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Evaluation of participants with suspected heritable platelet function disorders including recommendation and validation of a streamlined agonist panel

Blood, 2012-12, Vol.120 (25), p.5041-5049

2012

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Enrichment of FLI1 and RUNX1 mutations in families with excessive bleeding and platelet dense granule secretion defects

Blood, 2013-12, Vol.122 (25), p.4090-4093

2013

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A review of inherited platelet disorders with guidelines for their management on behalf of the UKHCDO

British journal of haematology, 2006-12, Vol.135 (5), p.603-633

2006

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Unique heterozygous intron 22 inversion band pattern in a haemophilic male detected by long polymerase chain reaction (PCR)

Thrombosis and haemostasis, 2008-04, Vol.99 (4), p.774-775

2008

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Identification and characterization of a novel P2Y12 variant in a patient diagnosed with type 1 von Willebrand disease in the European MCMDM-1VWD study

Blood, 2009-04, Vol.113 (17), p.4110-4113

2009

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A novel thromboxane A2 receptor N42S variant results in reduced surface expression and platelet dysfunction

Thrombosis and haemostasis, 2014, Vol.111 (5), p.923-932

2014

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Pregnancy in platelet-type VWD: a case series

Thrombosis and haemostasis, 2011-08, Vol.106 (2), p.386-387

2011

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Haemostatic problems in acute promyelocytic leukaemia

Blood reviews, 2006-11, Vol.20 (6), p.289-297

2006

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Von Willebrand disease

Clinical medicine (London, England), 2007-12, Vol.7 (6), p.629-632

Wilde, Jonathan T

2007

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Distinguishing between type 2B and pseudo‐von Willebrand disease and its clinical importance

British journal of haematology, 2006-06, Vol.133 (6), p.664-666

2006

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Elective surgery on factor VIII inhibitor patients using continuous infusion of recombinant activated factor VII: plasma factor VII activity of 10 IU/ml is associated with an increased incidence of bleeding

Thrombosis and haemostasis, 2001-10, Vol.86 (4), p.949-953

2001

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Inherited and de novo von Willebrand disease ‘Vicenza’ in UK families with the R1205H mutation: diagnostic pitfalls and new insights

British journal of haematology, 2006-10, Vol.135 (1), p.91-96

2006

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The incidence of lymphoma in the UK haemophilia population between 1978 and 1999

AIDS (London), 2002-09, Vol.16 (13), p.1803-1807

2002

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Demographic and clinical data in acquired hemophilia A: results from the European Acquired Haemophilia Registry (EACH2)

Journal of thrombosis and haemostasis, 2012-04, Vol.10 (4), p.622-631

2012

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Management of bleeding in acquired hemophilia A: results from the European Acquired Haemophilia (EACH2) Registry

Blood, 2012-07, Vol.120 (1), p.39-46

2012

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Immunosuppression for acquired hemophilia A: results from the European Acquired Haemophilia Registry (EACH2)

Blood, 2012-07, Vol.120 (1), p.47-55

2012

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Pregnancy-associated acquired haemophilia A: results from the European Acquired Haemophilia (EACH2) registry

BJOG : an international journal of obstetrics and gynaecology, 2012-11, Vol.119 (12), p.1529-1537

2012

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HIV and HCV coinfection in haemophilia

Haemophilia : the official journal of the World Federation of Hemophilia, 2004-01, Vol.10 (1), p.1-8

Wilde, J. T.

2004

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Characterization of multiple platelet activation pathways in patients with bleeding as a high-throughput screening option: use of 96-well Optimul assay

Blood, 2014-02, Vol.123 (8), p.e11-e22

2014

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The impact of HIV on mortality rates in the complete UK haemophilia population

AIDS (London), 2004-02, Vol.18 (3), p.525-533

2004

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Inhibitor development in non-severe haemophilia across Europe

Thrombosis and haemostasis, 2015-10, Vol.114 (4), p.670-675

2015

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Efficacy and safety of prophylaxis with once-weekly BAY 79-4980 compared with thrice-weekly rFVIII-FS in haemophilia A patients. A randomised, active-controlled, double-blind study

Thrombosis and haemostasis, 2012-11, Vol.108 (5), p.913-922

2012

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short report: Distinguishing between type 2B and pseudo-von Willebrand disease and its clinical importance

British journal of haematology, 2006-06, Vol.133 (6), p.664-666

2006

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FVIII inhibitor development according to concentrate: data from the EUHASS registry excluding overlap with other studies

Haemophilia : the official journal of the World Federation of Hemophilia, 2016-01, Vol.22 (1), p.e36-e38

2016

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Patient characteristics that influence efficacy of prophylaxis with rFVIII-FS three times per week: a subgroup analysis of the LIPLONG study

Haemophilia : the official journal of the World Federation of Hemophilia, 2014-05, Vol.20 (3), p.354-361

2014

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Evaluation of participants with suspected heritable platelet function disorders including recommendation and validation of a streamlined agonist panel

Enrichment of FLI1 and RUNX1 mutations in families with excessive bleeding and platelet dense granule secretion defects

A review of inherited platelet disorders with guidelines for their management on behalf of the UKHCDO

Unique heterozygous intron 22 inversion band pattern in a haemophilic male detected by long polymerase chain reaction (PCR)

Identification and characterization of a novel P2Y12 variant in a patient diagnosed with type 1 von Willebrand disease in the European MCMDM-1VWD study

A novel thromboxane A2 receptor N42S variant results in reduced surface expression and platelet dysfunction

Pregnancy in platelet-type VWD: a case series

Haemostatic problems in acute promyelocytic leukaemia

Von Willebrand disease

Distinguishing between type 2B and pseudo‐von Willebrand disease and its clinical importance

Elective surgery on factor VIII inhibitor patients using continuous infusion of recombinant activated factor VII: plasma factor VII activity of 10 IU/ml is associated with an increased incidence of bleeding

Inherited and de novo von Willebrand disease ‘Vicenza’ in UK families with the R1205H mutation: diagnostic pitfalls and new insights

The incidence of lymphoma in the UK haemophilia population between 1978 and 1999

Demographic and clinical data in acquired hemophilia A: results from the European Acquired Haemophilia Registry (EACH2)

Management of bleeding in acquired hemophilia A: results from the European Acquired Haemophilia (EACH2) Registry

Immunosuppression for acquired hemophilia A: results from the European Acquired Haemophilia Registry (EACH2)

Pregnancy-associated acquired haemophilia A: results from the European Acquired Haemophilia (EACH2) registry

HIV and HCV coinfection in haemophilia

Characterization of multiple platelet activation pathways in patients with bleeding as a high-throughput screening option: use of 96-well Optimul assay

The impact of HIV on mortality rates in the complete UK haemophilia population

Inhibitor development in non-severe haemophilia across Europe

Efficacy and safety of prophylaxis with once-weekly BAY 79-4980 compared with thrice-weekly rFVIII-FS in haemophilia A patients. A randomised, active-controlled, double-blind study

short report: Distinguishing between type 2B and pseudo-von Willebrand disease and its clinical importance

FVIII inhibitor development according to concentrate: data from the EUHASS registry excluding overlap with other studies

Patient characteristics that influence efficacy of prophylaxis with rFVIII-FS three times per week: a subgroup analysis of the LIPLONG study

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