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Journal Abstract Search


253 related items for PubMed ID: 30026182

  • 21. Systematic RH genotyping and variant identification in French donors of African origin.
    Kappler-Gratias S, Auxerre C, Dubeaux I, Beolet M, Ripaux M, Le Pennec PY, Pham BN.
    Blood Transfus; 2014 Jan; 12 Suppl 1(Suppl 1):s264-72. PubMed ID: 23867180
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  • 22. Impact of Red Blood Cell Antigen Matching on Alloimmunization and Transfusion Complications in Patients with Sickle Cell Disease: A Systematic Review.
    Fasano RM, Meyer EK, Branscomb J, White MS, Gibson RW, Eckman JR.
    Transfus Med Rev; 2019 Jan; 33(1):12-23. PubMed ID: 30122266
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  • 24. Barriers to using molecularly typed minority red blood cell donors in support of chronically transfused adult patients with sickle cell disease.
    Karafin MS, Field JJ, Gottschall JL, Denomme GA.
    Transfusion; 2015 Jun; 55(6 Pt 2):1399-406. PubMed ID: 25757390
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  • 29. Variant RH alleles and Rh immunisation in patients with sickle cell disease.
    Sippert E, Fujita CR, Machado D, Guelsin G, Gaspardi AC, Pellegrino J, Gilli S, Saad SS, Castilho L.
    Blood Transfus; 2015 Jan; 13(1):72-7. PubMed ID: 24960646
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  • 30. Predicting the effect of transfusing only phenotype-matched RBCs to patients with sickle cell disease: theoretical and practical implications.
    Castro O, Sandler SG, Houston-Yu P, Rana S.
    Transfusion; 2002 Jun; 42(6):684-90. PubMed ID: 12147019
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  • 31. Genomic characterization of the RH locus detects complex and novel structural variation in multi-ethnic cohorts.
    Wheeler MM, Lannert KW, Huston H, Fletcher SN, Harris S, Teramura G, Maki HJ, Frazar C, Underwood JG, Shaffer T, Correa A, Delaney M, Reiner AP, Wilson JG, Nickerson DA, Johnsen JM, NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium.
    Genet Med; 2019 Feb; 21(2):477-486. PubMed ID: 29955105
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  • 35. Utilising red cell antigen genotyping and serological phenotyping in sickle cell disease patients to risk-stratify patients for alloimmunisation risk.
    Shih AW, Yan MTS, Elahie AL, Barty RL, Liu Y, Berardi P, Azzam M, Siddiqui R, Parvizian MK, Mcdougall T, Heddle NM, Al-Habsi KS, Goldman M, Cote J, Athale U, Verhovsek MM.
    Transfus Med; 2020 Aug; 30(4):263-274. PubMed ID: 32432400
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  • 36. Distribution of the FYBES and RHCE*ce(733C>G) alleles in an Argentinean population: implications for transfusion medicine.
    Cotorruelo CM, Fiori SV, Borrás SE, Racca LL, Biondi CS, Racca AL.
    BMC Med Genet; 2008 May 06; 9():40. PubMed ID: 18460195
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  • 37. Relevance of RH variants in transfusion of sickle cell patients.
    Noizat-Pirenne F, Tournamille C.
    Transfus Clin Biol; 2011 Dec 06; 18(5-6):527-35. PubMed ID: 22024128
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  • 38. Accurate long-read sequencing allows assembly of the duplicated RHD and RHCE genes harboring variants relevant to blood transfusion.
    Zhang Z, An HH, Vege S, Hu T, Zhang S, Mosbruger T, Jayaraman P, Monos D, Westhoff CM, Chou ST.
    Am J Hum Genet; 2022 Jan 06; 109(1):180-191. PubMed ID: 34968422
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  • 39. [Polymorphisms of RHCE gene among serologic RhD negative donors of Han population in Chinese Jiangsu area].
    Chen Q, Xiao JY, Yu X, Huang CY, Yao GH.
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2014 Oct 06; 22(5):1428-31. PubMed ID: 25338601
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  • 40. High frequency of variant RHD genotypes among donors and patients of mixed origin with serologic weak-D phenotype.
    Dezan MR, Oliveira VB, Gomes ÇN, Luz F, Gallucci AJ, Bonifácio SL, Alencar CS, Sabino EC, Pereira AC, Krieger JE, Rocha V, Mendrone-Junior A, Dinardo CL.
    J Clin Lab Anal; 2018 Nov 06; 32(9):e22596. PubMed ID: 29943480
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