Hasil Pencarian - T. Haferlach

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  1. 1
    Methods to detect minimal residual disease

    Methods to detect minimal residual disease oleh Torsten Haferlach

    Diterbitkan 2018-06-01
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  2. 2
    The time has come for next-generation sequencing in routine diagnostic workup in hematology

    The time has come for next-generation sequencing in routine diagnostic workup in hematology oleh Torsten Haferlach

    Diterbitkan 2021-03-01
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  3. 3
    Advancing leukemia diagnostics: Role of Next Generation Sequencing (NGS) in acute myeloid leukemia

    Advancing leukemia diagnostics: Role of Next Generation Sequencing (NGS) in acute myeloid leukemia oleh Torsten Haferlach

    Diterbitkan 2020-09-01
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  4. 4
    Molecular analysis of myelodysplastic syndrome with isolated deletion of the long arm of chromosome 5 reveals a specific spectrum of molecular mutations with prognostic impact: a study on 123 patients and 27 genes

    Molecular analysis of myelodysplastic syndrome with isolated deletion of the long arm of chromosome 5 reveals a specific spectrum of molecular mutations with prognostic impact: a s... oleh Manja Meggendorfer, Claudia Haferlach, Wolfgang Kern, Torsten Haferlach

    Diterbitkan 2017-09-01
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  5. 5
    Detection of <I>ABL1</I> kinase domain mutations in therapy-naïve <I>BCR-ABL1</I>-positive acute lymphoblastic leukemia

    Detection of <I>ABL1</I> kinase domain mutations in therapy-naïve <I>BCR-ABL1</I>-positive acute lymphoblastic leukemia oleh Constance Baer, Manja Meggendorfer, Claudia Haferlach, Wolfgang Kern, Torsten Haferlach

    Diterbitkan 2021-11-01
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  6. 6
    Molecular landscape of acute promyelocytic leukemia at diagnosis and relapse

    Molecular landscape of acute promyelocytic leukemia at diagnosis and relapse oleh Annette Fasan, Claudia Haferlach, Karolina Perglerovà, Wolfgang Kern, Torsten Haferlach

    Diterbitkan 2017-06-01
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  7. 7
    Serial assessment of suspected myelodysplastic syndromes: significance of flow cytometric findings validated by cytomorphology, cytogenetics, and molecular genetics

    Serial assessment of suspected myelodysplastic syndromes: significance of flow cytometric findings validated by cytomorphology, cytogenetics, and molecular genetics oleh Wolfgang Kern, Claudia Haferlach, Susanne Schnittger, Tamara Alpermann, Torsten Haferlach

    Diterbitkan 2013-02-01
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  8. 8
    Molecular genetic characterization of myeloid/lymphoid neoplasms associated with eosinophilia and rearrangement of PDGFRA, PDGFRB, FGFR1 or PCM1-JAK2

    Molecular genetic characterization of myeloid/lymphoid neoplasms associated with eosinophilia and rearrangement of PDGFRA, PDGFRB, FGFR1 or PCM1-JAK2 oleh Constance Baer, Verena Muehlbacher, Wolfgang Kern, Claudia Haferlach, Torsten Haferlach

    Diterbitkan 2018-08-01
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  9. 9
    The mutational landscape of 18 investigated genes clearly separates four subtypes of myelodysplastic/myeloproliferative neoplasms

    The mutational landscape of 18 investigated genes clearly separates four subtypes of myelodysplastic/myeloproliferative neoplasms oleh Manja Meggendorfer, Sabine Jeromin, Claudia Haferlach, Wolfgang Kern, Torsten Haferlach

    Diterbitkan 2018-05-01
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  10. 10
    A comparative study of molecular mutations in 381 patients with myelodysplastic syndrome and in 4130 patients with acute myeloid leukemia

    A comparative study of molecular mutations in 381 patients with myelodysplastic syndrome and in 4130 patients with acute myeloid leukemia oleh Ulrike Bacher, Torsten Haferlach, Wolfgang Kern, Claudia Haferlach, Susanne Schnittger

