These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

131 related articles for article (PubMed ID: 29469208)

  • 1. Molecular characterization and multidisciplinary management of Gerbich hemolytic disease of the newborn.
    Levitt RN; Gourri E; Gassner C; Banez-Sese G; Salam A; Denomme GA; Yang E
    Pediatr Blood Cancer; 2018 Jun; 65(6):e27014. PubMed ID: 29469208
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetic background of the rare Yus and Gerbich blood group phenotypes: homologous regions of the GYPC gene contribute to deletion alleles.
    Gourri E; Denomme GA; Merki Y; Scharberg EA; Vrignaud C; Frey BM; Peyrard T; Gassner C
    Br J Haematol; 2017 May; 177(4):630-640. PubMed ID: 28272739
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The Gerbich blood group system: old knowledge, new importance.
    Jaskiewicz E; Peyrard T; Kaczmarek R; Zerka A; Jodlowska M; Czerwinski M
    Transfus Med Rev; 2018 Apr; 32(2):111-116. PubMed ID: 29540278
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The Gerbich blood group system: a review.
    Walker PS; Reid ME
    Immunohematology; 2010; 26(2):60-5. PubMed ID: 20932076
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Co-presence of a point mutation and a deletion of exon 3 in the glycophorin C gene and concomitant production of a Gerbich-related antibody.
    King MJ; Kosanke J; Reid ME; Poole J; Banks J; Hemming NJ; Smythe J; Martin PG
    Transfusion; 1997 Oct; 37(10):1027-34. PubMed ID: 9354820
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hemolytic disease of the fetus and newborn due to anti-Ge3: combined antibody-dependent hemolysis and erythroid precursor cell growth inhibition.
    Blackall DP; Pesek GD; Montgomery MM; Oza KK; Arndt PA; Garratty G; Shahcheraghi A; Denomme GA
    Am J Perinatol; 2008 Oct; 25(9):541-5. PubMed ID: 18720327
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Anti-Ge3 causes late-onset hemolytic disease of the newborn: the fourth case in three Hispanic families.
    Pate LL; Myers JC; Palma JP; Viele M; Galel SA; Ferrer Z; Gonzalez CL; Benitz WE; Garratty G; Fontaine MJ
    Transfusion; 2013 Oct; 53(10):2152-7. PubMed ID: 23241141
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic diversity of Gerbich alleles in Brazilians reveals an unexpected prevalence of the GE:-2,-3,4 phenotype.
    Arnoni CP; Silva NM; Silva FS; Parreira RM; Vendrame T; Miola MP; Muniz J; Cortez A; Valvasori M; de Araujo EP; Dalmazzo L; Freitas A; Latini F; Castilho L
    Vox Sang; 2023 Oct; 118(10):873-880. PubMed ID: 37551744
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Retrospective Analysis of Irregular Antibodies Causing Hemolytic Disease of the Fetus and Newborn in Jiangxi Province].
    Liu X; LE F; Wang LH; Shu J; Xu XY
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2023 Feb; 31(1):215-220. PubMed ID: 36765502
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Late onset neonatal anaemia due to maternal anti-Ge: possible association with destruction of eythroid progenitors.
    Arndt PA; Garratty G; Daniels G; Green CA; Wilkes AM; Hunt P; Do J; Glenn S; Peterson D
    Transfus Med; 2005 Apr; 15(2):125-32. PubMed ID: 15859979
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Analysis of Screening Results in 501 Newborns with Hemolytic Disease].
    Ma X; Chen FZ; Hong Q
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2019 Feb; 27(1):192-196. PubMed ID: 30738469
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Compound heterozygosity induces a rare Gerbich-negative phenotype in an immunized blood donor.
    Petermann S; Mayer V; Carbol A; Opitz A; Flesch BK
    Transfusion; 2024 Feb; 64(2):406-411. PubMed ID: 38235836
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A mild acute hemolytic transfusion reaction in a patient with alloanti-Ge3: a case report and review of the literature.
    Baughn MR; Whitacre P; Lo GS; Pandey S; Lane TA
    Transfusion; 2011 Sep; 51(9):1966-71. PubMed ID: 21392022
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Occurrence of Rare Deletional Yus and Gerbich Alleles in Syria and Neighbouring Countries.
    Gassner C; Scherer V; Zanolin-Purin D; Scharberg EA; Flesch B
    Transfus Med Hemother; 2022 Dec; 49(6):358-367. PubMed ID: 36654979
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Positive Coomb's test in newborns; causes and clinical consequences Summary of cases diagnosed in the Blood Bank in the years 2005 to 2012].
    Kristinsdottir T; Kjartansson S; Hardardottir H; Jonsson T; Halldorsdottir AM
    Laeknabladid; 2016 Jul; 102(7-8):326-31. PubMed ID: 27531851
    [TBL] [Abstract][Full Text] [Related]  

  • 16. High frequency antigens of human erythrocyte membrane sialoglycoproteins, V. Characterization of the Gerbich blood group antigens: Ge2 and Ge3.
    Dahr W; Kiedrowski S; Blanchard D; Hermand P; Moulds JJ; Cartron JP
    Biol Chem Hoppe Seyler; 1987 Oct; 368(10):1375-83. PubMed ID: 3426806
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Three non-classical mechanisms for anemic disease of the fetus and newborn, based on maternal anti-Kell, anti-Ge3, anti-M, and anti-Jr
    Ohto H; Denomme GA; Ito S; Ishida A; Nollet KE; Yasuda H
    Transfus Apher Sci; 2020 Oct; 59(5):102949. PubMed ID: 32994126
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Fatal hemolytic disease of the newborn due to anti-B Isohemagglutinin: An unfamiliar presentation of a familiar disease.
    Longacre M; Bendapudi PK
    Transfusion; 2024 Jan; 64(1):185-188. PubMed ID: 38069508
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular basis of glycophorin C variants and their associated blood group antigens.
    Reid ME; Spring FA
    Transfus Med; 1994 Jun; 4(2):139-46. PubMed ID: 7921050
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The risk assessment study for hemolytic disease of the fetus and newborn in a University Hospital in Turkey.
    Altuntas N; Yenicesu I; Himmetoglu O; Kulali F; Kazanci E; Unal S; Aktas S; Hirfanoglu I; Onal E; Turkyilmaz C; Ergenekon E; Koc E; Atalay Y
    Transfus Apher Sci; 2013 Jun; 48(3):377-80. PubMed ID: 23619329
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.