The ITP syndrome: pathogenic and clinical diversity.

By D. Cines, J. Bussel, H. Liebman, E. L. Luning Prak. Blood, 2009

801 citations recorded by the source corpus.

Subfields: Hematology, Pathology and Forensic Medicine

View Paper: https://www.semanticscholar.org/paper/8f59a352efd1ed98f1c64c2911e8ac2651db6f05

Citations in the corpus

• American Society of Hematology 2019 guidelines for immune thrombocytopenia. (2019, neutral): “ITP is a heterogeneous disorder with variable clinical symptoms and remains a diagnosis of exclusion of other causes of thrombocytopenia.(17) The likelihood of a spontaneous remission from ITP is age related, with 1-year remission rates of 74% in children ,1 year of age, 67% in those between 1 and 6”