    Diterbitkan 2007-06-01
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  11. 11
    Acute myeloid leukemia

    Acute myeloid leukemia oleh Torsten Haferlach, (Coordinating Author)

    Diterbitkan 2019-06-01
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  12. 12
    The benefit of population-based studies for older patients with acute myeloid leukemia

    The benefit of population-based studies for older patients with acute myeloid leukemia oleh Ulrike Bacher, Torsten Haferlach

    Diterbitkan 2012-12-01
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  13. 13
    Detection and characterization of homozygosity of mutated CALR by copy neutral loss of heterozygosity in myeloproliferative neoplasms among cases with high CALR mutation loads or with progressive disease

    Detection and characterization of homozygosity of mutated CALR by copy neutral loss of heterozygosity in myeloproliferative neoplasms among cases with high CALR mutation loads or w... oleh Anna Stengel, Sabine Jeromin, Torsten Haferlach, Manja Meggendorfer, Wolfgang Kern, Claudia Haferlach

    Diterbitkan 2019-05-01
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  14. 14
    Clinical impact of FLT3 mutation load in acute promyelocytic leukemia with t(15;17)/PML-RARA

    Clinical impact of FLT3 mutation load in acute promyelocytic leukemia with t(15;17)/PML-RARA oleh Susanne Schnittger, Ulrike Bacher, Claudia Haferlach, Wolfgang Kern, Tamara Alpermann, Torsten Haferlach

    Diterbitkan 2011-12-01
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  15. 15
    Comparison of genetic and clinical aspects in patients with acute myeloid leukemia and myelodysplastic syndromes all with more than 50% of bone marrow erythropoietic cells

    Comparison of genetic and clinical aspects in patients with acute myeloid leukemia and myelodysplastic syndromes all with more than 50% of bone marrow erythropoietic cells oleh Ulrike Bacher, Claudia Haferlach, Tamara Alpermann, Wolfgang Kern, Susanne Schnittger, Torsten Haferlach

    Diterbitkan 2011-09-01
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  16. 16
    Mutations of JAK2 and TET2, but not CBL are detectable in a high portion of patients with refractory anemia with ring sideroblasts and thrombocytosis

    Mutations of JAK2 and TET2, but not CBL are detectable in a high portion of patients with refractory anemia with ring sideroblasts and thrombocytosis oleh Johanna Flach, Frank Dicker, Susanne Schnittger, Alexander Kohlmann, Torsten Haferlach, Claudia Haferlach

    Diterbitkan 2010-03-01
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  17. 17
    Acute myeloid leukemias with ring sideroblasts show a unique molecular signature straddling secondary acute myeloid leukemia and de novo acute myeloid leukemia

    Acute myeloid leukemias with ring sideroblasts show a unique molecular signature straddling secondary acute myeloid leukemia and de novo acute myeloid leukemia oleh Pedro Martin-Cabrera, Sabine Jeromin, Karolína Perglerovà, Claudia Haferlach, Wolfgang Kern, Torsten Haferlach

    Diterbitkan 2017-04-01
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  18. 18
    Should clinical hematologists put their microscopes on eBay?

    Should clinical hematologists put their microscopes on eBay? oleh Mars van’t Veer, Torsten Haferlach

    Diterbitkan 2014-10-01
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  19. 19
    Answer to Comment on the Editorial ‘Should hematologists put there microscopes on eBay?’

    Answer to Comment on the Editorial ‘Should hematologists put there microscopes on eBay?’ oleh Mars van ‘t Veer, Torsten Haferlach

    Diterbitkan 2015-01-01
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  20. 20
    Molecular characterization of AML with RUNX1-RUNX1T1 at diagnosis and relapse reveals net loss of co-mutations

    Molecular characterization of AML with RUNX1-RUNX1T1 at diagnosis and relapse reveals net loss of co-mutations oleh Alexander Höllein, Niroshan Nadarajah, Manja Meggendorfer, Sabine Jeromin, Wolfgang Kern, Claudia Haferlach, Torsten Haferlach

    Diterbitkan 2019-02-01
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