Search Results - "Lim, Ming Y"
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1
Leukocytoclastic vasculitis in T‐cell lymphoma
Published in Clinical case reports (01-12-2020)“…This case highlights the importance of looking for an occult malignancy when LCV is diagnosed clinically without any other signs suggestive of an infectious or…”
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2
An Unusual Case of Hyperhemolysis Syndrome and Delayed Hemolytic Transfusion Reaction due to Anti-Jk(a) and Anti-P1 Antibodies
Published in Case reports in medicine (31-12-2023)“…Background. Hyperhemolysis syndrome (HS) is a severe hemolytic transfusion reaction that can cause hemoglobin and hematocrit levels to drop below…”
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3
Acquired von Willebrand syndrome in monoclonal gammopathy – A scoping review on hemostatic management
Published in Research and practice in thrombosis and haemostasis (01-02-2021)“…Acquired von Willebrand syndrome (AVWS) has been associated with monoclonal gammopathy of undetermined significance (MGUS), with limited data on its…”
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4
Parvovirus B19‐induced hemophagocytic lymphohistiocytosis: Case report and review of the literature
Published in Clinical case reports (01-11-2019)“…HLH is a catastrophic and likely underdiagnosed pathology with multiple triggers including infection. PVB19 can cause persistent marrow infection leading to…”
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5
Successful Management of Thrombotic Thrombocytopenic Purpura in a Jehovah’s Witness: An Individualized Approach With Joint Decision-Making
Published in Journal of patient experience (01-02-2020)“…The management of thrombotic thrombocytopenic purpura (TTP) presents a unique challenge in individuals who are unable to accept plasma due to religious…”
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6
Outcomes of Using IVC Filters in Patients with Malignancy at an Academic Medical Center
Published in TH open : companion journal to thrombosis and haemostasis (01-04-2019)“…Systemic anticoagulation is regarded as optimal treatment and prophylaxis of venous thromboembolism (VTE). In malignancy, bleeding risk is increased while the…”
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7
Double-heterozygous FVL/PTGM: double the trouble
Published in Blood (06-06-2024)Get full text
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8
Spontaneous Heparin-Induced Thrombocytopenia and Venous Thromboembolism following Total Knee Arthroplasty
Published in Case reports in hematology (01-01-2017)“…A 72-year-old Caucasian woman was admitted for an elective left total knee arthroplasty. Her surgery was uncomplicated and she was discharged to a…”
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9
How do we optimally utilize factor concentrates in persons with hemophilia?
Published in Hematology (10-12-2021)“…The current mainstay of therapy for hemophilia is to replace the deficient clotting factor with the intravenous administration of exogenous clotting factor…”
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10
Left atrial appendage occlusion for management of atrial fibrillation in persons with hemophilia
Published in Thrombosis research (01-10-2021)“…•Management of atrial fibrillation (AF) is challenging in persons with hemophilia.•Left atrial appendage occlusion (LAAO) is an alternative option.•Hemostatic…”
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11
How I diagnose and treat antiphospholipid syndrome in pregnancy
Published in Blood (29-02-2024)“…[Display omitted] Antiphospholipid syndrome (APS) is a rare autoimmune disease characterized by arterial, venous, or microvascular thrombosis, pregnancy…”
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Prolonged Remission of Cancer of Unknown Primary following Initiation of Eculizumab Therapy for Paroxysmal Nocturnal Hemoglobinuria
Published in Case reports in hematology (01-01-2019)“…We report the case of a 64-year-old woman who presented with cancer of unknown primary treated with carboplatin and paclitaxel, followed by maintenance…”
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13
Differentiating and Managing Rare Thrombotic Microangiopathies During Pregnancy and Postpartum
Published in Obstetrics and gynecology (New York. 1953) (01-01-2023)“…The most common thrombotic microangiopathy (TMA) of pregnancy is the well-recognized syndrome of preeclampsia with hemolysis, elevated liver enzymes, and low…”
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14
Importance of pharmacokinetic studies in the management of acquired factor X deficiency
Published in European journal of haematology (01-01-2016)“…Up to 14% of individuals with systemic AL amyloidosis develop acquired factor X deficiency, which occurs due to adsorption of factor X onto amyloid fibrils…”
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15
Evidence-Based Minireview: For overweight or obese persons with hemophilia A, should factor VIII dosing be based on ideal or actual body weight?
Published in Hematology (10-12-2021)Get full text
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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
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-01-2022)“…Introduction Since the approval of emicizumab, a bispecific, factor VIII‐mimetic antibody, for use in persons with congenital haemophilia A in 2018, there have…”
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17
65-Year-Old Woman With Shortness of Breath and Dark Urine
Published in Mayo Clinic proceedings (01-09-2011)Get full text
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18
Update on Guidelines for the Prevention of Cancer-Associated Thrombosis
Published in Journal of the National Comprehensive Cancer Network (21-06-2022)“…Patients with cancer are at high risk of developing arterial and venous thromboembolism (VTE). They constitute 15% to 20% of the patients diagnosed with VTE…”
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Evaluation of ISTH-BAT as a predictor for factor deficiency in haemophilia carriers: a single-centre experience
Published in Blood coagulation & fibrinolysis (01-12-2021)Get full text
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20
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
Published in Journal of thrombosis and haemostasis (11-09-2024)“…People with bleeding disorders (PWBD) have been exposed to the risk of developing chronic viral hepatitis and cirrhosis after replacement therapy. Today, the…”
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