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Unresolved hemostasis issues in haemophilia

Haemophilia : the official journal of the World Federation of Hemophilia, 2024-04, Vol.30 (S3), p.70-77

2024

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Factor VIII stimulants and other novel therapies for the treatment of von Willebrand disease: what’s new on the horizon?

Expert opinion on pharmacotherapy, 2024-07, Vol.25 (11), p.1427-1438

2024

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Immune tolerance induction in paediatric patients with haemophilia A and inhibitors receiving emicizumab prophylaxis

Haemophilia : the official journal of the World Federation of Hemophilia, 2019-09, Vol.25 (5), p.789-796

2019

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Health issues in women and girls affected by haemophilia with a focus on nomenclature, heavy menstrual bleeding, and musculoskeletal issues

Haemophilia : the official journal of the World Federation of Hemophilia, 2022-05, Vol.28 (S4), p.18-25

2022

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Pharmacokinetic parameters of recombinant factor IX Fc fusion protein are not influenced by factor IX antigen levels in subjects from the Phase 3 B‐LONG trial

Haemophilia : the official journal of the World Federation of Hemophilia, 2023-01, Vol.29 (1), p.404-407

2023

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Discussing investigational AAV gene therapy with hemophilia patients: A guide

Blood reviews, 2021-05, Vol.47, p.100759-100759, Article 100759

2021

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Hemophilia B (Factor IX Deficiency)

Hematology/oncology clinics of North America, 2021-12, Vol.35 (6), p.1143-1155

2021

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Assessment of menstrual health in adolescent and young adults with sickle cell disease

Pediatric blood & cancer, 2024-01, Vol.71 (1), p.e30727-n/a

2024

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Substitution therapy

Haemophilia : the official journal of the World Federation of Hemophilia, 2021-02, Vol.27 (S3), p.53-59

2021

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Early diagnosis of persons with von Willebrand disease using a machine learning algorithm and real-world data

Expert review of hematology, 2024-06, Vol.17 (6), p.261-268

2024

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Adequate menstrual suppression in adolescents with inherited bleeding disorders often requires multiple treatment changes: Retrospective cohort study of a multidisciplinary clinic

Pediatric blood & cancer, 2024-06, Vol.71 (6), p.e30944-n/a

2024

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Plasma factor IX: The tip of the iceberg?

Haemophilia : the official journal of the World Federation of Hemophilia, 2021-05, Vol.27 (3), p.329-331

2021

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Transitioning from emicizumab prophylaxis to valoctocogene roxaparvovec gene therapy: A simulation study for individuals with severe haemophilia A

Haemophilia : the official journal of the World Federation of Hemophilia, 2024-07, Vol.30 (4), p.905-913

2024

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Building the foundation for a community-generated national research blueprint for inherited bleeding disorders: research priorities for mucocutaneous bleeding disorders

Expert review of hematology, 2023-03, Vol.16 (sup1), p.39-54

2023

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Spontaneous bleeding and poor bleeding response with extended half‐life factor IX products: A survey of select US haemophilia treatment centres

Haemophilia : the official journal of the World Federation of Hemophilia, 2020-05, Vol.26 (3), p.e128-e129

2020

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Dental habits and oral health in children and adolescents with bleeding disorders: A single‐institution cross‐sectional study

Haemophilia : the official journal of the World Federation of Hemophilia, 2022-01, Vol.28 (1), p.73-79

2022

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Depression and anxiety in persons with Von Willebrand disease

Haemophilia : the official journal of the World Federation of Hemophilia, 2023-03, Vol.29 (2), p.545-554

2023

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A Cross-Sectional Study of Women and Girls with Congenital Bleeding Disorders: The American Thrombosis and Hemostasis Network Cohort

Journal of women's health (Larchmont, N.Y. 2002), 2020-05, Vol.29 (5), p.670-676

2020

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Bleeding patterns in patients before and after diagnosis of von Willebrand disease: Analysis of a US medical claims database

