N. O'Connell

发表

The current and future role of plasma-derived clotting factor concentrate in the treatment of haemophilia A.

B. Kevane, N. O'Connell, 2018, Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis.

Factor XI deficiency : a study of clinical, laboratory and molecular modifiers of bleeding phenotype

N. O'Connell, 2011 .

Recurrent lower limb venous thrombosis associated with a congenitally absent infrarenal inferior vena cava.

P. Beddy, N. O'Connell, J. O’Donnell, 2016, QJM : monthly journal of the Association of Physicians.

COVID19 coagulopathy in Caucasian patients

N. O'Connell, I. Martín-Loeches, C. Bergin, 2020, British journal of haematology.

Clinical conditions and patient factors significantly influence diagnostic utility of D-dimer in venous thromboembolism

N. O'Connell, M. Duggan, A. Qasim, 2009, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Oral rivaroxaban for pulmonary embolism.

N. O'Connell, J. O’Donnell, D. O’Donnell, 2012, The New England journal of medicine.

Increased galactose expression and enhanced clearance in patients with low von Willebrand factor.

Kenneth L. Jones, P. James, J. Di Paola, 2019, Blood.

Prevalence, causes, and characterization of factor XI inhibitors in patients with inherited factor XI deficiency.

D. Steinberg, Christine A. Lee, R. T. Sjin, 2003, Blood.

Significant gynecological bleeding in women with low von Willebrand factor levels.

P. James, J. Di Paola, N. O'Connell, 2018, Blood advances.

Novel insights into the clinical phenotype and pathophysiology underlying low VWF levels.

Kenneth L. Jones, P. James, J. Di Paola, 2017, Blood.

von Willebrand's disease: an important cause of dysfunctional uterine bleeding

Y. L. Woo, J. Bonnar, R. Corbally, 2002, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Recombinant factor VIIa to prevent surgical bleeding in factor XI deficiency

D. Perry, N. O'Connell, C. Lee, 2008, Haemophilia : the official journal of the World Federation of Hemophilia.

Guideline for the diagnosis and management of the rare coagulation disorders

A. Mumford, N. O'Connell, M. Mathias, 2014, British journal of haematology.

Vaccine‐induced immune thrombotic thrombocytopenia (VITT) – a novel clinico‐pathological entity with heterogeneous clinical presentations

G. Benson, D. O’Keeffe, N. O'Connell, 2021, British journal of haematology.

Out of Sight, out of Mind? An Audit Which Proposes a Follow-Up and Management Pathway for Inferior Vena Cava Filters

N. O'Connell, B. White, J. O'Donnell, 2016, Thrombosis.

Physical activity, physical fitness and cardiometabolic risk amongst adults with moderate and severe haemophilia

N. O'Connell, E. Singleton, J. O’Donnell, 2022, Haemophilia : the official journal of the World Federation of Hemophilia.

Recombinant factor VIIa in the management of surgery and acute bleeding episodes in children with haemophilia and high responding inhibitors

K. Khair, R. Liesner, N. O'Connell, 2002, Pathophysiology of haemostasis and thrombosis.

Factor XI deficiency--from molecular genetics to clinical management.

N. O'Connell, 2003, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Screening for factor XI deficiency amongst pregnant women of Ashkenazi Jewish origin

D. Economides, N. O'Connell, C. Lee, 2006, Haemophilia : the official journal of the World Federation of Hemophilia.

Recombinant factor IX‐Fc fusion protein in severe hemophilia B: Patient‐reported outcomes and health‐related quality of life

J. Mahlangu, N. O'Connell, E. Singleton, 2021, Research and practice in thrombosis and haemostasis.

Management of elective procedures in low von Willebrand factor patients in the LoVIC study

P. James, J. Di Paola, A. Dougall, 2020, Journal of thrombosis and haemostasis : JTH.

Analysis and results of the recombinant factor VIIa extended-use registry.

