156 related articles for article (PubMed ID: 34121248)
1. D--phenotype due to RHD-RHCE hybrid transcript in a case of severe haemolytic disease of newborn with anti-Rh 17(Hrₒ) antibodies.
Mani A; Mishra G; Kulkarni S; Gupta D
Transfus Med; 2021 Oct; 31(5):383-386. PubMed ID: 34121248
[TBL] [Abstract][Full Text] [Related]
2. Maternal red blood cell alloimmunisation Working Party, literature review. RH blood group system: Rare specificities.
Floch A
Transfus Clin Biol; 2021 Aug; 28(3):314-320. PubMed ID: 33895380
[TBL] [Abstract][Full Text] [Related]
3. Recurrent pregnancy loss in a patient with anti-Rh17.
Moiz B; Salman M; Rasheed S; Qudus R; Millard G; Hyland CA; Flower RL; Wilson B; Turner R; Lopez GH; Liew YW
Transfus Med; 2024 Feb; 34(1):66-70. PubMed ID: 37941301
[TBL] [Abstract][Full Text] [Related]
4. Molecular characterization of rare D--/D-- variants in individuals of Indian origin.
Kulkarni S; Mishra G; Maru H; Parchure D; Gupta D; Bajaj AK; Sindhwani SP; Chaphekar A; Shah R; Férec C; Madkaikar M; Fichou Y
Blood Transfus; 2022 Jan; 20(1):59-65. PubMed ID: 33263520
[TBL] [Abstract][Full Text] [Related]
5. Severe hemolytic disease of the fetus and newborn due to allo-anti-D in a patient with a partial DEL phenotype arising from the variant allele described as RHD*148+1T (RHD*01EL.31).
Turley E; McGowan EC; Hyland CA; Schoeman EM; Flower RL; Skoll A; Delisle MF; Nelson T; Clarke G; Au N
Transfusion; 2018 Oct; 58(10):2260-2264. PubMed ID: 30222865
[TBL] [Abstract][Full Text] [Related]
6. 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.
Wilson B; Davison CL; Lopez GH; Millard GM; Liew YW; Powley T; Campbell T; Jadhao SS; Nagaraj SH; Perry M; Roulis EV; Toombs M; Irving DO; Flower RL; Hyland CA
Transfusion; 2024 Jun; 64(6):1171-1176. PubMed ID: 38686705
[TBL] [Abstract][Full Text] [Related]
7. Hemolytic disease of the fetus and newborn caused by anti-Hr
Sarihi R; Ahmadnejad M; Mohammadi S; Eshghi P; Herfat F; Jolharnejad S; Oodi A
Transfus Apher Sci; 2021 Feb; 60(1):102913. PubMed ID: 32943324
[TBL] [Abstract][Full Text] [Related]
8. Severe haemolytic disease of a newborn with variant D mimicking blocked-D phenomenon.
Das S; Shastry S; Baliga PB
BMJ Case Rep; 2019 Dec; 12(12):. PubMed ID: 31843772
[TBL] [Abstract][Full Text] [Related]
9. Severe anti-D haemolytic disease of fetal and newborn in rhesus D negative primigravida.
Hassan MZ; Iberahim S; Abdul Rahman WSW; Zulkafli Z; Bahar R; Ramli M; Mohd Noor NH; Mustaffa R
Malays J Pathol; 2019 Apr; 41(1):55-58. PubMed ID: 31025639
[TBL] [Abstract][Full Text] [Related]
10. The risk to future pregnancies of transfusing Rh(D)-negative females of childbearing potential with Rh(D)-positive red blood cells during trauma resuscitation is dependent on their age at transfusion.
Seheult JN; Stram MN; Pearce T; Bub CB; Emery SP; Kutner J; Watanabe-Okochi N; Sperry JL; Takanashi M; Triulzi DJ; Yazer MH
Vox Sang; 2021 Aug; 116(7):831-840. PubMed ID: 33491789
[TBL] [Abstract][Full Text] [Related]
11. Cases of RhD variants RhD*DAU2/DAU6 and RhD*weak D type 4.1 in pregnant women in Saudi Arabia.
Owaidah A; Aljuhani K; Albasri J; Alsulmi E; Alsaihati T; Alzahrani F
Acta Biomed; 2023 Mar; 94(S1):e2023080. PubMed ID: 36883669
[TBL] [Abstract][Full Text] [Related]
12. Molecular analysis of Rh transcripts and polypeptides from individuals expressing the DVI variant phenotype: an RHD gene deletion event does not generate All DVIccEe phenotypes.
Avent ND; Liu W; Jones JW; Scott ML; Voak D; Pisacka M; Watt J; Fletcher A
Blood; 1997 Mar; 89(5):1779-86. PubMed ID: 9057663
[TBL] [Abstract][Full Text] [Related]
13. Fetal blood group genotyping from DNA from maternal plasma: an important advance in the management and prevention of haemolytic disease of the fetus and newborn.
Daniels G; Finning K; Martin P; Soothill P
Vox Sang; 2004 Nov; 87(4):225-32. PubMed ID: 15585017
[TBL] [Abstract][Full Text] [Related]
14. Haemolytic disease of the fetus and newborn.
de Haas M; Thurik FF; Koelewijn JM; van der Schoot CE
Vox Sang; 2015 Aug; 109(2):99-113. PubMed ID: 25899660
[TBL] [Abstract][Full Text] [Related]
15. Non-invasive fetal RHD and RHCE genotyping from maternal plasma in alloimmunized pregnancies.
Hromadnikova I; Vesela K; Benesova B; Nekovarova K; Duskova D; Vlk R; Spalova I; Gerychova R; Hakenova A; Rosenbaumova Z; Vlasin P; Vlachova A; Palasek V; Roznakova E; Calda P
Prenat Diagn; 2005 Dec; 25(12):1079-83. PubMed ID: 16231295
[TBL] [Abstract][Full Text] [Related]
16. A case of fatal hemolytic disease of the newborn associated with-D-/-D-phenotype.
Han KS; Kim HC; Han KS; Shim WS
Am J Perinatol; 1997 Sep; 14(8):495-7. PubMed ID: 9376014
[TBL] [Abstract][Full Text] [Related]
17. Non-invasive prenatal testing for management of haemolytic disease of the fetus and newborn induced by maternal alloimmunisation.
Hyland CA; O'Brien H; Flower RL; Gardener GJ
Transfus Apher Sci; 2020 Oct; 59(5):102947. PubMed ID: 33115620
[TBL] [Abstract][Full Text] [Related]
18. Anti-C causing severe hemolytic disease of the fetus and newborn: a rare case report.
Sahoo D; Anuragaa S; Abhishekh B
Immunohematology; 2023 Apr; 39(1):11-14. PubMed ID: 37017597
[TBL] [Abstract][Full Text] [Related]
19. [Haemolytic disease of the fetus and newborn/HDFN/timing in pregnant women and prophylaxis].
Kulinska R
Akush Ginekol (Sofiia); 2014; 53(2):58-63. PubMed ID: 25098112
[TBL] [Abstract][Full Text] [Related]
20. Anti-D in a mother, hemizygous for the variant RHD*DNB gene, associated with hemolytic disease of the fetus and newborn.
Quantock KM; Lopez GH; Hyland CA; Liew YW; Flower RL; Niemann FJ; Joyce A
Transfusion; 2017 Aug; 57(8):1938-1943. PubMed ID: 28639307
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
