Search Results - "Al Arashi, Wala"
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Patient‐reported outcomes in autosomal inherited bleeding disorders: A systematic literature review
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-03-2022)“…Aim Currently, it is unknown which patient‐reported outcomes are important for patients with autosomal inherited bleeding disorders. Therefore, the purpose of…”
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Psychometrics of patient-reported outcomes measurement information system in von Willebrand disease, inherited platelet function disorders, and rare bleeding disorders
Published in Research and practice in thrombosis and haemostasis (01-05-2024)“…Patient-reported outcomes measurement information system (PROMIS) measures can be used to measure patient-reported outcomes. PROMIS measures, including…”
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Desmopressin testing in von Willebrand disease: Lowering the burden
Published in Research and practice in thrombosis and haemostasis (01-08-2022)“…Individuals with von Willebrand disease (VWD) require desmopressin testing because of interindividual response differences. However, testing is burdensome,…”
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Desmopressin to prevent and treat bleeding in pregnant women with an inherited bleeding disorder: a systematic literature review
Published in Journal of thrombosis and haemostasis (01-01-2024)“…Although desmopressin (DDAVP) is an accessible and inexpensive hemostatic drug, its use in pregnancy is still debated due to safety uncertainties. We aimed to…”
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Transcriptional and functional profiling identifies inflammation and endothelial-to-mesenchymal transition as potential drivers for phenotypic heterogeneity within a cohort of endothelial colony forming cells
Published in Journal of thrombosis and haemostasis (01-07-2024)“…Endothelial colony-forming cells (ECFCs) derived from patients can be used to investigate pathogenic mechanisms of vascular diseases like von Willebrand…”
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Functional characterization of a nanobody-based glycoprotein VI-specific platelet agonist
Published in Research and practice in thrombosis and haemostasis (01-10-2024)“…Glycoprotein (GP)VI is a platelet-specific collagen receptor required for platelet activation during hemostasis. Platelet reactivity toward collagen is…”
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Perioperative pharmacokinetic-guided factor VIII concentrate dosing in haemophilia (OPTI-CLOT trial): an open-label, multicentre, randomised, controlled trial
Published in The Lancet. Haematology (01-07-2021)“…Dosing of replacement therapy with factor VIII concentrate in patients with haemophilia A in the perioperative setting is challenging. Underdosing and…”
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A man who was unable to open his eyes
Published in Nederlands tijdschrift voor geneeskunde (21-06-2018)“…A 47-years-old man presented with the complaint that he could not open his eyes in the morning. Facial myxedema caused by hypothyroidism was evident. Pictures…”
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