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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

663 related items for PubMed ID: 17074595

  • 1. Myelodysplastic syndrome associated with monosomy 7 in childhood: a retrospective study.
    Aktas D, Tuncbilek E.
    Cancer Genet Cytogenet; 2006 Nov; 171(1):72-5. PubMed ID: 17074595
    [Abstract] [Full Text] [Related]

  • 2. Monosomy 7 associated with pediatric acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS): successful management by allogeneic hematopoietic stem cell transplant (HSCT).
    Trobaugh-Lotrario AD, Kletzel M, Quinones RR, McGavran L, Proytcheva MA, Hunger SP, Malcolm J, Schissel D, Hild E, Giller RH.
    Bone Marrow Transplant; 2005 Jan; 35(2):143-9. PubMed ID: 15558042
    [Abstract] [Full Text] [Related]

  • 3. Spontaneous remission of myelodysplastic syndrome with monosomy 7 in a young boy.
    Parker TM, Klaassen RJ, Johnston DL.
    Cancer Genet Cytogenet; 2008 Apr 15; 182(2):122-5. PubMed ID: 18406874
    [Abstract] [Full Text] [Related]

  • 4. Clonal cell lineage involvement in myelodysplastic syndromes studied by fluorescence in situ hybridization and morphology.
    Bernell P, Jacobsson B, Nordgren A, Hast R.
    Leukemia; 1996 Apr 15; 10(4):662-8. PubMed ID: 8618444
    [Abstract] [Full Text] [Related]

  • 5. Myelodysplastic syndromes: the pediatric point of view.
    Locatelli F, Zecca M, Pession A, Maserati E, De Stefano P, Severi F.
    Haematologica; 1995 Apr 15; 80(3):268-79. PubMed ID: 7672722
    [Abstract] [Full Text] [Related]

  • 6. Conventional and molecular cytogenetic features of myelodysplastic syndrome in China.
    Chen L, Li J, Zhu Y, Qiu H, Pan J, Wang R, Qian S, Xu W, Xue Y.
    Exp Oncol; 2007 Dec 15; 29(4):299-303. PubMed ID: 18199987
    [Abstract] [Full Text] [Related]

  • 7. Myelodysplastic syndromes and acute myeloid leukemia with 17p deletion. An entity characterized by specific dysgranulopoïesis and a high incidence of P53 mutations.
    Lai JL, Preudhomme C, Zandecki M, Flactif M, Vanrumbeke M, Lepelley P, Wattel E, Fenaux P.
    Leukemia; 1995 Mar 15; 9(3):370-81. PubMed ID: 7885035
    [Abstract] [Full Text] [Related]

  • 8. Consecutive chromosomal studies in patients with myelodysplastic syndrome (MDS). Czechoslovak MDS Cooperative Group.
    Michalova K, Musilova J, Zemanova Z.
    Ann Genet; 1991 Mar 15; 34(3-4):212-8. PubMed ID: 1809229
    [Abstract] [Full Text] [Related]

  • 9. [Study on the transformation from myelodysplastic syndromes into acute leukemias].
    Shi J, Shao Z, Liu H, Li K, Song L, Zhang Y, Zheng Y, Chen G, Chu Y, He H, Zhao M, He G, Feng B, Hao Y, Yang T, Yang C.
    Zhonghua Xue Ye Xue Za Zhi; 2001 Jul 15; 22(7):351-4. PubMed ID: 11877096
    [Abstract] [Full Text] [Related]

  • 10. Translocation (3;8)(q26;q24): a recurrent chromosomal abnormality in myelodysplastic syndrome and acute myeloid leukemia.
    Lin P, Medeiros LJ, Yin CC, Abruzzo LV.
    Cancer Genet Cytogenet; 2006 Apr 01; 166(1):82-5. PubMed ID: 16616115
    [Abstract] [Full Text] [Related]

  • 11. Redefining monosomy 5 by molecular cytogenetics in 23 patients with MDS/AML.
    Herry A, Douet-Guilbert N, Morel F, Le Bris MJ, De Braekeleer M.
    Eur J Haematol; 2007 Jun 01; 78(6):457-67. PubMed ID: 17391336
    [Abstract] [Full Text] [Related]

