinant FVIII-Fc: a single-centre real-world experience

Blood transfusion = Trasfusione del sangue, 2020-09, Vol.18 (5), p.374-385

2020

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Benefits of prophylaxis versus on-demand treatment in adolescents and adults with severe haemophilia A: the POTTER study

Thrombosis and haemostasis, 2015-07, Vol.114 (1), p.35-45

2015

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The effect of carriers’ reproductive choices and pregnancy history on sporadic severe haemophilia: A 20‐year retrospective study through a regional registry

Haemophilia : the official journal of the World Federation of Hemophilia, 2022-03, Vol.28 (2), p.308-315

2022

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Improving assessment and management of pain in hemophilia: an Italian Delphi consensus statement

Blood reviews, 2022-01, Vol.51, p.100885-100885, Article 100885

2022

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Inhibitors in Hemophilia B

Prophylaxis in people with haemophilia

The association between unemployment and treatment among adults with hemophilia

The management of hemophilia in elderly patients

Clinical use of Haemate(R) P in inherited von Willebrand's disease: a cohort study on 100 Italian patients

Identification of the Profile of the Patients with Hemophilia B Eligible for Treatment with Nonacog Alfa Once-Weekly

Very high risk of intracranial hemorrhage and severe outcomes in adult patients with mild hemophilia: Sub-analysis of the EMO.REC Registry

Long-acting recombinant coagulation factor IX albumin fusion protein (rIX-FP) in hemophilia B: results of a phase 3 trial

Experience of secondary prophylaxis in 20 adolescent and adult Italian hemophiliacs

Confronting COVID-19: Issues in Hemophilia and Congenital Bleeding Disorders

Cumulative inhibitor incidence in previously untreated patients with severe hemophilia A treated with plasma-derived versus recombinant factor VIII concentrates: A critical systematic review

FEIBA versus NovoSeven in hemophilia patients with inhibitors

Therapeutic choices in persons with haemophilia at the time of COVID-19

Development and definition of a simplified scanning procedure and scoring method for Haemophilia Early Arthropathy Detection with Ultrasound (HEAD-US)

Analysis of the structural effects of four novel and a previously known mutations causing factor XI deficiency

Systematic review of the role of FVIII concentrates in inhibitor development in previously untreated patients with severe hemophilia a: a 2013 update

Prophylaxis in children with hemophilia: evidence-based achievements, old and new challenges

Controversies in Inherited Bleeding Disorders

Alloantibodies and Congenital Bleeding Disorders: New Insights in the Pathogenesis and Management

Severe bleeding in a patient with factor XIII deficiency and COVID‐19

F7 gene variants modulate protein levels in a large cohort of patients with factor VII deficiency. Results from a genotype-phenotype study

Optimising prophylaxis outcomes and costs in haemophilia patients switching to recombinant FVIII-Fc: a single-centre real-world experience

Benefits of prophylaxis versus on-demand treatment in adolescents and adults with severe haemophilia A: the POTTER study

The effect of carriers’ reproductive choices and pregnancy history on sporadic severe haemophilia: A 20‐year retrospective study through a regional registry

Improving assessment and management of pain in hemophilia: an Italian Delphi consensus statement

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