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Guidelines for the management of hemophilia

Haemophilia : the official journal of the World Federation of Hemophilia, 2013-01, Vol.19 (1), p.e1-e47

2013

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Defining extended half‐life rFVIII—A critical review of the evidence

Haemophilia : the official journal of the World Federation of Hemophilia, 2018-05, Vol.24 (3), p.348-358

2018

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Extended half-life clotting factor concentrates: results from published clinical trials

Haemophilia : the official journal of the World Federation of Hemophilia, 2016-07, Vol.22 (S5), p.25-30

2016

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Recombinant factor VIII Fc fusion protein for the prevention and treatment of bleeding in children with severe hemophilia A

Journal of thrombosis and haemostasis, 2015-06, Vol.13 (6), p.967-977

2015

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Emerging therapies for haemophilia ‐ Global perspective

Haemophilia : the official journal of the World Federation of Hemophilia, 2018-05, Vol.24 (S6), p.15-21

2018

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Safety and pharmacokinetics of anti‐TFPI antibody (concizumab) in healthy volunteers and patients with hemophilia: a randomized first human dose trial

Journal of thrombosis and haemostasis, 2015-05, Vol.13 (5), p.743-754

2015

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Deep-vein thrombosis in the era of high HIV and tuberculosis prevalence : a prospective review of its diagnosis and treatment in a quaternary centre

South African medical journal, 2017-10, Vol.107 (10), p.859-863

2017

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TRUST trial: BAY 86-6150 use in haemophilia with inhibitors and assessment for immunogenicity

Haemophilia : the official journal of the World Federation of Hemophilia, 2016-11, Vol.22 (6), p.873-879

2016

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Improved joint health in subjects with severe haemophilia A treated prophylactically with recombinant factor VIII Fc fusion protein

Haemophilia : the official journal of the World Federation of Hemophilia, 2018-01, Vol.24 (1), p.77-84

2018

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Gene and cell therapy in South Africa : current status and future prospects

South African medical journal, 2019-09, Vol.109 (8 Supplement 1), p.S13-S17

2019

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Evaluation of the utility of the ISTH-BAT in haemophilia carriers: a multinational study

Haemophilia : the official journal of the World Federation of Hemophilia, 2016-11, Vol.22 (6), p.912-918

2016

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Long-term safety and efficacy of recombinant factor VIII Fc fusion protein (rFVIIIFc) in subjects with haemophilia A

Haemophilia : the official journal of the World Federation of Hemophilia, 2016-01, Vol.22 (1), p.72-80

2016

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Recombinant factor VIIa analog in the management of hemophilia with inhibitors: results from a multicenter, randomized, controlled trial of vatreptacog alfa

Journal of thrombosis and haemostasis, 2014-08, Vol.12 (8), p.1244-1253

2014

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Changes in the amino acid sequence of the recombinant human factor VIIa analog, vatreptacog alfa, are associated with clinical immunogenicity

Journal of thrombosis and haemostasis, 2015-11, Vol.13 (11), p.1989-1998

2015

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Changes in health-related quality of life with treatment of longer-acting clotting factors: results in the A-LONG and B-LONG clinical studies

Haemophilia : the official journal of the World Federation of Hemophilia, 2016-11, Vol.22 (6), p.866-872

2016

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The predictive value of factor VIII/factor IX levels to define the severity of hemophilia: communication from the SSC of ISTH

Journal of thrombosis and haemostasis, 2018-10, Vol.16 (10), p.2106-2110

2018

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Recombinant factor VIII Fc fusion protein: extended‐interval dosing maintains low bleeding rates and correlates with von Willebrand factor levels

Journal of thrombosis and haemostasis, 2014-11, Vol.12 (11), p.1788-1800

2014

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Recombinant B‐domain‐deleted porcine sequence factor VIII (r‐pFVIII) for the treatment of bleeding in patients with congenital haemophilia A and inhibitors

Haemophilia : the official journal of the World Federation of Hemophilia, 2017-01, Vol.23 (1), p.33-41

