BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

258 related articles for article (PubMed ID: 33074480)

  • 1. Characterization of hereditary red blood cell membranopathies using combined targeted next-generation sequencing and osmotic gradient ektacytometry.
    Vives-Corrons JL; Krishnevskaya E; Rodriguez IH; Ancochea A
    Int J Hematol; 2021 Feb; 113(2):163-174. PubMed ID: 33074480
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Red cell ektacytometry in two patients with chronic hemolytic anemia and three new α-spectrin variants.
    Vives-Corrons JL; Krishnevskaya E; Hernández-Rodriguez I; Payán-Pernia S; Sevilla ÁFR; Badell I
    Ann Hematol; 2022 Mar; 101(3):549-555. PubMed ID: 34845540
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Use of Laser Assisted Optical Rotational Cell Analyzer (LoRRca MaxSis) in the Diagnosis of RBC Membrane Disorders, Enzyme Defects, and Congenital Dyserythropoietic Anemias: A Monocentric Study on 202 Patients.
    Zaninoni A; Fermo E; Vercellati C; Consonni D; Marcello AP; Zanella A; Cortelezzi A; Barcellini W; Bianchi P
    Front Physiol; 2018; 9():451. PubMed ID: 29755372
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Osmotic gradient ektacytometry: A valuable screening test for hereditary spherocytosis and other red blood cell membrane disorders.
    Llaudet-Planas E; Vives-Corrons JL; Rizzuto V; Gómez-Ramírez P; Sevilla Navarro J; Coll Sibina MT; García-Bernal M; Ruiz Llobet A; Badell I; Velasco-Puyó P; Dapena JL; Mañú-Pereira MM
    Int J Lab Hematol; 2018 Feb; 40(1):94-102. PubMed ID: 29024480
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Diagnostic tool for red blood cell membrane disorders: Assessment of a new generation ektacytometer.
    Da Costa L; Suner L; Galimand J; Bonnel A; Pascreau T; Couque N; Fenneteau O; Mohandas N; ;
    Blood Cells Mol Dis; 2016 Jan; 56(1):9-22. PubMed ID: 26603718
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Clinical utility of targeted next-generation sequencing panel in routine diagnosis of hereditary hemolytic anemia: A national reference laboratory experience.
    Agarwal AM; McMurty V; Clayton AL; Bolia A; Reading NS; Mani C; Patel JL; Rets A
    Eur J Haematol; 2023 Jun; 110(6):688-695. PubMed ID: 36825813
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Asymptomatic elevation of the hyperchromic red blood cell subpopulation is associated with decreased red cell deformability.
    Deuel JW; Lutz HU; Misselwitz B; Goede JS
    Ann Hematol; 2012 Sep; 91(9):1427-34. PubMed ID: 22526368
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Next-generation osmotic gradient ektacytometry for the diagnosis of hereditary spherocytosis: interlaboratory method validation and experience.
    Lazarova E; Gulbis B; Oirschot BV; van Wijk R
    Clin Chem Lab Med; 2017 Mar; 55(3):394-402. PubMed ID: 27559691
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Hereditary spherocytosis.
    Iolascon A; Avvisati RA; Piscopo C
    Transfus Clin Biol; 2010 Sep; 17(3):138-42. PubMed ID: 20655264
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Advances in understanding the pathogenesis of red cell membrane disorders.
    Iolascon A; Andolfo I; Russo R
    Br J Haematol; 2019 Oct; 187(1):13-24. PubMed ID: 31364155
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A Systematic review on diagnostic methods of red cell membrane disorders in Asia.
    Silva R; Amarasinghe D; Perera S; Premawardhena A
    Int J Lab Hematol; 2022 Apr; 44(2):248-262. PubMed ID: 35068068
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular diagnosis of hereditary spherocytosis by multi-gene target sequencing in Korea: matching with osmotic fragility test and presence of spherocyte.
    Choi HS; Choi Q; Kim JA; Im KO; Park SN; Park Y; Shin HY; Kang HJ; Kook H; Kim SY; Kim SJ; Kim I; Kim JY; Kim H; Park KD; Park KB; Park M; Park SK; Park ES; Park JA; Park JE; Park JK; Baek HJ; Seo JH; Shim YJ; Ahn HS; Yoo KH; Yoon HS; Won YW; Lee KS; Lee KC; Lee MJ; Lee SA; Lee JA; Lee JM; Lee JH; Lee JW; Lim YT; Jung HJ; Chueh HW; Choi EJ; Jung HL; Kim JH; Lee DS;
    Orphanet J Rare Dis; 2019 May; 14(1):114. PubMed ID: 31122244
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Recent advances in the understanding of the erythrocyte membrane.
    Lam SK; Quah TC
    J Singapore Paediatr Soc; 1991; 33(3-4):140-8. PubMed ID: 1812330
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Hereditary red cell membrane disorders and laboratory diagnostic testing.
    King MJ; Zanella A
    Int J Lab Hematol; 2013 Jun; 35(3):237-43. PubMed ID: 23480868
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Application of systematic etiological analysis in final and differential diagnosis of hereditary hemolytic anemia].
    Li JY; Gu HH; Zheng SJ; Zha ZS; Hua MX; Jiang JJ; Cai B; Zhou L; Jia Y; Fang CP; Qian BH
    Zhonghua Xue Ye Xue Za Zhi; 2016 Jun; 37(6):512-6. PubMed ID: 27431078
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Red cell membrane disorders.
    Narla J; Mohandas N
    Int J Lab Hematol; 2017 May; 39 Suppl 1():47-52. PubMed ID: 28447420
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Identification of red blood cell membrane defects in a patient with hereditary spherocytosis using next‑generation sequencing technology and matrix‑assisted laser desorption/ionization time‑of‑flight mass spectrometry.
    Şener LT; Aktan M; Albeniz G; Şener A; Üstek D; Albeniz I
    Mol Med Rep; 2019 May; 19(5):3912-3922. PubMed ID: 30896804
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Diagnosis and clinical management of red cell membrane disorders.
    Kalfa TA
    Hematology Am Soc Hematol Educ Program; 2021 Dec; 2021(1):331-340. PubMed ID: 34889366
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A Novel
    Jang W; Kim SK; Nahm CH; Choi JW; Kim JJ; Moon Y
    Ann Clin Lab Sci; 2021 Jan; 51(1):136-139. PubMed ID: 33653793
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.