P. Collins

发表

A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders.

Sri V. V. Deevi, W. Ouwehand, A. Attwood, 2016, Blood.

Successful engraftment of haploidentical stem cell transplant for familial haemophagocytic lymphohistiocytosis using both bone marrow and peripheral blood stem cells

P. Veys, M. Brocklesby, M. Watts, 1997, British journal of haematology.

Measurement of global haemostasis in severe haemophilia A following factor VIII infusion

P. Collins, E. Stephens, N. Macartney, 2007, British journal of haematology.

Communicating about haemophilia within the family: the importance of context and of experience

P. Atkinson, A. Clarke, P. Boddington, 2007, Haemophilia : the official journal of the World Federation of Hemophilia.

Management of von Willebrand disease: a guideline from the UK Haemophilia Centre Doctors' Organization

G. Dolan, M. Laffan, K. Pasi, 2004, Haemophilia : the official journal of the World Federation of Hemophilia.

Liver haemorrhage in haemophilia – a case report and review of the literature

P. Collins, M. Hamilton, W. French, 2006, Haemophilia : the official journal of the World Federation of Hemophilia.

Increased bleeding associated with protease inhibitor therapy in HIV‐positive patients with bleeding disorders

P. Giangrande, Christine A. Lee, C. Lee, 1999, British journal of haematology.

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

D. Perry, G. Dolan, A. Mumford, 2004, Haemophilia : the official journal of the World Federation of Hemophilia.

Inhibitor treatment in haemophilias A and B: summary statement for the 2006 international consensus conference

J. Astermark, J. Oldenburg, C. Leissinger, 2006, Haemophilia : the official journal of the World Federation of Hemophilia.

THE DIAGNOSIS and MANAGEMENT OF FACTOR VIII and IX INHIBITORS: A GUIDELINE FROM THE UK HAEMOPHILIA CENTRE DOCTORS' ORGANIZATION (UKHCDO)

D. Keeling, F. Hill, P. Collins, 2000, British journal of haematology.

Pharmacokinetics of Recombinant Factor VIII (Recombinate) Using One-stage Clotting and Chromogenic Factor VIII Assay

P. Giangrande, E. Gomperts, C. Hay, 1999, Thrombosis and Haemostasis.

Clinical evaluation of an advanced category antihaemophilic factor prepared using a plasma/albumin‐free method: pharmacokinetics, efficacy, and safety in previously treated patients with haemophilia A 1

A. Shapiro, M. Tarantino, C. Hay, 2004, Haemophilia : the official journal of the World Federation of Hemophilia.

Complications experienced with central venous catheters in children with congenital bleeding disorders

K. Khair, R. Liesner, P. Collins, 1997, British journal of haematology.

Pathogenesis of Thrombotic Complications of Haematological Malignancies.

P. Collins, 1996, Hematology.

The Diagnosis and Management of Factor VIII and IX Inhibitors : A Guideline from the United Kingdom Haemophilia Centre Doctors Organisation ( UKHCDO )

R. Liesner, D. Keeling, S. Brown, 2007 .

Case studies in therapeutics: warfarin resistance and inefficacy in a man with recurrent thromboembolism, and anticoagulant-associated priapism.

P. Routledge, P. Collins, J. White, 1998, British journal of clinical pharmacology.

Acquired hemophilia A: pathogenesis and treatment

P. Collins, Hea-Reung Park, 2012 .

Changing patterns of bleeding in patients with severe haemophilia A

G. Dolan, D. Stephensen, G. Dolan, 2009, Haemophilia : the official journal of the World Federation of Hemophilia.

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

R. Liesner, C. Hay, D. Keeling, 2006, British journal of haematology.

The incidence of factor VIII and factor IX inhibitors in the hemophilia population of the UK and their effect on subsequent mortality, 1977–99

S. Darby, D. Keeling, F. Hill, 2004, Journal of thrombosis and haemostasis : JTH.

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

R. Liesner, D. Hart, B. Palmer, 2015, Haemophilia : the official journal of the World Federation of Hemophilia.

R. Liesner, R. Liesner, T. Yee, 2011, Haemophilia : the official journal of the World Federation of Hemophilia.

20180829_A perioperative population PK model for FIX Population pharmacokinetics of factor IX in hemophilia B patients undergoing surgery Running head: Perioperative pharmacokinetics of factor IX

D. Hart, M. Cnossen, R. Liesner, 2022 .

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

G. Dolan, M. Scott, H. Xiang, 2017, Haemophilia : the official journal of the World Federation of Hemophilia.

Pharmacokinetic properties of IB1001, an investigational recombinant factor IX, in patients with haemophilia B: repeat pharmacokinetic evaluation and sialylation analysis

P. Mannucci, L. Valentino, M. Morfini, 2012, Haemophilia : the official journal of the World Federation of Hemophilia.

Selective angiographic embolization for recurrent elbow and knee haemarthroses in haemophilia: a retrospective case series

P. Collins, R. Alikhan, S. Obaji, 2015, Haemophilia : the official journal of the World Federation of Hemophilia.

Rituximab and immune tolerance in severe hemophilia A: a consecutive national cohort

R. Keenan, D. Perry, M. Laffan, 2009, Journal of thrombosis and haemostasis : JTH.

Insights into von Willebrand factor proteolysis: clinical implications

D. Bowen, P. Collins, P. Collins, 2006, British journal of haematology.

Increased clearance of von Willebrand factor antigen post‐DDAVP in Type 1 von Willebrand disease: is it a potential pathogenic process?

P. Collins, S. Brown, D. Bowen, 2003, Journal of thrombosis and haemostasis : JTH.

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

M. Makris, R. Liesner, D. Hart, 2017, Haemophilia : the official journal of the World Federation of Hemophilia.

A national survey of immunosuppression strategies for acquired haemophilia A

R. Liesner, P. Batty, D. Hart, 2015, Haemophilia.

Type 1 von Willebrand disease: application of emerging data to clinical practice

D. Lillicrap, P. Collins, A. Cumming, 2008, Haemophilia : the official journal of the World Federation of Hemophilia.