  • 12. Childhood myelodysplasia: suggested classification as myelodysplastic syndromes based on laboratory and clinical findings.
    Brandwein JM, Horsman DE, Eaves AC, Eaves CJ, Massing BG, Wadsworth LD, Rogers PC, Kalousek DK.
    Am J Pediatr Hematol Oncol; 1990 Jun 01; 12(1):63-70. PubMed ID: 2309981
    [Abstract] [Full Text] [Related]

  • 13. Myelodysplastic syndrome, juvenile myelomonocytic leukemia, and acute myeloid leukemia associated with complete or partial monosomy 7. European Working Group on MDS in Childhood (EWOG-MDS).
    Hasle H, Aricò M, Basso G, Biondi A, Cantù Rajnoldi A, Creutzig U, Fenu S, Fonatsch C, Haas OA, Harbott J, Kardos G, Kerndrup G, Mann G, Niemeyer CM, Ptoszkova H, Ritter J, Slater R, Starý J, Stollmann-Gibbels B, Testi AM, van Wering ER, Zimmermann M.
    Leukemia; 1999 Mar 01; 13(3):376-85. PubMed ID: 10086728
    [Abstract] [Full Text] [Related]

  • 14. RAS, FLT3, and TP53 mutations in therapy-related myeloid malignancies with abnormalities of chromosomes 5 and 7.
    Side LE, Curtiss NP, Teel K, Kratz C, Wang PW, Larson RA, Le Beau MM, Shannon KM.
    Genes Chromosomes Cancer; 2004 Mar 01; 39(3):217-23. PubMed ID: 14732923
    [Abstract] [Full Text] [Related]

  • 15. Therapy-related myelodysplastic syndrome with monosomy 5 after successful treatment of acute myeloid leukemia (M2).
    Ogasawara T, Yasuyama M, Kawauchi K.
    Am J Hematol; 2005 Jun 01; 79(2):136-41. PubMed ID: 15929101
    [Abstract] [Full Text] [Related]

  • 16. Chromosomal aberrations in bone marrow mesenchymal stroma cells from patients with myelodysplastic syndrome and acute myeloblastic leukemia.
    Blau O, Hofmann WK, Baldus CD, Thiel G, Serbent V, Schümann E, Thiel E, Blau IW.
    Exp Hematol; 2007 Feb 01; 35(2):221-9. PubMed ID: 17258071
    [Abstract] [Full Text] [Related]

  • 17. Therapy may unmask hypoplastic myelodysplastic syndrome that mimics aplastic anemia.
    Konoplev S, Medeiros LJ, Lennon PA, Prajapati S, Kanungo A, Lin P.
    Cancer; 2007 Oct 01; 110(7):1520-6. PubMed ID: 17701956
    [Abstract] [Full Text] [Related]

  • 18. Myelodysplastic syndrome in children and adolescents.
    Niemeyer CM, Baumann I.
    Semin Hematol; 2008 Jan 01; 45(1):60-70. PubMed ID: 18179970
    [Abstract] [Full Text] [Related]

  • 19. Does monosomy 5 really exist in myelodysplastic syndromes and acute myeloid leukemia?
    Galván AB, Mallo M, Arenillas L, Salido M, Espinet B, Pedro C, Florensa L, Serrano S, Solé F.
    Leuk Res; 2010 Sep 01; 34(9):1242-5. PubMed ID: 20362335
    [Abstract] [Full Text] [Related]

  • 20. Familial platelet disorder with propensity to acute myelogenous leukemia: genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies.
    Minelli A, Maserati E, Rossi G, Bernardo ME, De Stefano P, Cecchini MP, Valli R, Albano V, Pierani P, Leszl A, Sainati L, Lo Curto F, Danesino C, Locatelli F, Pasquali F.
    Genes Chromosomes Cancer; 2004 Jul 01; 40(3):165-71. PubMed ID: 15138996
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 34.