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PUBMED FOR HANDHELDS

Journal Abstract Search


580 related items for PubMed ID: 30265764

  • 21.
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  • 22. Hypoxic storage of donor red cells preserves deformability after exposure to plasma from adults with sickle cell disease.
    Karafin MS, Field JJ, Ilich A, Li L, Qaquish BF, Shevkoplyas SS, Yoshida T.
    Transfusion; 2023 Jan; 63(1):193-202. PubMed ID: 36310401
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  • 25. Plasma levels of sphingosine 1-phosphate are strongly correlated with haematocrit, but variably restored by red blood cell transfusions.
    Selim S, Sunkara M, Salous AK, Leung SW, Berdyshev EV, Bailey A, Campbell CL, Charnigo R, Morris AJ, Smyth SS.
    Clin Sci (Lond); 2011 Dec; 121(12):565-72. PubMed ID: 21749329
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  • 26. In vivo evaluation of the effect of sickle cell hemoglobin S, C and therapeutic transfusion on erythrocyte metabolism and cardiorenal dysfunction.
    D'Alessandro A, Nouraie SM, Zhang Y, Cendali F, Gamboni F, Reisz JA, Zhang X, Bartsch KW, Galbraith MD, Gordeuk VR, Gladwin MT.
    bioRxiv; 2023 Feb 14. PubMed ID: 36824724
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  • 28. Long-term cryopreservation of red cells from patients with sickle cell disease.
    Castro OL.
    Transfusion; 1985 Feb 14; 25(1):70-2. PubMed ID: 3969705
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  • 30. Red blood cell alloimmunization in sickle cell disease: assessment of transfusion protocols during two time periods.
    Campbell-Lee SA, Gvozdjan K, Choi KM, Chen YF, Saraf SL, Hsu LL, Gordeuk VR, Strauss RG, Triulzi DJ.
    Transfusion; 2018 Jul 14; 58(7):1588-1596. PubMed ID: 29570817
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  • 31. Delayed hemolytic transfusion reaction/hyperhemolysis syndrome in children with sickle cell disease.
    Talano JA, Hillery CA, Gottschall JL, Baylerian DM, Scott JP.
    Pediatrics; 2003 Jun 14; 111(6 Pt 1):e661-5. PubMed ID: 12777582
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  • 32. Routine storage of red blood cell (RBC) units in additive solution-3: a comprehensive investigation of the RBC metabolome.
    D'Alessandro A, Nemkov T, Kelher M, West FB, Schwindt RK, Banerjee A, Moore EE, Silliman CC, Hansen KC.
    Transfusion; 2015 Jun 14; 55(6):1155-68. PubMed ID: 25556331
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  • 34. The Unique Magnetic Signature of Sickle Red Blood Cells: A Comparison Between the Red Blood Cells of Transfused and Non-Transfused Sickle Cell Disease Patients and Healthy Donors.
    Weigand M, Gomez-Pastora J, Strayer J, Wu X, Choe H, Lu S, Plencner E, Landes K, Palmer A, Zborowski M, Desai P, Chalmers J.
    IEEE Trans Biomed Eng; 2022 Dec 14; 69(12):3582-3590. PubMed ID: 35544484
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  • 36. Hemoglobin A clearance in children with sickle cell anemia on chronic transfusion therapy.
    Yee MEM, Josephson CD, Winkler AM, Webb J, Luban NLC, Leong T, Stowell SR, Roback JD, Fasano RM.
    Transfusion; 2018 Jun 14; 58(6):1363-1371. PubMed ID: 29664198
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  • 38. Heterogeneity of blood processing and storage additives in different centers impacts stored red blood cell metabolism as much as storage time: lessons from REDS-III-Omics.
    D'Alessandro A, Culp-Hill R, Reisz JA, Anderson M, Fu X, Nemkov T, Gehrke S, Zheng C, Kanias T, Guo Y, Page G, Gladwin MT, Kleinman S, Lanteri M, Stone M, Busch M, Zimring JC, Recipient Epidemiology and Donor Evaluation Study-III (REDS-III).
    Transfusion; 2019 Jan 14; 59(1):89-100. PubMed ID: 30353560
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  • 39. Effect of Transfusion of Red Blood Cells With Longer vs Shorter Storage Duration on Elevated Blood Lactate Levels in Children With Severe Anemia: The TOTAL Randomized Clinical Trial.
    Dhabangi A, Ainomugisha B, Cserti-Gazdewich C, Ddungu H, Kyeyune D, Musisi E, Opoka R, Stowell CP, Dzik WH.
    JAMA; 2015 Dec 15; 314(23):2514-23. PubMed ID: 26637812
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