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Updated: Mar 5, 2026

Continuous Manual Exchange Transfusion for Patients with Sickle Cell Disease: An Efficient Method to Avoid Iron Overload
Published on: March 14, 2017
Martin D Zielinski1, James R Stubbs, Kathleen S Berns
1From the Department of Surgery (M.D.Z., J.R.S.), Mayo Clinic, Rochester, Minnesota; Mayo Clinic Medical Transport (K.S.B., S.Z.), Rochester, Minnesota; Israel Defense Forces Medical Corps (E.G.), Haifa, Israel; Department of Surgery (A.D.M.), Allegheny General Hospital, Pittsburgh, Pennsylvania; Magen David Adom National Blood Services (E.S.), Israel; HEMS-Bergen, Emergency Medical Services Haukeland University Hospital (G.A.S.), Bergen, Norway; Institute of Cruise Ship Medicine (S.W.), Miami, Florida; The Institute for Transfusion Medicine (M.H.Y.), Pittsburgh, Pennsylvania; and the Department of Surgery (D.H.J.), University of Texas Health Sciences Center, San Antonio, Texas.
No abstract available in PubMed .
07:24A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy
11:59Detection of Residual Donor Erythroid Progenitor Cells after Hematopoietic Stem Cell Transplantation for Patients with Hemoglobinopathies
Published on: September 6, 2017