Variants of RhD--current testing and clinical consequences.
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Rh Immunoprophylaxis for Women With a Serologic Weak D PhenotypePrenatal testing for hemolytic disease of the newborn and fetal neonatal alloimmune thrombocytopenia - current status.Pre-analytical conditions in non-invasive prenatal testing of cell-free fetal RHDRecommendations for the prevention and treatment of haemolytic disease of the foetus and newborn.It's time to phase in RHD genotyping for patients with a serologic weak D phenotype. College of American Pathologists Transfusion Medicine Resource Committee Work Group.Occurrence of anti-D alloantibodies among pregnant women in Kasese District, Western Uganda.Rh D blood group conversion using transcription activator-like effector nucleases.'Chameleonic' Serological Findings Leading to Life-Threatening Hemolytic Transfusion Reactions.Integration of noninvasive prenatal prediction of fetal blood group into clinical prenatal care.Red cell transfusion and the immune system.Considerations of red blood cell molecular testing in transfusion medicine.Screening for DEL phenotype in RhD negative Indians.Diverse and novel RHD variants in Australian blood donors with a weak D phenotype: implication for transfusion management.Pathology Consultation on Patients With a Large Rh Immune Globulin Dose Requirement.Serological weak D phenotypes: a review and guidance for interpreting the RhD blood type using the RHD genotype.A D+ blood donor with a novel RHD*D-CE(5-6)-D gene variant exhibits the low-frequency antigen RH23 (D(W) ) characteristic of the partial DVa phenotype.Extensive functional analyses of RHD splice site variants: Insights into the potential role of splicing in the physiology of Rh.Non-invasive foetal RhD genotyping in admixed populations.Prevalence of RhD variants among blood donors at Gulu Regional Blood Bank, Gulu, Northern Uganda.Antibodies to biotinylated red blood cells in adults and infants: improved detection, partial characterization, and dependence on red blood cell-biotin dose.Application of Multiplex Ligation-Dependent Probe Amplification Assay for Genotyping Major Blood Group Systems Including DEL Variants in the D-Negative Korean Population.Targeted exome sequencing defines novel and rare variants in complex blood group serology cases for a red blood cell reference laboratory setting.RHD genotype and zygosity analysis in the Chinese Southern Han D+, D- and D variant donors using the multiplex ligation-dependent probe amplification assay.An effective diagnostic strategy for accurate detection of RhD variants including Asian DEL type in apparently RhD-negative blood donors in Korea.A DEL phenotype attributed to RHD Exon 9 sequence deletion: slipped-strand mispairing and blood group polymorphisms.Antigen Density Dictates Immune Responsiveness following Red Blood Cell Transfusion.Anti-D in a mother, hemizygous for the variant RHD*DNB gene, associated with hemolytic disease of the fetus and newborn.RHD alleles among pregnant women with serologic discrepant weak D phenotypes from a multiethnic population and risk of alloimmunization.RHD-specific microRNA for regulation of the DEL blood group: integration of computational and experimental approaches.Strategies to identify candidates for D variant genotyping.Fetal RHD Genotyping from Circulating Cell-Free Fetal DNA in Plasma of Rh Negative Pregnant Women in Iran.The RHD(1227G>A) DEL-associated allele is the most prevalent DEL allele in Australian D- blood donors with C+ and/or E+ phenotypes.Prenatal non-invasive foetal RHD genotyping: diagnostic accuracy of a test as a guide for appropriate administration of antenatal anti-D immunoprophylaxis.Frequency and characterization of known and novel RHD variant alleles in 37 782 Dutch D-negative pregnant women.Rhesus blood group haplotype frequencies among blood donors in southwestern Uganda.Transfusion Support of Minority Patients: Extended Antigen Donor Typing and Recruitment of Minority Blood DonorsWeak D Testing is not Required for D- Patients With C-E- Phenotype
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P2860
Variants of RhD--current testing and clinical consequences.
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
@sq
artículo científico
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name
Variants of RhD--current testing and clinical consequences.
@en
type
label
Variants of RhD--current testing and clinical consequences.
@en
prefLabel
Variants of RhD--current testing and clinical consequences.
@en
P2860
P356
P1476
Variants of RhD--current testing and clinical consequences.
@en
P2093
Geoff Daniels
P2860
P304
P356
10.1111/BJH.12275
P407
P577
2013-02-25T00:00:00Z