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  1. Book: Congenital and acquired disorders of macrophages and histiocytes

    Berliner, Nancy

    (Hematology, oncology clinics of North America ; 29,5)

    2015  

    Author's details ed. Nancy Berliner
    Series title Hematology, oncology clinics of North America ; 29,5
    Collection
    Language English
    Size XV S., S. 800 - 970 : Ill., graph. Darst.
    Publisher Elsevier
    Publishing place Philadelphia, Pa. u.a.
    Publishing country United States
    Document type Book
    HBZ-ID HT018821457
    ISBN 978-0-323-40088-6 ; 0-323-40088-4
    Database Catalogue ZB MED Medicine, Health

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  2. Article ; Online: The demise of Roe v Wade: a hematologist's perspective.

    Berliner, Nancy

    Blood

    2022  Volume 140, Issue 14, Page(s) 1573–1574

    Language English
    Publishing date 2022-08-15
    Publishing country United States
    Document type Editorial
    ZDB-ID 80069-7
    ISSN 1528-0020 ; 0006-4971
    ISSN (online) 1528-0020
    ISSN 0006-4971
    DOI 10.1182/blood.2022018163
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Book: Immunodeficiency, infection, and stem cell transplantation

    Berliner, Nancy

    (Hematology oncology clincis of North America ; 25,1)

    2011  

    Author's details guest ed. Nancy Berliner
    Series title Hematology oncology clincis of North America ; 25,1
    Hematology, oncology clinics of North America
    Collection Hematology, oncology clinics of North America
    Language English
    Size XI, 240 S.
    Publisher Saunders an imprint of Elsevier
    Publishing place Philadelphia, Pa
    Publishing country United States
    Document type Book
    HBZ-ID HT016874441
    ISBN 978-1-4557-0633-4 ; 1-4557-0633-7
    Database Catalogue ZB MED Medicine, Health

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  4. Book: Anemia

    Benz, Edward J. / Berliner, Nancy / Schiffman, Fred J.

    pathophysiology, diagnosis and management

    (Cambridge medicine)

    2018  

    Author's details edited by Edward J. Benz, Jr., Nancy Berliner, Fred J. Schiffman
    Series title Cambridge medicine
    Keywords Anemia
    Language English
    Size xii, 242 Seiten, Illustrationen
    Publisher Cambridge University Press
    Publishing place Cambridge
    Publishing country Great Britain
    Document type Book
    Note Zugang zu Online-Ausgabe über Code, Includes bibliographical references and index
    HBZ-ID HT019772992
    ISBN 978-0-521-51426-2 ; 978-1-108-42520-9 ; 0-521-51426-6 ; 1-108-42520-8
    Database Catalogue ZB MED Medicine, Health

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  5. Article ; Online: Introduction to a review series on COVID-19 and the hematologist.

    Ortel, Thomas L / Berliner, Nancy

    Blood

    2022  Volume 140, Issue 3, Page(s) 163–164

    MeSH term(s) COVID-19 ; Hematology ; Humans
    Language English
    Publishing date 2022-06-02
    Publishing country United States
    Document type Journal Article
    ZDB-ID 80069-7
    ISSN 1528-0020 ; 0006-4971
    ISSN (online) 1528-0020
    ISSN 0006-4971
    DOI 10.1182/blood.2022017072
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: How I manage inpatient consultations for quantitative neutrophil abnormalities in adults.

    Zon, Rebecca L / Berliner, Nancy

    Blood

    2022  Volume 142, Issue 9, Page(s) 786–793

    Abstract: Neutrophilia and neutropenia commonly lead to inpatient hematology consultation. Quantitative neutrophil abnormalities have a broad differential and include diagnoses that are important to recognize because they may be associated with increased mortality. ...

