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Comment on: Interpreting data on inhibitor development from previously untreated patient studies, beware of premature conclusions

Haemophilia : the official journal of the World Federation of Hemophilia, 2018-07, Vol.24 (4), p.e273-e275

Liesner, Dr R.J

2018

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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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Prophylactic treatment of bleeding episodes in children <12 years with moderate to severe hereditary factor X deficiency (FXD): Efficacy and safety of a high‐purity plasma‐derived factor X (pdFX) concentrate

Haemophilia : the official journal of the World Federation of Hemophilia, 2018-11, Vol.24 (6), p.941-949

2018

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Treatment of bleeding episodes in haemophilia A complicated by a factor VIII inhibitor in patients receiving Emicizumab. Interim guidance from UKHCDO Inhibitor Working Party and Executive Committee

Haemophilia : the official journal of the World Federation of Hemophilia, 2018-05, Vol.24 (3), p.344-347

2018

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A phenotype–genotype correlation of ADAMTS13 mutations in congenital thrombotic thrombocytopenic purpura patients treated in the United Kingdom

Journal of thrombosis and haemostasis, 2012-09, Vol.10 (9), p.1792-1801

2012

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Extended half‐life pegylated, full‐length recombinant factor VIII for prophylaxis in children with severe haemophilia A

Haemophilia : the official journal of the World Federation of Hemophilia, 2017-03, Vol.23 (2), p.238-246

2017

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The diagnosis and management of factor VIII and IX inhibitors: a guideline from the United Kingdom Haemophilia Centre Doctors Organisation

British journal of haematology, 2006-06, Vol.133 (6), p.591-605

2006

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Novel, human cell line-derived recombinant factor VIII (Human-cl rhFVIII, Nuwiq®) in children with severe haemophilia A: efficacy, safety and pharmacokinetics

Haemophilia : the official journal of the World Federation of Hemophilia, 2016-03, Vol.22 (2), p.232-239

2016

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Prospective observational cohort studies for studying rare diseases: the European PedNet Haemophilia Registry

Haemophilia : the official journal of the World Federation of Hemophilia, 2014-07, Vol.20 (4), p.e280-e286

2014

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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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Factors affecting the Haemophilia Joint Health Score in children with severe haemophilia

Haemophilia : the official journal of the World Federation of Hemophilia, 2013-07, Vol.19 (4), p.626-631

2013

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Mode of delivery in hemophilia: vaginal delivery and Cesarean section carry similar risks for intracranial hemorrhages and other major bleeds

Haematologica (Roma), 2019-10, Vol.104 (10), p.2100-2106

2019

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Plasma and albumin‐free recombinant factor VIII: pharmacokinetics, efficacy and safety in previously treated pediatric patients

Journal of thrombosis and haemostasis, 2008-08, Vol.6 (8), p.1319-1326

2008

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Cerebral venous sinus thrombosis in children: risk factors, presentation, diagnosis and outcome

Brain (London, England : 1878), 2005-03, Vol.128 (3), p.477-489

2005

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The haemtrack home therapy reporting system: Design, implementation, strengths and weaknesses: A report from UK Haemophilia Centre Doctors Organisation

Haemophilia : the official journal of the World Federation of Hemophilia, 2017-09, Vol.23 (5), p.728-735

2017

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Vaccinations are not associated with inhibitor development in boys with severe haemophilia A

Haemophilia : the official journal of the World Federation of Hemophilia, 2018-03, Vol.24 (2), p.283-290

2018

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Long‐term tolerability, immunogenicity and efficacy of Nuwiq® (human‐cl rhFVIII) in children with severe haemophilia A

Haemophilia : the official journal of the World Federation of Hemophilia, 2018-07, Vol.24 (4), p.595-603

2018

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How to achieve full prophylaxis in young boys with severe haemophilia A: different regimens and their effect on early bleeding and venous access

Haemophilia : the official journal of the World Federation of Hemophilia, 2015-07, Vol.21 (4), p.444-450

2015

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The incidence, risk and functional outcomes of intracranial haemorrhage in children with inherited bleeding disorders at one haemophilia center

Haemophilia : the official journal of the World Federation of Hemophilia, 2016-07, Vol.22 (4), p.556-563

2016

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First‐line immune tolerance induction for children with severe haemophilia A: A protocol from the UK Haemophilia Centre Doctors' Organisation Inhibitor and Paediatric Working Parties

Haemophilia : the official journal of the World Federation of Hemophilia, 2017-09, Vol.23 (5), p.654-659

2017

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Factor XIII – an under diagnosed deficiency – are we using the right assays?

