BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

408 related articles for article (PubMed ID: 19295544)

  • 1. The complete evaluation of erythrocytosis: congenital and acquired.
    Patnaik MM; Tefferi A
    Leukemia; 2009 May; 23(5):834-44. PubMed ID: 19295544
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Evaluation of "increased" hemoglobin in the JAK2 mutations era: a diagnostic algorithm based on genetic tests.
    Tefferi A; Pardanani A
    Mayo Clin Proc; 2007 May; 82(5):599-604. PubMed ID: 17493421
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Molecular study of congenital erythrocytosis in 70 unrelated patients revealed a potential causal mutation in less than half of the cases (Where is/are the missing gene(s)?).
    Bento C; Almeida H; Maia TM; Relvas L; Oliveira AC; Rossi C; Girodon F; Fernandez-Lago C; Aguado-Diaz A; Fraga C; Costa RM; Araújo AL; Silva J; Vitória H; Miguel N; Silveira MP; Martin-Nuñez G; Ribeiro ML
    Eur J Haematol; 2013 Oct; 91(4):361-8. PubMed ID: 23859443
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Elevated serum erythropoietin levels in patients with Budd-Chiari syndrome secondary to polycythemia vera: clinical implications for the role of JAK2 mutation analysis.
    Thurmes PJ; Steensma DP
    Eur J Haematol; 2006 Jul; 77(1):57-60. PubMed ID: 16827884
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Diagnostic value of serum erythropoietin level in patients with absolute erythrocytosis.
    Mossuz P; Girodon F; Donnard M; Latger-Cannard V; Dobo I; Boiret N; Lecron JC; Binquet C; Barro C; Hermouet S; Praloran V
    Haematologica; 2004 Oct; 89(10):1194-8. PubMed ID: 15477203
    [TBL] [Abstract][Full Text] [Related]  

  • 6. JAK2 unmutated erythrocytosis: 2023 Update on diagnosis and management.
    Gangat N; Szuber N; Tefferi A
    Am J Hematol; 2023 Jun; 98(6):965-981. PubMed ID: 36966432
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Blood p50 evaluation enhances diagnostic definition of isolated erythrocytosis.
    Rumi E; Passamonti F; Pagano L; Ammirabile M; Arcaini L; Elena C; Flagiello A; Tedesco R; Vercellati C; Marcello AP; Pietra D; Moratti R; Cazzola M; Lazzarino M
    J Intern Med; 2009 Feb; 265(2):266-74. PubMed ID: 18793248
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Polycythemia vera.
    Landolfi R; Nicolazzi MA; Porfidia A; Di Gennaro L
    Intern Emerg Med; 2010 Oct; 5(5):375-84. PubMed ID: 20237866
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Diagnostic Performance of Erythropoietin Levels in Polycythemia Vera: Experience at a Comprehensive Cancer Center.
    Davila-Gonzalez D; Barrios-Ruiz A; Fountain E; Cheng L; Masarova L; Verstovsek S; Rojas-Hernandez CM
    Clin Lymphoma Myeloma Leuk; 2021 Apr; 21(4):224-229. PubMed ID: 33349602
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Polycythemia and oxygen sensing.
    Maran J; Prchal J
    Pathol Biol (Paris); 2004 Jun; 52(5):280-4. PubMed ID: 15217714
    [TBL] [Abstract][Full Text] [Related]  

  • 11. JAK2 unmutated erythrocytosis: current diagnostic approach and therapeutic views.
    Gangat N; Szuber N; Pardanani A; Tefferi A
    Leukemia; 2021 Aug; 35(8):2166-2181. PubMed ID: 34021251
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Polycythemia vera: scientific advances and current practice.
    Tefferi A; Spivak JL
    Semin Hematol; 2005 Oct; 42(4):206-20. PubMed ID: 16210034
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Usefulness of JAK2V617F mutation in distinguishing idiopathic erythrocytosis from polycythemia vera.
    Rossi D; Cortini F; Deambrogi C; Barbieri C; Cerri M; Franceschetti S; Conconi A; Capello D; Gaidano G
    Leuk Res; 2007 Jan; 31(1):97-101. PubMed ID: 16620973
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The frequency of JAK2 exon 12 mutations in idiopathic erythrocytosis patients with low serum erythropoietin levels.
    Percy MJ; Scott LM; Erber WN; Harrison CN; Reilly JT; Jones FG; Green AR; McMullin MF
    Haematologica; 2007 Dec; 92(12):1607-14. PubMed ID: 18055983
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Hereditary erythrocytosis, thrombocytosis and neutrophilia.
    Hong WJ; Gotlib J
    Best Pract Res Clin Haematol; 2014 Jun; 27(2):95-106. PubMed ID: 25189721
    [TBL] [Abstract][Full Text] [Related]  

  • 16. "Benign erythrocytosis" and other familial and congenital polycythemias.
    Prchal JT; Sokol L
    Eur J Haematol; 1996 Oct; 57(4):263-8. PubMed ID: 8982288
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Novel Homozygous Mutation of the Internal Translation Initiation Start Site of VHL is Exclusively Associated with Erythrocytosis: Indications for Distinct Functional Roles of von Hippel-Lindau Tumor Suppressor Isoforms.
    Bartels M; van der Zalm MM; van Oirschot BA; Lee FS; Giles RH; Kruip MJ; Gitz-Francois JJ; Van Solinge WW; Bierings M; van Wijk R
    Hum Mutat; 2015 Nov; 36(11):1039-42. PubMed ID: 26224408
    [TBL] [Abstract][Full Text] [Related]  

  • 18. How to manage polycythemia vera.
    Passamonti F
    Leukemia; 2012 May; 26(5):870-4. PubMed ID: 22157736
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinical features of acquired erythrocytosis: Low levels of serum erythropoietin in a subset of non-neoplastic erythrocytosis patients.
    Mori Y; Araki M; Morishita S; Imai M; Edahiro Y; Ito M; Ochiai T; Shirane S; Hashimoto Y; Yasuda H; Ando J; Ando M; Komatsu N
    Cancer Med; 2023 Jan; 12(2):1079-1089. PubMed ID: 35775283
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Current diagnostic criteria for the chronic myeloproliferative disorders (MPD) essential thrombocythemia (ET), polycythemia vera (PV) and chronic idiopathic myelofibrosis (CIMF).
    Michiels JJ; Bernema Z; Van Bockstaele D; De Raeve H; Schroyens W
    Pathol Biol (Paris); 2007 Mar; 55(2):92-104. PubMed ID: 16919893
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 21.