Significant haemoglobinopathies: guidelines for screening and diagnosis
British Journal of Haematology, 149, 35–49, doi:10.1111/j.1365-2141.2009.08054.x
British Journal of Haematology, 149, 35–49, doi:10.1111/j.1365-2141.2009.08054.x
Endoscopic gastrointestinal workup fails to establish the cause of iron deficiency anemia (IDA) in a substantial proportion of patients. In patients
Paroxysmal nocturnal hemoglobinuria (PNH) is an acquired disorder of the hematopoietic stem cell that makes blood cells more
These guidelines were established and agreed upon by the EWOG-MDS HSCT Board during a Consensus Conference on October
The postthrombotic syndrome (PTS) is a chronic complication of deep vein thrombosis (DVT) that imposes significant morbidity, reduces
Myelodysplastic syndromes (MDSs) are clonal hematopoietic disorders characterized by peripheral cytopenia, ineffective hematopoiesis, and an increased risk of
Type 2B von Willebrand disease (VWD) is an inherited bleeding disorder caused by changes in von Willebrand factor (VWF)
Disseminated intravascular coagulation (DIC) is a condition characterized by systemic activation of coagulation, potentially leading to thrombotic obstruction of
Astute clinicians have reported familial clustering of myelodysplastic syndrome (MDS) and acute leukemia (AL; MDS/AL) for decades.1 These
The incidence of pediatric venous thromboembolism (VTE) has been increasing significantly over the past decade in part as a result
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