Abstract
A thrombocytopenic state developing in the absence of any apparent underlying disorder and accompanied by an abundance of megakaryocytes in the bone marrow represents the syndrome of idiopathic thrombocytopenic purpura (ITP).
Cite
CITATION STYLE
APA
Shulman, N. R., Aster, R. H., Leitner, A., & Hiller, M. C. (1961). IMMUNOREACTIONS INVOLVING PLATELETS. V. POST-TRANSFUSION PURPURA DUE TO A COMPLEMENT-FIXING ANTIBODY AGAINST A GENETICALLY CONTROLLED PLATELET ANTIGEN. A PROPOSED MECHANISM FOR THROMBOCYTOPENIA AND ITS RELEVANCE IN “AUTOIMMUNITY”*. Journal of Clinical Investigation, 40(9), 1597–1620. https://doi.org/10.1172/jci104383
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.
Already have an account? Sign in
Sign up for free