Short-term eltrombopag for surgical preparation of a patient with inherited thrombocytopenia deriving from MYH9 mutation
Author:
Publisher
Georg Thieme Verlag KG
Subject
Hematology
Link
http://www.thieme-connect.de/products/ejournals/pdf/10.1160/TH12-01-0005.pdf
Reference12 articles.
1. Diagnosis and Management of Inherited Platelet Disorders
2. Recent advances in the understanding and management of MYH9-related inherited thrombocytopenias
3. Advances in the understanding of MYH9 disorders
4. Heavy chain myosin 9-related disease (MYH9-RD): Neutrophil inclusions of myosin-9 as a pathognomonic sign of the disorder
5. Intriguing outcome of JAK2V617F mutation seen in a patient with MYH9-related hereditary macrothrombocytopenia
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1. MYH9-related inherited thrombocytopenia: the genetic spectrum, underlying mechanisms, clinical phenotypes, diagnosis, and management approaches;Research and Practice in Thrombosis and Haemostasis;2024-08
2. Update on the Use of Thrombopoietin-Receptor Agonists in Pediatrics;Hämostaseologie;2024-06-26
3. Anaesthesia recommendations for MYH9-related disease (MYH9-RD);ANASTH INTENSIVMED;2023
4. “MYH9 mutation and squamous cell cancer of the tongue in a young adult: a novel case report”;Diagnostic Pathology;2022-02-06
5. A thrombopoietin receptor agonist to rescue an unusual platelet transfusion-induced reaction in a p.V1316M-associated von Willebrand disease type 2B patient;Therapeutic Advances in Hematology;2022-01
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