2017

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Prophylaxis is the new standard of care in patients with haemophilia

South African medical journal, 2022-06, Vol.112 (6), p.405-408

2022

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Patient blood management : a solution for South Africa

South African medical journal, 2019-07, Vol.109 (7), p.471-476

2019

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Home therapy for inherited bleeding disorders in South Africa : results of a modified Delphi consensus process

South African medical journal, 2019-09, Vol.109 (9), p.639-644

2019

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Naturally occurring resistance mutations within the core and NS5B regions in hepatitis C genotypes, particularly genotype 5a, in South Africa

Antiviral research, 2016-03, Vol.127, p.90-98

2016

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Pharmacokinetic modelling and validation of the half‐life extension needed to reduce the burden of infusions compared with standard factor VIII

Haemophilia : the official journal of the World Federation of Hemophilia, 2018-05, Vol.24 (3), p.376-384

2018

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Low‐factor consumption for major surgery in haemophilia B with long‐acting recombinant glycoPEGylated factor IX

Haemophilia : the official journal of the World Federation of Hemophilia, 2017-01, Vol.23 (1), p.67-76

2017

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Evaluation of the self‐administered bleeding assessment tool (Self‐BAT) in haemophilia carriers and correlations with quality of life

Haemophilia : the official journal of the World Federation of Hemophilia, 2017-11, Vol.23 (6), p.e536-e538

2017

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Guidelines for the management of hemophilia

Defining extended half‐life rFVIII—A critical review of the evidence

Extended half-life clotting factor concentrates: results from published clinical trials

Recombinant factor VIII Fc fusion protein for the prevention and treatment of bleeding in children with severe hemophilia A

Emerging therapies for haemophilia ‐ Global perspective

Safety and pharmacokinetics of anti‐TFPI antibody (concizumab) in healthy volunteers and patients with hemophilia: a randomized first human dose trial

Deep-vein thrombosis in the era of high HIV and tuberculosis prevalence : a prospective review of its diagnosis and treatment in a quaternary centre

TRUST trial: BAY 86-6150 use in haemophilia with inhibitors and assessment for immunogenicity

Improved joint health in subjects with severe haemophilia A treated prophylactically with recombinant factor VIII Fc fusion protein

Gene and cell therapy in South Africa : current status and future prospects

Evaluation of the utility of the ISTH-BAT in haemophilia carriers: a multinational study

Long-term safety and efficacy of recombinant factor VIII Fc fusion protein (rFVIIIFc) in subjects with haemophilia A

Recombinant factor VIIa analog in the management of hemophilia with inhibitors: results from a multicenter, randomized, controlled trial of vatreptacog alfa

Changes in the amino acid sequence of the recombinant human factor VIIa analog, vatreptacog alfa, are associated with clinical immunogenicity

Changes in health-related quality of life with treatment of longer-acting clotting factors: results in the A-LONG and B-LONG clinical studies

The predictive value of factor VIII/factor IX levels to define the severity of hemophilia: communication from the SSC of ISTH

Recombinant factor VIII Fc fusion protein: extended‐interval dosing maintains low bleeding rates and correlates with von Willebrand factor levels

Recombinant B‐domain‐deleted porcine sequence factor VIII (r‐pFVIII) for the treatment of bleeding in patients with congenital haemophilia A and inhibitors

Prophylaxis is the new standard of care in patients with haemophilia

Patient blood management : a solution for South Africa

Home therapy for inherited bleeding disorders in South Africa : results of a modified Delphi consensus process

Naturally occurring resistance mutations within the core and NS5B regions in hepatitis C genotypes, particularly genotype 5a, in South Africa

Pharmacokinetic modelling and validation of the half‐life extension needed to reduce the burden of infusions compared with standard factor VIII

Low‐factor consumption for major surgery in haemophilia B with long‐acting recombinant glycoPEGylated factor IX

Evaluation of the self‐administered bleeding assessment tool (Self‐BAT) in haemophilia carriers and correlations with quality of life

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