Diagnosis and management of acute graft-versus-host disease
Dignan, F. L., et al., Br J Haematol, 158: 30-45.
Dignan, F. L., et al., Br J Haematol, 158: 30-45.
Antithrombotic Therapy and Prevention of Thrombosis, 9th ed: American College of Chest Physicians Evidence-Based Clinical Practice Guidelines
CHEST 2012;
This guidance updates and replaces the previous guideline on the investigation and management of antiphospholipid syndrome (APS) published in
Aplastic anemia remains a diagnosis of exclusion. Our ability to reliably diagnose, and therefore exclude, a variety of
Autoimmune lymphoproliferative syndrome (ALPS) represents a failure of apoptotic mechanisms to maintain lymphocyte homeostasis, permitting accumulation of lymphoid
Guidelines on hereditary spherocytosis (HS) published in 2004 (Bolton-Maggs et al, 2004) are here replaced to reflect changes in current
Hemophagocytic lymphohistiocytosis (HLH) is a syndrome of pathologic immune activation, occurring as either a familial disorder or a
BLOOD, 13 OCTOBER 2011 , VOLUME 118, NUMBER 15
Richard L. Bakst, Martin S. Tallman, Dan Douer and Joachim Yahalom
Blood 2011 118:3785-3793
The purpose of this article is to set forth our approach to diagnosing and managing the
thalassemias, including b-thalassemia intermedia and
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