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Precision Molecular Pathology of Myeloid Neoplasms 1st Editon 2018 Softbound at Meripustak

Precision Molecular Pathology of Myeloid Neoplasms 1st Editon 2018 Softbound by Chung-Che (Jeff) Chang, Robert S. Ohgami, Springer

Books from same Author: Chung-Che (Jeff) Chang, Robert S. Ohgami

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  • General Information  
    Author(s)Chung-Che (Jeff) Chang, Robert S. Ohgami
    PublisherSpringer
    Edition1st Edition
    ISBN9783319872414
    Pages427
    BindingSoftbound
    LanguageEnglish
    Publish YearAugust 2018

    Description

    Springer Precision Molecular Pathology of Myeloid Neoplasms 1st Editon 2018 Softbound by Chung-Che (Jeff) Chang, Robert S. Ohgami

    This volume provides a comprehensive, state-of-the art review of myeloid neoplasms. The book presents updated information on epidemiology, clinical presentation, morphologic findings, molecular genomic abnormalities, pathogenesis, and target therapies. The text helps to guide accurate diagnosis, the administration of appropriate ancillary molecular tests, patient management, and investigative efforts. The book also includes over 200 illustrations, photographs, and tables. Written by experts in the field, Precision Molecular Pathology of Myeloid Neoplasms serves as a valuable resource for pathologists, hematologists/oncologists, fellows, and researchers in understanding the molecular pathology of myeloid neoplasms. Acute myeloid leukemia (AML) with recurrent cytogenetic abnormalities.- AML with characteristic molecular mutations: RUNX1, CEPA, NPM1, etc.- AML, NOS/AML with dysplasia-related changes/therapy-related myeloid neoplasm.- Myelodysplastic syndromes (MDS).- Chronic myelogenous leukemia (CML).- Polythesemia vera (PV).- Essential thrombocythemia (ET).- Primary myelofibrosis (PMF).- Mastocytosis.- Myeloproliferative neoplasms (MPN), rare types (Chronic eosinophilic leukemia, Chronic neutrophilic leukemia).- Atypical CML.- Chronic myelomonocytic leukemia (CMML).- Juvenile myelomonocytic leukemia (JMML).- Childhood MDS.- Familial AML/MPN/MDS.- Myeloid and lymphoid neoplasm with eosinophilia and abnormalities of PDGFRA, PDGFRB, or FGFR1.



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