Upshaw-Schulman Syndrome With c.2728C>T Mutation in ADAMTS13 Gene
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Oncology,Hematology,Pediatrics, Perinatology and Child Health
Reference23 articles.
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2. Thrombotic thrombocytopenic purpura related to severe ADAMTS13 deficiency in children;Loirat;Pediatr Nephrol,2009
3. Studies on thrombopoiesis. I. A factor in normal human plasma required for platelet production; chronic thrombocytopenia due to its deficiency;Schulman;Blood,1960
4. Congenital deficiency of a factor in normal plasma that reverses microangiopathic hemolysis and thrombocytopenia;Upshaw;N Engl J Med,1978
5. Thrombocytopenia and severe hyperbilirubinemia in the neonatal period secondary to congenital thrombotic thrombocytopenic purpura and ADAMTS13 deficiency;Schiff;J Pediatr Hematol Oncol,2004
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Upshaw–Schulman Syndrome with a Novel Deletion in Exon 17 of ADAMTS 13 Gene;Indian Journal of Pediatrics;2022-01-23
2. Bilateral Ischemic Retinopathy Associated With Upshaw-Schulman Syndrome: A Case Report;Journal of VitreoRetinal Diseases;2021-10-21
3. Congenital Thrombotic Thrombocytopenic Purpura With a Novel ADAMTS13 Gene Mutation;Cureus;2020-12-13
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