Recommended management in pre-PMF
What is the recommended management of prefibrotic primary myelofibrosis (pre-PMF)?
What is the recommended management of prefibrotic primary myelofibrosis (pre-PMF)?
Do you use any questionnaires to assess bleeding symptoms?
Do you continue phlebotomy in patients with polycythemia vera (PV) who receive cytoreductive treatment?
Should each patient homozygous for mutation of the C282Y gene be diagnosed with hemochromatosis and treated with phlebotomy?
What is the best blood test to check if a patient has iron deficiency?
Does a negative genetic test (C282Y and H63D) result exclude hemochromatosis in a patient with transferrin saturation >45% and ferritin level >1000?
Are ferritin levels affected by age or some of the typical geriatric conditions?
How to approach the differential diagnosis of hyperferritinemia?
What diet, medication, and physical activity should be recommended to a patient with hemochromatosis?