Congenital thrombotic thrombocytopenic purpura: Upshaw–Schulman syndrome: a cause of neonatal death and review of literature
Author:
Publisher
Informa UK Limited
Subject
Obstetrics and Gynecology,Pediatrics, Perinatology and Child Health
Link
http://www.tandfonline.com/doi/pdf/10.3109/14767058.2015.1071789
Reference17 articles.
1. An acute febrile pleiochromic anemia with hyaline thrombosis of the terminal arterioles and capillaries
2. The incidence of thrombotic thrombocytopenic purpura-hemolytic uremic syndrome: all patients, idiopathic patients, and patients with severe ADAMTS-13 deficiency
3. Congenital Deficiency of a Factor in Normal Plasma That Reverses Microangiopathic Hemolysis and Thrombocytopenia
4. Von Willebrand factor, ADAMTS13, and thrombotic thrombocytopenic purpura
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1. Early indicators of neonatal‐onset hereditary thrombotic thrombocytopenia purpura;Research and Practice in Thrombosis and Haemostasis;2022-10
2. Novel ADAMTS13 mutation in a family with three recurrent neonatal deaths: a case report and literature review;Translational Pediatrics;2022-05
3. Morbidities and mortality in patients with hereditary thrombotic thrombocytopenic purpura;Blood Advances;2022-01-27
4. De Novo Mutation of the ADAMTS13 Gene with Mesenteric Ischemia in an Infant with Congenital Thrombotic Thrombocytopenic Purpura;Case Reports in Hematology;2021-07-06
5. Clinical Features and Gene Mutation Analysis of Congenital Thrombotic Thrombocytopenic Purpura in Neonates;Frontiers in Pediatrics;2020-09-22
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