Detalles de la búsqueda
1.
A cold case of hemolytic disease of the fetus and newborn resolved by genomic sequencing and population studies to define a new antigen in the Rh system.
Transfusion
; 64(6): 1171-1176, 2024 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-38686705
2.
Recurrent pregnancy loss in a patient with anti-Rh17.
Transfus Med
; 34(1): 66-70, 2024 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-37941301
3.
A case of haemolytic disease of the fetus and newborn attributed to a novel antigen in the RHAG blood group system.
Vox Sang
; 118(12): 1095-1099, 2023 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-38095046
4.
Hemolytic disease of the fetus and newborn caused by anti-sD antibody in a GP.Mur/Mur Thai mother and review of the prevalence of sD in Thai blood donors.
Transfusion
; 62(10): 2137-2142, 2022 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-36062546
5.
Fatal haemolytic transfusion reaction due to anti-Ena and identification of a novel GYPA c.295delG variant in a Thai family.
Vox Sang
; 117(11): 1327-1331, 2022 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-36102166
6.
A new high-prevalence LW antigen detected by an antibody in an Indigenous Australian homozygous for LW*A c.309C>A variant.
Vox Sang
; 117(7): 958-965, 2022 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-35412682
7.
Glycoproteomic and Phenotypic Elucidation of B4GALNT2 Expression Variants in the SID Histo-Blood Group System.
Int J Mol Sci
; 23(7)2022 Apr 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-35409292
8.
Targeted exome sequencing designed for blood group, platelet, and neutrophil antigen investigations: Proof-of-principle study for a customized single-test system.
Transfusion
; 60(9): 2108-2120, 2020 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-32687227
9.
Frequency of Mia (MNS7) and Classification of Mia-Positive Hybrid Glycophorins in an Australian Blood Donor Population.
Transfus Med Hemother
; 47(4): 279-286, 2020 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-32884500
10.
A DEL phenotype attributed to RHD Exon 9 sequence deletion: slipped-strand mispairing and blood group polymorphisms.
Transfusion
; 58(3): 685-691, 2018 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-29214630
11.
Targeted exome sequencing defines novel and rare variants in complex blood group serology cases for a red blood cell reference laboratory setting.
Transfusion
; 58(2): 284-293, 2018 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-29119571
12.
Anti-D in a mother, hemizygous for the variant RHD*DNB gene, associated with hemolytic disease of the fetus and newborn.
Transfusion
; 57(8): 1938-1943, 2017 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-28639307
13.
Evaluation of targeted exome sequencing for 28 protein-based blood group systems, including the homologous gene systems, for blood group genotyping.
Transfusion
; 57(4): 1078-1088, 2017 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-28338218
14.
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.
Transfusion
; 56(9): 2322-30, 2016 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-27390888
15.
A Houdini act: Transient loss of Jka resulting in anti-Jk3 antibody formation.
Transfus Med
; 31(4): 303-304, 2021 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-33709488
16.
The RHD(1227G>A) DEL-associated allele is the most prevalent DEL allele in Australian D- blood donors with C+ and/or E+ phenotypes.
Transfusion
; 54(11): 2931-40, 2014 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-24894016
17.
Modified expression of the KEL2 (k) blood group antigen attributed to p.Leu196Val amino acid change three residues from the K/k antigen polymorphism site: implications for donor screening.
Transfusion
; 59(3): 1156-1158, 2019 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-30586164
18.
A proposed new low-frequency antigen in the Augustine blood group system associated with a severe case of hemolytic disease of the fetus and newborn.
Transfusion
; 58(5): 1320-1322, 2018 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-29504136
19.
Anti-D in pregnant women with the RHD(IVS3+1G>A)-associated DEL phenotype.
Transfusion
; 52(9): 2016-9, 2012 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-22313164
20.
An alloantibody in a homozygous GYP*Mur individual defines JENU (MNS49), a new high-frequency antigen on glycophorin B.
Transfusion
; 57(3): 716-717, 2017 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-27917500