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Chronic pain in haemophilia: assessment and analgesic treatment
Chronic pain in haemophilia: assessment and analgesic treatment
People with haemophilia tend to experience pain from an early age because of venipuncture and hemart
Orthopedic surgical procedures in people with hemophilia
Orthopedic surgical procedures in people with hemophilia
People with hemophilia tend to develop joint lesions secondary to the recurrent hemarthroses typical
Hematological treatment and prophylaxis in patients with and without inhibitors
Hematological treatment and prophylaxis in patients with and without inhibitors
This document focuses on the hematological treatment and prophylaxis that should be indicated in thr
Individualizing primary prophylaxis in patients with hemophilia A and B, adherence and new products
Individualizing primary prophylaxis in patients with hemophilia A and B, adherence and new products
The purpose of prophylaxis in hemophilic patients is to prevent bleeding. The latest guidelines of t
Nonpharmacological treatment for coping with pain
Nonpharmacological treatment for coping with pain
Pain is one of the most common reasons for consultation and one of the most difficult tasks to handl
A contemporary approach to the musculoskeletal problems associated with hemophilia
A contemporary approach to the musculoskeletal problems associated with hemophilia
It is essential that joint bleeds be treated in a hematologically and orthopedically optimal manner
Disability and the social impact of hemophilia
Disability and the social impact of hemophilia
In addition to receiving the medical treatment they need, people with hemophilia or other coagulopat
Hemostatic cover in orthopedic surgery
Hemostatic cover in orthopedic surgery
Bleeding into joints, known as hemarthrosis, is the most common kind of bleeding experienced by pati
Obesity and physical exercise in hemophilia
Obesity and physical exercise in hemophilia
The new coagulation factors have made possible to increase the life expectancy of patients with hemo
Haemophilic arthropathy: basic protocols for clinical examination and imaging
Haemophilic arthropathy: basic protocols for clinical examination and imaging
In haemophilia, screening protocols in the prevention and treatment of common lesions still require
Foundations of hemophilia and epidemiology
Foundations of hemophilia and epidemiology
Hemophilia, a congenital coagulopathy characterized by a deficiency in coagulation factor VIII (hemo
Catastrophic antiphospholipid syndrome immediately after coronary angiography: the unexpected complication
Catastrophic antiphospholipid syndrome immediately after coronary angiography: the unexpected complication
A 44-year-old woman with obstetric antiphospholipid syndrome (APS) presented to our institution with
Role of tissue factor pathway inhibitor in hormone-induced venous thromboembolism
Role of tissue factor pathway inhibitor in hormone-induced venous thromboembolism
Exposure to higher levels of steroid hormones, like that in pregnancy or during combined hormonal co
Addressing the haemophilia healthcare crisis amidst Taliban rule: a call to action
Addressing the haemophilia healthcare crisis amidst Taliban rule: a call to action
aMedical Research Center, Kateb University bAfghanistan National Charity Organization for Special Diseases (A...
A 10-year Australian experience of rare intraabdominal venous thrombosis with comparison to deep vein thrombosis and pulmonary embolism
A 10-year Australian experience of rare intraabdominal venous thrombosis with comparison to deep vein thrombosis and pulmonary embolism
Objective Intra-abdominal venous thromboembolism is rare with heterogeneous management. We aim to
Direct oral anticoagulant adsorption and laboratory detection of lupus anticoagulant
Direct oral anticoagulant adsorption and laboratory detection of lupus anticoagulant
Direct oral anticoagulants (DOACs) interfere with many coagulation assays, mostly in lupus anticoagu
Endothelium-biomarkers for postthrombotic syndrome: a case–control study
Endothelium-biomarkers for postthrombotic syndrome: a case–control study
Background The postthrombotic syndrome (PTS) is a long-term complication of deep venous thrombosi
Limited sampling strategies for individualized BAX 855 prophylaxis in severe hemophilia A: in silico evaluation
Limited sampling strategies for individualized BAX 855 prophylaxis in severe hemophilia A: in silico evaluation
Objective Limited sampling strategies (LSS) lower the burden of pharmacokinetic (PK)-guided dosin
Comment on: coagulopathy following Crotaline snakebites in northeast Florida
Comment on: coagulopathy following Crotaline snakebites in northeast Florida
Division of Medical Toxicology, Department of Emergency Medicine, Washington University School of Medicine, St. Lou...
Excluding JAK2 V617F mutation analysis from the primary immune thrombocytopenia ‘diagnosis of exclusion’
Excluding JAK2 V617F mutation analysis from the primary immune thrombocytopenia ‘diagnosis of exclusion’
Cancer Molecular Diagnostics, St. James's Hospital, Dublin, Ireland Correspondence to Stephen E. Langabeer, P...
Phenotypic variation in severe hemophilia A is related to endogenous thrombin potential and plasma levels of factor VII
Phenotypic variation in severe hemophilia A is related to endogenous thrombin potential and plasma levels of factor VII
Hemophilia A is a bleeding disorder caused by deficiency or low activity of circulating factor VIII
Venous thromboembolism in pediatric inflammatory bowel disease: an 11-year population-based nested case–control study in Canada
Venous thromboembolism in pediatric inflammatory bowel disease: an 11-year population-based nested case–control study in Canada
To investigate the occurrence of venous thromboembolism (VTE), clinical characteristics, risk factor
Characterization of thrombophilia-related plasmas evaluated by anticoagulants-mediated thrombin and plasmin generation assays
Characterization of thrombophilia-related plasmas evaluated by anticoagulants-mediated thrombin and plasmin generation assays
Disturbances in the balance between coagulation, anticoagulation and fibrinolysis may lead to thromb
The coexistence of antiβ2 glycoprotein 1 antibody antibody has no effect on hemophilia A patient
The coexistence of antiβ2 glycoprotein 1 antibody antibody has no effect on hemophilia A patient
National Clinical Research Center for Hematologic Diseases, Jiangsu Institute of Hematology, The First Affiliated H...
Molecular heterogeneity of factor XI deficiency in Tunisia
Molecular heterogeneity of factor XI deficiency in Tunisia
Factor XI (FXI) deficiency is a rare inherited bleeding disorder that is highly prevalent in Ashkena
A novel F13A1 gene mutation (Arg208Pro) in a Chinese patient with factor XIII deficiency
A novel F13A1 gene mutation (Arg208Pro) in a Chinese patient with factor XIII deficiency
The objective of the study was to analyse a novel F13A1 gene mutation in a Chinese patient with fact
Primary immune thrombocytopenia: a ‘diagnosis of exclusion’?
Primary immune thrombocytopenia: a ‘diagnosis of exclusion’?
Current diagnosis of primary immune thrombocytopenia (ITP) is presumptive, centered on excluding oth
Evaluation of coagulation parameters and impact of transfusion on coagulation in patients with beta thalassemia major
Evaluation of coagulation parameters and impact of transfusion on coagulation in patients with beta thalassemia major
There have been several studies that have shown that patients with beta thalassemia major are at a h
Epidemiological study about the mental state of patients after a pulmonary embolism or deep venous thrombosis event
Epidemiological study about the mental state of patients after a pulmonary embolism or deep venous thrombosis event
Venous thromboembolism (VTE) occurs frequently and represents a serious threat to patient health. Ho
Characterization of zebrafish gp1ba mutant and modelling Bernard Soulier syndrome
Characterization of zebrafish gp1ba mutant and modelling Bernard Soulier syndrome
The aim of this study is to model classical Bernard Soulier Syndrome in the zebrafish by targeting G
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