D. Perry, M. Laffan, D. O'shaughnessy, 2003, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Factor XI deficiency.

N. O'Connell, 2004, Seminars in hematology.

Vaccine-induced thrombosis and thrombocytopenia (VITT) in Ireland: A review of cases and current practices

D. O’Keeffe, N. O'Connell, Kanthi Perera, 2021, Thrombosis Update.

More on COVID‐19 coagulopathy in Caucasian patients

N. O'Connell, I. Martín-Loeches, C. Bergin, 2020, British journal of haematology.

Lenalidomide as a novel treatment for refractory acquired von Willebrand syndrome associated with monoclonal gammopathy

N. O'Connell, O. Rawley, J. O’Donnell, 2016, Journal of thrombosis and haemostasis : JTH.

Massive pseudotumour resection with recombinant  factor VIIa (NovoSeven) cover

N. O'Connell, O. Smith, M. Byrne, 2002, British journal of haematology.

Allogeneic Hematopoietic Stem Cell Transplantation for a BCR-FGFR1 Myeloproliferative Neoplasm Presenting as Acute Lymphoblastic Leukemia

S. Langabeer, K. Haslam, N. O'Connell, 2012, Case reports in hematology.

Fatal Pancreatic Necrosis after Pregnancy-Associated Thrombotic Thrombocytopenic Purpura

D. O’Briain, N. O'Connell, P. Browne, 2001, Hematology.

patients with inherited factor XI deficiency Prevalence, causes, and characterization of factor XI inhibitors in

M. Steinberg, Christine A. Lee, R. Loewenthal, 2013 .

Speaker Abstracts

N. O'Connell, K. Bartels, N. Larkin, 2011, Haemophilia.

Single centre, real‐world experience of perioperative rFIXFc use in adult patients with haemophilia B undergoing major and minor surgery

A. Dougall, N. O'Connell, E. Singleton, 2021, Haemophilia : the official journal of the World Federation of Hemophilia.

Telehealth for delivery of haemophilia comprehensive care during the COVID‐19 pandemic

A. Dougall, Laura Parkinson, N. O'Connell, 2020, Haemophilia : the official journal of the World Federation of Hemophilia.

A systematic review of physical activity in people with haemophilia and its relationship with bleeding phenotype and treatment regimen

N. O'Connell, P. Turecek, J. Gormley, 2021, Haemophilia : the official journal of the World Federation of Hemophilia.

Development and testing of the Satisfaction Questionnaire with Intravenous or Subcutaneous Hemophilia Injection and results from the Phase 3 HAVEN 3 study of emicizumab prophylaxis in persons with haemophilia A without FVIII inhibitors

C. Kempton, J. Mahlangu, N. O'Connell, 2021, Haemophilia : the official journal of the World Federation of Hemophilia.

Real‐world outcomes with recombinant factor IX Fc fusion protein (rFIXFc) prophylaxis: Longitudinal follow‐up in a national adult cohort

N. O'Connell, E. Singleton, J. O’Donnell, 2021, Haemophilia : the official journal of the World Federation of Hemophilia.

Changing paradigms of hemophilia care across larger specialized treatment centers in the European region

C. Hermans, N. O'Connell, J. Windyga, 2022, Therapeutic advances in hematology.

The Use of Recombinant Factor VIIa in Surgical Bleeding in Nonhemophiliac Patients

D. Perry, N. O'Connell, 2003 .

The value of autofluorescence as a diagnostic feature of acute promyelocytic leukemia.

N. O'Connell, E. Lawlor, P. Browne, 2006, Haematologica.

A role for intravenous immunoglobulin in the treatment of Acquired Von Willebrand Syndrome associated with IgM gammopathy

N. O'Connell, J. O’Donnell, M. Lavin, 2018, Haemophilia : the official journal of the World Federation of Hemophilia.

Recombinant FVIIa in the management of uncontrolled hemorrhage

D. Perry, N. O'Connell, O. Smith, 2003, Transfusion.

Acquired Factor Xiii Deficiency: An Uncommon But Easily Missed Cause Of Severe Bleeding

N. O'Connell, B. White, J. O’Donnell, 2018, Irish medical journal.

Management of combined factor V and factor VIII deficiency in pregnancy

D. O’Keeffe, N. O'Connell, B. White, 2019, Journal of Obstetrics and Gynaecology Research.

Reversal of warfarin anticoagulation using prothrombin complex concentrate at 25 IU kg−1: results of the RAPID study

D. O’Keeffe, N. O'Connell, L. Egan, 2017, Transfusion medicine.

Lessons Learned From a Case of Behcet’s Disease Presenting With Fever and Life-Threatening Venous Thromboembolism

N. O'Connell, R. Conway, P. Conlon, 2022, Cureus.

Heterogeneity in the half-life of factor VIII concentrate in patients with hemophilia A is due to variability in the clearance of endogenous von Willebrand factor.

J. Johnsen, P. Fallon, J. Di Paola, 2023, Journal of thrombosis and haemostasis : JTH.

Missed at first Glanz: Glanzmann thrombasthenia initially misdiagnosed as Von Willebrand Disease.

N. O'Connell, E. Singleton, J. O’Donnell, 2019, Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis.