BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

168 related articles for article (PubMed ID: 18932080)

  • 1. Hereditary spherocytosis with high fetal hemoglobin: an interesting case.
    Kar R; Saxena R; Pati HP
    Hemoglobin; 2008; 32(5):520-3. PubMed ID: 18932080
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Comparison study of the eosin-5'-maleimide binding test, flow cytometric osmotic fragility test, and cryohemolysis test in the diagnosis of hereditary spherocytosis.
    Park SH; Park CJ; Lee BR; Cho YU; Jang S; Kim N; Koh KN; Im HJ; Seo JJ; Park ES; Lee JW; Yoo KH; Jung HL
    Am J Clin Pathol; 2014 Oct; 142(4):474-84. PubMed ID: 25239414
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A Case of Hereditary Spherocytosis Caused by a Novel Homozygous Mutation in the
    Yang K; Ren Q; Wu Y; Zhou Y; Yin X
    Hemoglobin; 2019 Mar; 43(2):140-144. PubMed ID: 31190573
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Evaluation of eosin-5-maleimide flow cytometric test in diagnosis of hereditary spherocytosis.
    Kar R; Mishra P; Pati HP
    Int J Lab Hematol; 2010 Feb; 32(1 Pt 2):8-16. PubMed ID: 18782334
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Using the eosin-5-maleimide binding test in the differential diagnosis of hereditary spherocytosis and hereditary pyropoikilocytosis.
    King MJ; Telfer P; MacKinnon H; Langabeer L; McMahon C; Darbyshire P; Dhermy D
    Cytometry B Clin Cytom; 2008 Jul; 74(4):244-50. PubMed ID: 18454487
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Rapid flow cytometric test using eosin-5-maleimide for diagnosis of red blood cell membrane disorders.
    Tachavanich K; Tanphaichitr VS; Utto W; Viprakasit V
    Southeast Asian J Trop Med Public Health; 2009 May; 40(3):570-5. PubMed ID: 19842445
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The affinity glycated hemoglobin in a family with hereditary spherocytosis and in other non-hemoglobinopathic hemolytic anemias.
    Krauss JS; Hahn DA; Harper D; Shell S; Baisden CR
    Ann Clin Lab Sci; 1987; 17(5):331-8. PubMed ID: 2445253
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Essects of splenectomy on the proliferation of HbF-containing erythrocytes in hereditary spherocytosis].
    Ishizu K; Kakishita E; Nagai K
    Rinsho Ketsueki; 1972 Jun; 13(3):378-86. PubMed ID: 4566888
    [No Abstract]   [Full Text] [Related]  

  • 9. Flow cytometry as a diagnostic tool for hereditary spherocytosis.
    Stoya G; Gruhn B; Vogelsang H; Baumann E; Linss W
    Acta Haematol; 2006; 116(3):186-91. PubMed ID: 17016037
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Hemoglobin Kenya composed of alpha- and ((A)gammabeta)-fusion-globin chains, associated with hereditary persistence of fetal hemoglobin.
    Wilcox I; Boettger K; Greene L; Malek A; Davis L; Steinberg MH; Luo HY; Chui DH
    Am J Hematol; 2009 Jan; 84(1):55-8. PubMed ID: 19006227
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Hereditary spherocytosis diagnosed with the eosin-5'-maleimide binding test.
    Watanabe T; Ono H; Tajima I; Ishigaki H; Hakamata A; Shirai M; Endoh A; Hongo T
    Pediatr Int; 2014 Jun; 56(3):427-9. PubMed ID: 24894931
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Presence of cytosolic peroxiredoxin 2 in the erythrocyte membrane of patients with hereditary spherocytosis.
    Rocha S; Vitorino RM; Lemos-Amado FM; Castro EB; Rocha-Pereira P; Barbot J; Cleto E; Ferreira F; Quintanilha A; Belo L; Santos-Silva A
    Blood Cells Mol Dis; 2008; 41(1):5-9. PubMed ID: 18387321
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clinical and hematologic features of 300 patients affected by hereditary spherocytosis grouped according to the type of the membrane protein defect.
    Mariani M; Barcellini W; Vercellati C; Marcello AP; Fermo E; Pedotti P; Boschetti C; Zanella A
    Haematologica; 2008 Sep; 93(9):1310-7. PubMed ID: 18641031
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Coinheritance of sickle cell anemia and hereditary spherocytosis.
    Selcuk Duru N; Celkan T; Civilibal M; Ozbek NO; Basak AN; Elevli M
    Pediatr Blood Cancer; 2008 Oct; 51(4):560-3. PubMed ID: 18561176
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [A case of association of Hb C Ziguinchor (alpha A2 beta 6-2 (A3) Glu replaced by Val beta 58 (E2) Pro replaced by Arg) with a hereditary persistence of fetal hemoglobin (HPFH). Clinical and biological results].
    Fabritius H; Ferney-Saris L; Sanogo I; Sangare A; Cabannes R
    Med Trop (Mars); 1987; 47(2):177-9. PubMed ID: 2442578
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Rapid flow cytometric test for the diagnosis of membrane cytoskeleton-associated haemolytic anaemia.
    King MJ; Behrens J; Rogers C; Flynn C; Greenwood D; Chambers K
    Br J Haematol; 2000 Dec; 111(3):924-33. PubMed ID: 11122157
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Differential diagnosis of hereditary hemolytic disorders.
    Jaffe ER
    Med Times; 1972 Mar; 100(3):254-72. PubMed ID: 4559277
    [No Abstract]   [Full Text] [Related]  

  • 18. Screening and confirmation of hereditary spherocytosis in children using a CELL-DYN Sapphire haematology analyser.
    Rooney S; Hoffmann JJ; Cormack OM; McMahon C
    Int J Lab Hematol; 2015 Feb; 37(1):98-104. PubMed ID: 24739214
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Steroid therapy may be effective in augmenting hemoglobin levels during hemolytic crises in children with hereditary spherocytosis.
    Ballin A; Waisbourd-Zinman O; Saab H; Yacobovich J; Zoldan M; Barzilai-Birenbaum S; Yaniv I; Tamary H
    Pediatr Blood Cancer; 2011 Aug; 57(2):303-5. PubMed ID: 21480468
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Physiologically important secondary modifications of red cell membrane in hereditary spherocytosis-evidence for in vivo oxidation and lipid rafts protein variations.
    Margetis P; Antonelou M; Karababa F; Loutradi A; Margaritis L; Papassideri I
    Blood Cells Mol Dis; 2007; 38(3):210-20. PubMed ID: 17208471
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.