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Classification of rare bleeding disorders (RBDs) based on the association between coagulant factor activity and clinical bleeding severity

Journal of thrombosis and haemostasis, 2012-09, Vol.10 (9), p.1938-1943

2012

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Serious hazards of transfusion – conference report: celebration of 20 years of UK haemovigilance

Transfusion medicine (Oxford, England), 2017-12, Vol.27 (6), p.393-400

Bolton‐Maggs, P. H. B.

2017

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SHOT conference report 2016: serious hazards of transfusion - human factors continue to cause most transfusion-related incidents

Transfusion medicine (Oxford, England), 2016-12, Vol.26 (6), p.401-405

Bolton-Maggs, P. H. B.

2016

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Guidelines for the use of fresh‐frozen plasma, cryoprecipitate and cryosupernatant

British journal of haematology, 2004-07, Vol.126 (1), p.11-28

2004

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Conference report: International Haemovigilance Seminar and the SHOT Annual Symposium, 10–12 July 2018

Transfusion medicine (Oxford, England), 2019-08, Vol.29 (4), p.247-252

Bolton‐Maggs, P.H.B.

2019

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The natural history of occult or angiodysplastic gastrointestinal bleeding in von Willebrand disease

Haemophilia : the official journal of the World Federation of Hemophilia, 2015-05, Vol.21 (3), p.338-342

2015

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A study of variations in the reported haemophilia A prevalence around the world

Haemophilia : the official journal of the World Federation of Hemophilia, 2010-01, Vol.16 (1), p.20-32

2010

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Factor XI deficiency

Haemophilia : the official journal of the World Federation of Hemophilia, 2008-11, Vol.14 (6), p.1183-1189

2008

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A study of variations in the reported haemophilia B prevalence around the world

Haemophilia : the official journal of the World Federation of Hemophilia, 2012-05, Vol.18 (3), p.e91-e94

2012

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Conference report: the 2015 SHOT symposium and report - what's new?

Transfusion medicine (Oxford, England), 2015-10, Vol.25 (5), p.295-298

Bolton-Maggs, P. H. B.

2015

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Pregnancy and rare bleeding disorders

Haemophilia : the official journal of the World Federation of Hemophilia, 2009-09, Vol.15 (5), p.990-1005

2009

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Evaluation of the use of global haemostasis assays to monitor treatment in factor XI deficiency

Haemophilia : the official journal of the World Federation of Hemophilia, 2017-03, Vol.23 (2), p.273-283

2017

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Factor XI-related thrombosis and the role of concentrate treatment in factor XI deficiency

Haemophilia : the official journal of the World Federation of Hemophilia, 2015-07, Vol.21 (4), p.477-480

2015

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Bullet points from SHOT: key messages and recommendations from the Annual SHOT Report 2013

Transfusion medicine (Oxford, England), 2014-08, Vol.24 (4), p.197-203

Bolton-Maggs, P. H. B.

2014

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Human errors in manual techniques for ABO/D grouping are associated with potentially lethal outcomes

Transfusion medicine (Oxford, England), 2019-08, Vol.29 (4), p.262-267

2019

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International haemovigilance: what have we learned and what do we need to do next?

Transfusion medicine (Oxford, England), 2019-08, Vol.29 (4), p.221-230

2019

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Guidelines for the diagnosis and management of hereditary spherocytosis

British journal of haematology, 2004-08, Vol.126 (4), p.455-474

2004

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The obstetric and gynaecological management of women with inherited bleeding disorders - review with guidelines produced by a taskforce of UK Haemophilia Centre Doctors' Organization

Haemophilia : the official journal of the World Federation of Hemophilia, 2006-07, Vol.12 (4), p.301-336

2006

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The administration of blood components: a British Society for Haematology Guideline

Transfusion medicine (Oxford, England), 2018-02, Vol.28 (1), p.3-21

2018

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The rare coagulation disorders - review with guidelines for management from the United Kingdom Haemophilia Centre Doctors' Organisation

Haemophilia : the official journal of the World Federation of Hemophilia, 2004-09, Vol.10 (5), p.593-628

2004

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FXI concentrate use and risk of thrombosis

Haemophilia : the official journal of the World Federation of Hemophilia, 2014-07, Vol.20 (4), p.e349-e351

2014

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Staffing in hospital transfusion laboratories: UKTLC surveys show cause for concern

Transfusion medicine (Oxford, England), 2019-04, Vol.29 (2), p.95-102

2019

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In vitro comparison of the effect of two factor XI (FXI) concentrates on thrombin generation in major FXI deficiency

Haemophilia : the official journal of the World Federation of Hemophilia, 2016-05, Vol.22 (3), p.403-410

2016

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Are the 'rules' for times in set up and duration of red cell transfusion too strict?

Transfusion medicine (Oxford, England), 2016-06, Vol.26 (3), p.166-169

2016

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Evaluation of the use of rotational thromboelastometry in the assessment of FXI deficency

Haemophilia : the official journal of the World Federation of Hemophilia, 2017-05, Vol.23 (3), p.449-457

2017

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Classification of rare bleeding disorders (RBDs) based on the association between coagulant factor activity and clinical bleeding severity

Serious hazards of transfusion – conference report: celebration of 20 years of UK haemovigilance

SHOT conference report 2016: serious hazards of transfusion - human factors continue to cause most transfusion-related incidents

Guidelines for the use of fresh‐frozen plasma, cryoprecipitate and cryosupernatant

Conference report: International Haemovigilance Seminar and the SHOT Annual Symposium, 10–12 July 2018

The natural history of occult or angiodysplastic gastrointestinal bleeding in von Willebrand disease

A study of variations in the reported haemophilia A prevalence around the world

Factor XI deficiency

A study of variations in the reported haemophilia B prevalence around the world

Conference report: the 2015 SHOT symposium and report - what's new?

Pregnancy and rare bleeding disorders

Evaluation of the use of global haemostasis assays to monitor treatment in factor XI deficiency

Factor XI-related thrombosis and the role of concentrate treatment in factor XI deficiency

Bullet points from SHOT: key messages and recommendations from the Annual SHOT Report 2013

Human errors in manual techniques for ABO/D grouping are associated with potentially lethal outcomes

International haemovigilance: what have we learned and what do we need to do next?

Guidelines for the diagnosis and management of hereditary spherocytosis

The obstetric and gynaecological management of women with inherited bleeding disorders - review with guidelines produced by a taskforce of UK Haemophilia Centre Doctors' Organization

The administration of blood components: a British Society for Haematology Guideline

The rare coagulation disorders - review with guidelines for management from the United Kingdom Haemophilia Centre Doctors' Organisation

FXI concentrate use and risk of thrombosis

Staffing in hospital transfusion laboratories: UKTLC surveys show cause for concern

In vitro comparison of the effect of two factor XI (FXI) concentrates on thrombin generation in major FXI deficiency

Are the 'rules' for times in set up and duration of red cell transfusion too strict?

Evaluation of the use of rotational thromboelastometry in the assessment of FXI deficency

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