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Leukocytoclastic vasculitis in T‐cell lymphoma

Clinical case reports, 2020-12, Vol.8 (12), p.3630-3631

Lim, Ming Y.

2020

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An Unusual Case of Hyperhemolysis Syndrome and Delayed Hemolytic Transfusion Reaction due to Anti-Jk(a) and Anti-P1 Antibodies

Case reports in medicine, 2023-12, Vol.2023, p.5290115-5

2023

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Acquired von Willebrand syndrome in monoclonal gammopathy – A scoping review on hemostatic management

Research and practice in thrombosis and haemostasis, 2021-02, Vol.5 (2), p.356-365

2021

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How do we optimally utilize factor concentrates in persons with hemophilia?

Hematology, 2021-12, Vol.2021 (1), p.206-214

Lim, Ming Y

2021

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Left atrial appendage occlusion for management of atrial fibrillation in persons with hemophilia

Thrombosis research, 2021-10, Vol.206, p.9-13

2021

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Outcomes of Using IVC Filters in Patients with Malignancy at an Academic Medical Center

TH open : companion journal to thrombosis and haemostasis, 2019-04, Vol.3 (2), p.e117-e122

2019

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How I diagnose and treat antiphospholipid syndrome in pregnancy

Blood, 2024-02, Vol.143 (9), p.757-768

2024

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Parvovirus B19‐induced hemophagocytic lymphohistiocytosis: Case report and review of the literature

Clinical case reports, 2019-11, Vol.7 (11), p.2076-2081

2019

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Successful Management of Thrombotic Thrombocytopenic Purpura in a Jehovah’s Witness: An Individualized Approach With Joint Decision-Making

Journal of patient experience, 2020-02, Vol.7 (1), p.8-11

2020

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Differentiating and Managing Rare Thrombotic Microangiopathies During Pregnancy and Postpartum

Obstetrics and gynecology (New York. 1953), 2023-01, Vol.141 (1), p.85

2023

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Spontaneous Heparin-Induced Thrombocytopenia and Venous Thromboembolism following Total Knee Arthroplasty

Case reports in hematology, 2017-01, Vol.2017 (2017), p.1-4

2017

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Evidence-Based Minireview: For overweight or obese persons with hemophilia A, should factor VIII dosing be based on ideal or actual body weight?

Hematology, 2021-12, Vol.2021 (1), p.215-218

2021

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Off‐label use of emicizumab in persons with acquired haemophilia A and von Willebrand disease: A scoping review of the literature

Haemophilia : the official journal of the World Federation of Hemophilia, 2022-01, Vol.28 (1), p.4-17

2022

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Prolonged Remission of Cancer of Unknown Primary following Initiation of Eculizumab Therapy for Paroxysmal Nocturnal Hemoglobinuria

Case reports in hematology, 2019-01, Vol.2019 (2019), p.1-3

2019

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Importance of pharmacokinetic studies in the management of acquired factor X deficiency

European journal of haematology, 2016-01, Vol.96 (1), p.60-64

2016

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Evaluation of ISTH-BAT as a predictor for factor deficiency in haemophilia carriers: a single-centre experience

Blood coagulation & fibrinolysis, 2021-12, Vol.32 (8), p.611-613

2021

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The management of liver disease in people with congenital bleeding disorders: guidance from European Association for Haemophilia and Allied Disorders, European Haemophilia Consortium, ISTH, and World Federation of Hemophilia

Journal of thrombosis and haemostasis, 2024-09

2024

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Update on Guidelines for the Prevention of Cancer-Associated Thrombosis

Journal of the National Comprehensive Cancer Network, 2022-06, Vol.20 (13), p.1-8

2022

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Limited impact of clinician education on reducing inappropriate PF4 testing for heparin-induced thrombocytopenia

Journal of thrombosis and thrombolysis, 2019-02, Vol.47 (2), p.287-291

2019

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Targeting a higher plasma VWF level at time of delivery in pregnant individuals with von Willebrand disease: Outcomes at a single‐institution cohort study

