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A new harmony for hemorrhagic disorders: The Dutch SYMPHONY consortium

Journal of thrombosis and haemostasis, 2022-09, Vol.20 (9), p.1984-1985

Samelson‐Jones, Benjamin J.

2022

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Haemophilia care: the only constant is change

British journal of haematology, 2021-09, Vol.194 (5), p.805-807

2021

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Andexanet alfa for reversal of rivaroxaban in a child with intracranial hemorrhage

Pediatric blood & cancer, 2022-06, Vol.69 (6), p.e29484-n/a

2022

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Digital haemophilia: Insights into the use of social media for haemophilia care, research and advocacy

Haemophilia : the official journal of the World Federation of Hemophilia, 2022-03, Vol.28 (2), p.247-253

2022

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Real‐world cost estimates of initiating emicizumab in US patients with haemophilia A

Haemophilia : the official journal of the World Federation of Hemophilia, 2021-07, Vol.27 (4), p.591-598

2021

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Factor IX assay discrepancies in the setting of liver gene therapy using a hyperfunctional variant factor IX‐Padua

Journal of thrombosis and haemostasis, 2021-05, Vol.19 (5), p.1212-1218

2021

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Adeno-Associated Virus Gene Therapy for Hemophilia

Annual review of medicine, 2023-01, Vol.74 (1), p.231-247

2023

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Comment on: Bivalirudin during thrombolysis with catheter‐directed tPA in a heparin‐refractory patient: A case report

Pediatric blood & cancer, 2020-12, Vol.67 (12), p.e28518-n/a

2020

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Novel approaches to hemophilia therapy: successes and challenges

Blood, 2017-11, Vol.130 (21), p.2251-2256

2017

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Long-Term Follow-Up of the First in Human Intravascular Delivery of AAV for Gene Transfer: AAV2-hFIX16 for Severe Hemophilia B

Molecular therapy, 2020-09, Vol.28 (9), p.2073-2082

2020

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MYH9‐macrothrombocytopenia caused by a novel variant (E1421K) initially presenting as apparent neonatal alloimmune thrombocytopenia

Pediatric blood & cancer, 2018-04, Vol.65 (4), p.n/a

2018

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Translational Potential of Immune Tolerance Induction by AAV Liver-Directed Factor VIII Gene Therapy for Hemophilia A

Frontiers in immunology, 2020-04, Vol.11, p.618-618

2020

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Activated protein C has a regulatory role in factor VIII function

Blood, 2021-05, Vol.137 (18), p.2532-2543

2021

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A Novel Murine Model Enabling rAAV8-PC Gene Therapy for Severe Protein C Deficiency

International journal of molecular sciences, 2024-10, Vol.25 (19), p.10336

2024

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Protein-Engineered Coagulation Factors for Hemophilia Gene Therapy

Molecular therapy. Methods & clinical development, 2019-03, Vol.12, p.184-201

2019

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Worldwide use of factor IX Padua for hemophilia B gene therapy

Molecular therapy, 2022-07, Vol.30 (7), p.2394-2396

Samelson-Jones, Benjamin J.

2022

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Timing of Intensive Immunosuppression Impacts Risk of Transgene Antibodies after AAV Gene Therapy in Nonhuman Primates

Molecular therapy. Methods & clinical development, 2020-06, Vol.17, p.1129-1138

2020

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Favism with methemoglobinemia

Blood, 2024-10, Vol.144 (16), p.1752-1752

2024

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Immune tolerance induction by hepatic gene transfer: First-in-human evidence

Molecular therapy, 2024-04, Vol.32 (4), p.863-864

2024

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AAV gene therapy in companion dogs with severe hemophilia: Real-world long-term data on immunogenicity, efficacy, and quality of life

Molecular therapy. Methods & clinical development, 2024-03, Vol.32 (1), p.101205-101205, Article 101205

2024

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Coagulation Factor VIII: Biological Basis of Emerging Hemophilia A Therapies

Blood, 2024-08

2024

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Multiyear Factor VIII Expression after AAV Gene Transfer for Hemophilia A

The New England journal of medicine, 2021-11, Vol.385 (21), p.1961-1973

2021

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Emerging therapies for hemophilia: controversies and unanswered questions

F1000 research, 2018, Vol.7, p.489

2018

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Analysis of vector genome integrations in multicentric lymphoma after AAV gene therapy in a severe hemophilia A dog

Molecular therapy. Methods & clinical development, 2023-12, Vol.31, p.101159-101159, Article 101159

2023

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Gene Therapy for Inherited Bleeding Disorders

Seminars in thrombosis and hemostasis, 2021-03, Vol.47 (2), p.161-173

2021

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A new harmony for hemorrhagic disorders: The Dutch SYMPHONY consortium

Haemophilia care: the only constant is change

Andexanet alfa for reversal of rivaroxaban in a child with intracranial hemorrhage

Digital haemophilia: Insights into the use of social media for haemophilia care, research and advocacy

Real‐world cost estimates of initiating emicizumab in US patients with haemophilia A

Factor IX assay discrepancies in the setting of liver gene therapy using a hyperfunctional variant factor IX‐Padua

Adeno-Associated Virus Gene Therapy for Hemophilia

Comment on: Bivalirudin during thrombolysis with catheter‐directed tPA in a heparin‐refractory patient: A case report

Novel approaches to hemophilia therapy: successes and challenges

Long-Term Follow-Up of the First in Human Intravascular Delivery of AAV for Gene Transfer: AAV2-hFIX16 for Severe Hemophilia B

MYH9‐macrothrombocytopenia caused by a novel variant (E1421K) initially presenting as apparent neonatal alloimmune thrombocytopenia

Translational Potential of Immune Tolerance Induction by AAV Liver-Directed Factor VIII Gene Therapy for Hemophilia A

Activated protein C has a regulatory role in factor VIII function

A Novel Murine Model Enabling rAAV8-PC Gene Therapy for Severe Protein C Deficiency

Protein-Engineered Coagulation Factors for Hemophilia Gene Therapy

Worldwide use of factor IX Padua for hemophilia B gene therapy

Timing of Intensive Immunosuppression Impacts Risk of Transgene Antibodies after AAV Gene Therapy in Nonhuman Primates

Favism with methemoglobinemia

Immune tolerance induction by hepatic gene transfer: First-in-human evidence

AAV gene therapy in companion dogs with severe hemophilia: Real-world long-term data on immunogenicity, efficacy, and quality of life

Coagulation Factor VIII: Biological Basis of Emerging Hemophilia A Therapies

Multiyear Factor VIII Expression after AAV Gene Transfer for Hemophilia A

Emerging therapies for hemophilia: controversies and unanswered questions

Analysis of vector genome integrations in multicentric lymphoma after AAV gene therapy in a severe hemophilia A dog

Gene Therapy for Inherited Bleeding Disorders

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