Clinical Features and Gene Mutation Analysis of Congenital Thrombotic Thrombocytopenic Purpura in Neonates
Author:
Publisher
Frontiers Media SA
Subject
Pediatrics, Perinatology and Child Health
Reference20 articles.
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3. Thrombotic thrombocytopenic purpura associated with von Willebrand factor-cleaving protease (ADAMTS13) deficiency in children;Loirat;Semin Thromb Hemost.,2006
4. Use of the ADAMTS13 activity assay improved the accuracy and efficiency of the diagnosis and treatment of suspected acquired thrombotic thrombocytopenic purpura;Barrows;Arch Pathol Lab Med.,2014
5. Congenital thrombotic thrombocytopenic purpura: Upshaw-Schulman syndrome: a cause of neonatal death and review of literature;Sharma;J Matern Fetal Neonatal Med.,2016
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1. Novel Molecular Therapies and Genetic Landscape in Selected Rare Diseases with Hematologic Manifestations: A Review of the Literature;Cells;2023-01-30
2. Early indicators of neonatal‐onset hereditary thrombotic thrombocytopenia purpura;Research and Practice in Thrombosis and Haemostasis;2022-10
3. Congenital thrombotic thrombocytopenic purpura simulating alloimmune thrombocytopenia;Journal of Clinical Neonatology;2022
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