Journal of thrombosis and haemostasis, 2010-11, Vol.8 (11), p.2478-2482

2010

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Using routine Haemophilia Joint Health Score for international comparisons of haemophilia outcome: standardization is needed

Haemophilia : the official journal of the World Federation of Hemophilia, 2016-01, Vol.22 (1), p.142-147

2016

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Transgenic cotton and sterile insect releases synergize eradication of pink bollworm a century after it invaded the United States

Proceedings of the National Academy of Sciences - PNAS, 2021-01, Vol.118 (1), p.1

2021

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Thrombophilia and first arterial ischaemic stroke: a systematic review

Archives of disease in childhood, 2005-04, Vol.90 (4), p.402-405

2005

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The incidence of factor VIII inhibitors in severe haemophilia A following a major switch from full-length to B-domain-deleted factor VIII: a prospective cohort comparison

Haemophilia : the official journal of the World Federation of Hemophilia, 2015-03, Vol.21 (2), p.219-226

2015

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Comment on: Interpreting data on inhibitor development from previously untreated patient studies, beware of premature conclusions

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

Prophylactic treatment of bleeding episodes in children <12 years with moderate to severe hereditary factor X deficiency (FXD): Efficacy and safety of a high‐purity plasma‐derived factor X (pdFX) concentrate

Treatment of bleeding episodes in haemophilia A complicated by a factor VIII inhibitor in patients receiving Emicizumab. Interim guidance from UKHCDO Inhibitor Working Party and Executive Committee

A phenotype–genotype correlation of ADAMTS13 mutations in congenital thrombotic thrombocytopenic purpura patients treated in the United Kingdom

Extended half‐life pegylated, full‐length recombinant factor VIII for prophylaxis in children with severe haemophilia A

The diagnosis and management of factor VIII and IX inhibitors: a guideline from the United Kingdom Haemophilia Centre Doctors Organisation

Novel, human cell line-derived recombinant factor VIII (Human-cl rhFVIII, Nuwiq®) in children with severe haemophilia A: efficacy, safety and pharmacokinetics

Prospective observational cohort studies for studying rare diseases: the European PedNet Haemophilia Registry

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

Factors affecting the Haemophilia Joint Health Score in children with severe haemophilia

Mode of delivery in hemophilia: vaginal delivery and Cesarean section carry similar risks for intracranial hemorrhages and other major bleeds

Plasma and albumin‐free recombinant factor VIII: pharmacokinetics, efficacy and safety in previously treated pediatric patients

Cerebral venous sinus thrombosis in children: risk factors, presentation, diagnosis and outcome

The haemtrack home therapy reporting system: Design, implementation, strengths and weaknesses: A report from UK Haemophilia Centre Doctors Organisation

Vaccinations are not associated with inhibitor development in boys with severe haemophilia A

Long‐term tolerability, immunogenicity and efficacy of Nuwiq® (human‐cl rhFVIII) in children with severe haemophilia A

How to achieve full prophylaxis in young boys with severe haemophilia A: different regimens and their effect on early bleeding and venous access

The incidence, risk and functional outcomes of intracranial haemorrhage in children with inherited bleeding disorders at one haemophilia center

First‐line immune tolerance induction for children with severe haemophilia A: A protocol from the UK Haemophilia Centre Doctors' Organisation Inhibitor and Paediatric Working Parties

Factor XIII – an under diagnosed deficiency – are we using the right assays?

Using routine Haemophilia Joint Health Score for international comparisons of haemophilia outcome: standardization is needed

Transgenic cotton and sterile insect releases synergize eradication of pink bollworm a century after it invaded the United States

Thrombophilia and first arterial ischaemic stroke: a systematic review

The incidence of factor VIII inhibitors in severe haemophilia A following a major switch from full-length to B-domain-deleted factor VIII: a prospective cohort comparison

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