J. Grabell

发表

Rapid Acquisition of Immunologic Tolerance to Factor VIII and Disappearance of Anti-factor VIII IgG4 After Prophylactic Therapy in a Hemophilia A Patient With High-titer Factor VIII Inhibitor

P. Moorehead, D. Lillicrap, Lisa Thibeault, 2015, Journal of pediatric hematology/oncology.

Quantitative and qualitative changes of von Willebrand factor and their impact on mortality in patients with end-stage kidney disease

P. James, R. Holden, A. Tuttle, 2013, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Aging and ABO blood type influence von Willebrand factor and factor VIII levels through interrelated mechanisms

P. James, W. Hopman, D. Lillicrap, 2016, Journal of thrombosis and haemostasis : JTH.

Generation and validation of the Condensed MCMDM‐1VWD Bleeding Questionnaire for von Willebrand disease

P. James, W. Hopman, D. Lillicrap, 2008, Journal of thrombosis and haemostasis : JTH.

Patients with aortic stenosis have von Willebrand factor abnormalities and increased proliferation of endothelial colony forming cells

R. Kloosterman, P. James, J. Grabell, 2019, Journal of thrombosis and haemostasis : JTH.

Relative contributions of bleeding scores and iron status on health‐related quality of life in von Willebrand disease: a cross‐sectional study

P. James, W. Hopman, J. Grabell, 2017, Haemophilia : the official journal of the World Federation of Hemophilia.

Quantification of perioperative changes in von Willebrand factor and factor VIII during elective orthopaedic surgery in normal individuals

W. Hopman, D. Lillicrap, A. Tuttle, 2013, Haemophilia : the official journal of the World Federation of Hemophilia.

Challenges and knowledge gaps facing hemophilia carriers today: Perspectives from patients and health care providers

W. Hopman, J. Grabell, P. James, 2022, Research and practice in thrombosis and haemostasis.

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

J. Mahlangu, P. James, W. Hopman, 2017, Haemophilia : the official journal of the World Federation of Hemophilia.

Obstetric bleeding among women with inherited bleeding disorders: a retrospective study

Graeme N. Smith, P. James, W. Hopman, 2016, Haemophilia : the official journal of the World Federation of Hemophilia.

Changes in von Willebrand factor level and von Willebrand activity with age in type 1 von Willebrand disease

P. James, D. Lillicrap, J. Grabell, 2015, Haemophilia : the official journal of the World Federation of Hemophilia.

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

J. Mahlangu, P. James, W. Hopman, 2016, Haemophilia : the official journal of the World Federation of Hemophilia.

A decreased and less sustained desmopressin response in hemophilia A carriers contributes to bleeding.

P. James, W. Hopman, R. Sidonio, 2018, Blood advances.

Let's Talk Period! Preliminary results of an online bleeding awareness knowledge translation project and bleeding assessment tool promoted on social media

P. James, J. Grabell, E. Reynen, 2017, Haemophilia : the official journal of the World Federation of Hemophilia.

Generation and optimization of the self‐administered bleeding assessment tool and its validation as a screening test for von Willebrand disease

P. James, W. Hopman, A. Tuttle, 2013, Haemophilia : the official journal of the World Federation of Hemophilia.

Normal range of bleeding scores for the ISTH‐BAT: adult and pediatric data from the merging project

Shamim A. Mollah, B. Coller, R. Montgomery, 2014, Haemophilia : the official journal of the World Federation of Hemophilia.

Bleeding assessment tools to predict von Willebrand disease: Utility of individual bleeding symptoms

A. Paterson, Yupu Liang, B. Coller, 2019, Research and practice in thrombosis and haemostasis.

Generation and optimization of the self‐administered pediatric bleeding questionnaire and its validation as a screening tool for von Willebrand disease

V. Blanchette, P. Moorehead, R. Klaassen, 2017, Pediatric blood & cancer.

Novel AMPA receptor potentiators LY392098 and LY404187: effects on recombinant human AMPA receptors in vitro

P. Ornstein, D. Bleakman, D. Zimmerman, 2001, Neuropharmacology.

A decreased and less sustained response to surrogates of haemostatic stress correlates with bleeding in type 1 von Willebrand disease

R. Kloosterman, W. Hopman, Lisa Thibeault, 2022, Haemophilia : the official journal of the World Federation of Hemophilia.

von Willebrand factor propeptide variants lead to impaired storage and ER retention in patient‐derived endothelial colony‐forming cells

A. Iorio, D. Lillicrap, A. Tuttle, 2022, Journal of thrombosis and haemostasis : JTH.

Acute pharmacological modulation of mGluR8 reduces measures of anxiety

R. Duvoisin, J. Raber, Dean G. Brown, 2010, Behavioural Brain Research.

Longitudinal bleeding assessment in von Willebrand disease utilizing an interim bleeding score

R. Montgomery, P. Christopherson, P. James, 2022, Journal of thrombosis and haemostasis : JTH.

Evaluating the effectiveness of let’s talk period’s high school educational outreach program: A pilot study

P. James, W. Hopman, Lisa Thibeault, 2021, Haemophilia.

Validation of the school age self‐administered pediatric bleeding questionnaire (Self‐PBQ) in children aged 8–12 years

V. Blanchette, N. Barrowman, R. Klaassen, 2019, Pediatric blood & cancer.

A transcriptome analysis of basal and stimulated VWF release from endothelial cells derived from patients with type 1 VWD

Charles T. Hindmarch, P. James, N. Renwick, 2022, Blood advances.

Generation and validation of the Condensed MCMDM‐1VWD Bleeding Questionnaire for von Willebrand disease

P. James, W. Hopman, D. Lillicrap, 2008, Journal of thrombosis and haemostasis : JTH.

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

P. Holme, J. Grabell, M. Mingot-Castellano, 2016, Haemophilia : the official journal of the World Federation of Hemophilia.

The bleeding score: Useful in predicting spontaneous bleeding events in adults with bleeding of unknown cause?

W. Hopman, J. Grabell, P. James, 2020, Haemophilia : the official journal of the World Federation of Hemophilia.