    Abstract Neutrophilia and neutropenia commonly lead to inpatient hematology consultation. Quantitative neutrophil abnormalities have a broad differential and include diagnoses that are important to recognize because they may be associated with increased mortality. Neutrophilia can reflect etiologies such as infection, medications, inflammation, splenectomy, and congenital disorders. Neutropenia can arise from infection, medications, autoimmune destruction, sequestration, nutritional deficiency, malignancy, and congenital neutropenia syndromes. In the evaluation of all abnormalities of neutrophil number, the timing of the change, and the patient's historical neutrophil count are crucial.
    MeSH term(s) Humans ; Adult ; Neutrophils ; Inpatients ; Neutropenia/diagnosis ; Neutropenia/therapy ; Neutropenia/etiology ; Leukocyte Disorders/diagnosis ; Leukocyte Disorders/therapy ; Leukocytosis/complications ; Referral and Consultation
    Language English
    Publishing date 2022-10-18
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 80069-7
    ISSN 1528-0020 ; 0006-4971
    ISSN (online) 1528-0020
    ISSN 0006-4971
    DOI 10.1182/blood.2021014818
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Changing of the guard…the old and the new.

    Berliner, Nancy / Roberts, Andrew

    Blood

    2020  Volume 135, Issue 1, Page(s) 1

    MeSH term(s) Humans ; Periodicals as Topic ; Publishing/organization & administration
    Language English
    Publishing date 2020-01-02
    Publishing country United States
    Document type Editorial
    ZDB-ID 80069-7
    ISSN 1528-0020 ; 0006-4971
    ISSN (online) 1528-0020
    ISSN 0006-4971
    DOI 10.1182/blood.2019004224
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article: Hemophagocytic lymphohistiocytosis as an etiology of bone marrow failure.

    Paolino, Jonathan / Berliner, Nancy / Degar, Barbara

    Frontiers in oncology

    2022  Volume 12, Page(s) 1016318

    Abstract: Hemophagocytic lymphohistiocytosis (HLH) is a syndrome of multiorgan system dysfunction that is caused by hypercytokinemia and persistent activation of cytotoxic T lymphocytes and macrophages. A nearly ubiquitous finding and a diagnostic criterion of HLH ...

    Abstract Hemophagocytic lymphohistiocytosis (HLH) is a syndrome of multiorgan system dysfunction that is caused by hypercytokinemia and persistent activation of cytotoxic T lymphocytes and macrophages. A nearly ubiquitous finding and a diagnostic criterion of HLH is the presence of cytopenias in ≥ 2 cell lines. The mechanism of cytopenias in HLH is multifactorial but appears to be predominantly driven by suppression of hematopoiesis by pro-inflammatory cytokines and, to some extent, by consumptive hemophagocytosis. Recognition of cytopenias as a manifestation of HLH is an important consideration for patients with bone marrow failure of unclear etiology.
    Language English
    Publishing date 2022-10-27
    Publishing country Switzerland
    Document type Journal Article ; Review
    ZDB-ID 2649216-7
    ISSN 2234-943X
    ISSN 2234-943X
    DOI 10.3389/fonc.2022.1016318
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Introduction to a How I Treat series on hematologic complications in pregnancy.

    Bollard, Catherine / Berliner, Nancy

    Blood

    2020  Volume 136, Issue 19, Page(s) 2093

    MeSH term(s) Disease Management ; Female ; Humans ; Pregnancy ; Pregnancy Complications, Hematologic/therapy
    Keywords covid19
    Language English
    Publishing date 2020-11-04
    Publishing country United States
    Document type Introductory Journal Article
    ZDB-ID 80069-7
    ISSN 1528-0020 ; 0006-4971
    ISSN (online) 1528-0020
    ISSN 0006-4971
    DOI 10.1182/blood.2020008356
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Introduction to a review series on rare systemic hematologic disorders.

    Berliner, Nancy / Sehn, Laurie

    Blood

    2020  Volume 135, Issue 16, Page(s) 1305

    MeSH term(s) Disease Management ; Hematologic Diseases/diagnosis ; Hematologic Diseases/therapy ; Histiocytosis/diagnosis ; Histiocytosis/therapy ; Humans ; Lymphoproliferative Disorders/diagnosis ; Lymphoproliferative Disorders/therapy ; Mastocytosis, Systemic/diagnosis ; Mastocytosis, Systemic/therapy
    Language English
    Publishing date 2020-02-19
    Publishing country United States
    Document type Editorial ; Introductory Journal Article
    ZDB-ID 80069-7
    ISSN 1528-0020 ; 0006-4971
    ISSN (online) 1528-0020
    ISSN 0006-4971
    DOI 10.1182/blood.2019004082
    Database MEDical Literature Analysis and Retrieval System OnLINE

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