Haemophilia : the official journal of the World Federation of Hemophilia, 2024-03, Vol.30 (2), p.470-477

2024

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Perioperative Recommendations for Corneal Refractive Surgery Patients With Inherited Bleeding Disorders

Cornea, 2024-07

2024

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Concomitant use of combined hormonal contraceptives and antifibrinolytic agents for the management of heavy menstrual bleeding: A practice pattern survey

Thrombosis research, 2021-08, Vol.204, p.95-100

2021

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Characteristics and outcomes of patients on concurrent direct oral anticoagulants and targeted anticancer therapies—TacDOAC registry: Communication from the ISTH SSC Subcommittee on Hemostasis and Malignancy

Journal of thrombosis and haemostasis, 2021-08, Vol.19 (8), p.2068-2081

2021

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Nonsevere hemophilia A: often overlooked, but not forgotten

Current opinion in hematology, 2020-09, Vol.27 (5), p.295-301

2020

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Vaccine‐induced thrombotic thrombocytopenia following Ad26.COV2.S vaccine in a man presenting as acute venous thromboembolism

American journal of hematology, 2021-09, Vol.96 (9), p.E346-E349

2021

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Leukocytoclastic vasculitis in T‐cell lymphoma

An Unusual Case of Hyperhemolysis Syndrome and Delayed Hemolytic Transfusion Reaction due to Anti-Jk(a) and Anti-P1 Antibodies

Acquired von Willebrand syndrome in monoclonal gammopathy – A scoping review on hemostatic management

How do we optimally utilize factor concentrates in persons with hemophilia?

Left atrial appendage occlusion for management of atrial fibrillation in persons with hemophilia

Outcomes of Using IVC Filters in Patients with Malignancy at an Academic Medical Center

How I diagnose and treat antiphospholipid syndrome in pregnancy

Parvovirus B19‐induced hemophagocytic lymphohistiocytosis: Case report and review of the literature

Successful Management of Thrombotic Thrombocytopenic Purpura in a Jehovah’s Witness: An Individualized Approach With Joint Decision-Making

Differentiating and Managing Rare Thrombotic Microangiopathies During Pregnancy and Postpartum

Spontaneous Heparin-Induced Thrombocytopenia and Venous Thromboembolism following Total Knee Arthroplasty

Evidence-Based Minireview: For overweight or obese persons with hemophilia A, should factor VIII dosing be based on ideal or actual body weight?

Off‐label use of emicizumab in persons with acquired haemophilia A and von Willebrand disease: A scoping review of the literature

Prolonged Remission of Cancer of Unknown Primary following Initiation of Eculizumab Therapy for Paroxysmal Nocturnal Hemoglobinuria

Importance of pharmacokinetic studies in the management of acquired factor X deficiency

Evaluation of ISTH-BAT as a predictor for factor deficiency in haemophilia carriers: a single-centre experience

The management of liver disease in people with congenital bleeding disorders: guidance from European Association for Haemophilia and Allied Disorders, European Haemophilia Consortium, ISTH, and World Federation of Hemophilia

Update on Guidelines for the Prevention of Cancer-Associated Thrombosis

Limited impact of clinician education on reducing inappropriate PF4 testing for heparin-induced thrombocytopenia

Targeting a higher plasma VWF level at time of delivery in pregnant individuals with von Willebrand disease: Outcomes at a single‐institution cohort study

Perioperative Recommendations for Corneal Refractive Surgery Patients With Inherited Bleeding Disorders

Concomitant use of combined hormonal contraceptives and antifibrinolytic agents for the management of heavy menstrual bleeding: A practice pattern survey

Characteristics and outcomes of patients on concurrent direct oral anticoagulants and targeted anticancer therapies—TacDOAC registry: Communication from the ISTH SSC Subcommittee on Hemostasis and Malignancy

Nonsevere hemophilia A: often overlooked, but not forgotten

Vaccine‐induced thrombotic thrombocytopenia following Ad26.COV2.S vaccine in a man presenting as acute venous thromboembolism

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