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Journal Abstract Search

129 related items for PubMed ID: 39373300

  • 41. Blood group genotyping in multi-transfused patients.
    Bakanay SM, Ozturk A, Ileri T, Ince E, Yavasoglu S, Akar N, Uysal Z, Arslan O.
    Transfus Apher Sci; 2013 Apr; 48(2):257-61. PubMed ID: 23433825
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  • 42. Prospective RBC phenotype matching in a stroke-prevention trial in sickle cell anemia: a multicenter transfusion trial.
    Vichinsky EP, Luban NL, Wright E, Olivieri N, Driscoll C, Pegelow CH, Adams RJ, Stroke Prevention Trail in Sickle Cell Anemia.
    Transfusion; 2001 Sep; 41(9):1086-92. PubMed ID: 11552063
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  • 43. RHCE variant alleles and risk of alloimmunization in Brazilians.
    Arnoni CP, Vendrame TAP, Silva FS, Cortez AJP, Latini FRM, Castilho L.
    Immunohematology; 2022 Dec 01; 38(4):123-129. PubMed ID: 36789463
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  • 44. Optimized Antigen-Matched in Sickle Cell Disease Patients: Chances and Challenges in Molecular Times - the Brazilian Way.
    Castilho L, Dinardo CL.
    Transfus Med Hemother; 2018 Jul 01; 45(4):258-262. PubMed ID: 30283275
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  • 45. 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 01; 58(6):1363-1371. PubMed ID: 29664198
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  • 46. [Gene Polymorphism 24 Rare Blood Group Antigens of 11 RBC Blood Group Systems in Manchu Population of Harbin Area in China].
    Liu Y, Bi DM, Zhao SZ, Yan TY, Lu FL, Wang X, Jiang PY.
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2017 Dec 01; 25(6):1799-1803. PubMed ID: 29262919
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  • 50. Identification of RHCE and KEL alleles in large cohorts of Afro-Caribbean and Comorian donors by multiplex SNaPshot and fragment assays: a transfusion support for sickle cell disease patients.
    Silvy M, Di Cristofaro J, Beley S, Papa K, Rits M, Richard P, Chiaroni J, Bailly P.
    Br J Haematol; 2011 Jul 01; 154(2):260-70. PubMed ID: 21623766
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  • 52. Blood group genotype analysis for the quality improvement of reagent test red blood cells.
    Hult A, Hellberg A, Wester ES, Olausson P, Storry JR, Olsson ML.
    Vox Sang; 2005 May 01; 88(4):265-70. PubMed ID: 15877648
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  • 53. Molecular genotyping versus serological diagnosis for RH blood group typing in sickle cell patients.
    Eftekhar Z, Oodi A, Amirizadeh N, Mohammadipour M, Keikhaei Dehdezi B, Jalali Far MA.
    Expert Rev Clin Immunol; 2024 Nov 01; 20(11):1421-1426. PubMed ID: 39105247
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  • 54. Alloimmunization in patients with sickle cell disease and underrecognition of accompanying delayed hemolytic transfusion reactions.
    Coleman S, Westhoff CM, Friedman DF, Chou ST.
    Transfusion; 2019 Jul 01; 59(7):2282-2291. PubMed ID: 31021439
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  • 58. The Rh blood group system and its role in alloimmunization rate among sickle cell disease and sickle thalassemia patients in Iran.
    Jalali Far MA, Oodi A, Amirizadeh N, Mohammadipour M, Keikhaei Dehdezi B.
    Mol Genet Genomic Med; 2021 Mar 01; 9(3):e1614. PubMed ID: 33547762
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  • 60. 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 01; 111(6 Pt 1):e661-5. PubMed ID: 12777582
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