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About 23 results

ALLMedicine™ Abo Grouping Center

Research & Reviews  9 results

New ABO intron 1 variant alleles.
https://doi.org/10.21307/immunohematology-2021-029
Immunohematology Fennell K, Keller MA et. al.

Dec 30th, 2021 - Unusual and discrepant ABO phenotypes are often due to genetic variants that lead to altered levels or activity of ABO transferases and consequently to altered expression of ABO antigens. This report describes eight genetic alterations found in 15...

Analysis of ABO grouping discrepancies among patients from a tertiary hospital in Korea.
https://doi.org/10.1016/j.transci.2021.103230
Transfusion and Apheresis Science : Official Journal of T... Heo WY, Chung YN et. al.

Aug 18th, 2021 - Accurate ABO typing is essential for preventing ABO incompatibility reactions. However, the causes of ABO grouping discrepancy has not been sufficiently studied, and it may vary among different ethnic populations. Thus, the aim of this retrospecti...

A Flow Cytometric Study of Reagent Cells to Resolve ABO Typing Discrepancy.
https://doi.org/10.1093/ajcp/aqaa117
American Journal of Clinical Pathology; Maracaja DLV, Qiao J et. al.

Oct 14th, 2020 - RBC alloantibodies can lead to ABO grouping discrepancies unrelated to A or B antigens or antibodies posing challenges in the blood bank testing. Routine blood bank testing and flow cytometry were used to immunophenotype reagent cells and elucidat...

Prevalence of and mothers' knowledge, attitude and practice towards glucose-6-phosphate...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7045182
BMJ Open; Kasemy ZA, Bahbah WA et. al.

Feb 28th, 2020 - Neonatal jaundice (NNJ) is a frequent complication of glucose-6-phosphate dehydrogenase (G6PD) deficiency. To estimate the prevalence of G6PD deficiency among neonates with jaundice and to assess mothers' perception towards G6PD and NNJ. A cross-s...

Cis-AB, the Blood Group of Many Faces, Is a Conundrum to the Novice Eye.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6240514
Annals of Laboratory Medicine; Chun S, Choi S et. al.

Nov 16th, 2018 - Cis-AB, a rare ABO variant, is caused by a gene mutation that results in a single glycosyltransferase enzyme with dual A and B glycosyltransferase activities. It is the most frequent ABO subgroup in Korea, and it occurs more frequently in the East...

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