Haemophilia : the official journal of the World Federation of Hemophilia, 2022-01, Vol.28 (1), p.97-108

2022

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Characterizing female patients with haemophilia A: Administrative claims analysis and medical chart review

Haemophilia : the official journal of the World Federation of Hemophilia, 2020-05, Vol.26 (3), p.520-528

2020

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Emicizumab dose up‐titration in case of suboptimal bleeding control in people with haemophilia A

Haemophilia : the official journal of the World Federation of Hemophilia, 2023-01, Vol.29 (1), p.90-99

2023

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Von Willebrand Disease: Gaining a global perspective

Haemophilia : the official journal of the World Federation of Hemophilia, 2023-07, Vol.29 (4), p.1104-1112

2023

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Characterization of Hysterectomy/Uterine Ablation Rates in VWD and Undiagnosed Bleeding Using Claims Data [32G]

Obstetrics and gynecology (New York. 1953), 2017-05, Vol.129 (1), p.79-80S

2017

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Occurrence rates of von Willebrand disease among people receiving care in specialized treatment centres in the United States

Haemophilia : the official journal of the World Federation of Hemophilia, 2021-05, Vol.27 (3), p.445-453

2021

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Immunogenicity, safety, and efficacy of rurioctocog alfa pegol in previously untreated patients with severe hemophilia A: interim results from a phase 3, prospective, multicenter, open-label study

Expert review of hematology, 2023-10, Vol.16 (10), p.793-801

2023

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Unresolved hemostasis issues in haemophilia

Factor VIII stimulants and other novel therapies for the treatment of von Willebrand disease: what’s new on the horizon?

Immune tolerance induction in paediatric patients with haemophilia A and inhibitors receiving emicizumab prophylaxis

Health issues in women and girls affected by haemophilia with a focus on nomenclature, heavy menstrual bleeding, and musculoskeletal issues

Pharmacokinetic parameters of recombinant factor IX Fc fusion protein are not influenced by factor IX antigen levels in subjects from the Phase 3 B‐LONG trial

Discussing investigational AAV gene therapy with hemophilia patients: A guide

Hemophilia B (Factor IX Deficiency)

Assessment of menstrual health in adolescent and young adults with sickle cell disease

Substitution therapy

Early diagnosis of persons with von Willebrand disease using a machine learning algorithm and real-world data

Adequate menstrual suppression in adolescents with inherited bleeding disorders often requires multiple treatment changes: Retrospective cohort study of a multidisciplinary clinic

Plasma factor IX: The tip of the iceberg?

Transitioning from emicizumab prophylaxis to valoctocogene roxaparvovec gene therapy: A simulation study for individuals with severe haemophilia A

Building the foundation for a community-generated national research blueprint for inherited bleeding disorders: research priorities for mucocutaneous bleeding disorders

Spontaneous bleeding and poor bleeding response with extended half‐life factor IX products: A survey of select US haemophilia treatment centres

Dental habits and oral health in children and adolescents with bleeding disorders: A single‐institution cross‐sectional study

Depression and anxiety in persons with Von Willebrand disease

A Cross-Sectional Study of Women and Girls with Congenital Bleeding Disorders: The American Thrombosis and Hemostasis Network Cohort

Bleeding patterns in patients before and after diagnosis of von Willebrand disease: Analysis of a US medical claims database

Characterizing female patients with haemophilia A: Administrative claims analysis and medical chart review

Emicizumab dose up‐titration in case of suboptimal bleeding control in people with haemophilia A

Von Willebrand Disease: Gaining a global perspective

Characterization of Hysterectomy/Uterine Ablation Rates in VWD and Undiagnosed Bleeding Using Claims Data [32G]

Occurrence rates of von Willebrand disease among people receiving care in specialized treatment centres in the United States

Immunogenicity, safety, and efficacy of rurioctocog alfa pegol in previously untreated patients with severe hemophilia A: interim results from a phase 3, prospective, multicenter, open-label study

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