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  1. Article: Hematology: the specialty with a record number of new approvals.

    Gavriilaki, Eleni

    Frontiers in medicine

    2024  Volume 11, Page(s) 1385052

    Language English
    Publishing date 2024-02-29
    Publishing country Switzerland
    Document type Editorial
    ZDB-ID 2775999-4
    ISSN 2296-858X
    ISSN 2296-858X
    DOI 10.3389/fmed.2024.1385052
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Editorial: 50 years of BMT: long-term outcomes and late complications after transplantation.

    Gavriilaki, Eleni

    Frontiers in oncology

    2023  Volume 13, Page(s) 1253971

    Language English
    Publishing date 2023-08-01
    Publishing country Switzerland
    Document type Editorial
    ZDB-ID 2649216-7
    ISSN 2234-943X
    ISSN 2234-943X
    DOI 10.3389/fonc.2023.1253971
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Editorial: Women in science - hematology 2023.

    Gavriilaki, Eleni / Huang, Chien-Ling / Nayak, Lalitha

    Frontiers in medicine

    2024  Volume 11, Page(s) 1402357

    Language English
    Publishing date 2024-04-09
    Publishing country Switzerland
    Document type Editorial
    ZDB-ID 2775999-4
    ISSN 2296-858X
    ISSN 2296-858X
    DOI 10.3389/fmed.2024.1402357
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: Editorial: Endotheliopathies: Current concepts and importance in clinical practice.

    Gavriilaki, Eleni / Anyfanti, Panagiota

    Frontiers in medicine

    2023  Volume 10, Page(s) 1162121

    Language English
    Publishing date 2023-03-03
    Publishing country Switzerland
    Document type Editorial
    ZDB-ID 2775999-4
    ISSN 2296-858X
    ISSN 2296-858X
    DOI 10.3389/fmed.2023.1162121
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article: Sickle Cell Disease: Current Understanding and Future Options.

    Varelas, Christos / Gavriilaki, Eleni

    Journal of clinical medicine

    2023  Volume 12, Issue 18

    Abstract: Sickle cell disease (SCD) is a prevalent inherited hemoglobin disorder encompassing a cluster of congenital hemolytic anemias, each distinguished by the prevalence of sickle hemoglobin (HbS) [ ... ]. ...

    Abstract Sickle cell disease (SCD) is a prevalent inherited hemoglobin disorder encompassing a cluster of congenital hemolytic anemias, each distinguished by the prevalence of sickle hemoglobin (HbS) [...].
    Language English
    Publishing date 2023-09-13
    Publishing country Switzerland
    Document type Editorial
    ZDB-ID 2662592-1
    ISSN 2077-0383
    ISSN 2077-0383
    DOI 10.3390/jcm12185943
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Editorial

    Eleni Gavriilaki / Panagiota Anyfanti

    Frontiers in Medicine, Vol

    Endotheliopathies: Current concepts and importance in clinical practice

    2023  Volume 10

    Keywords endotheliopathies ; endothelial dysfunction ; endothelial injury syndromes ; COVID-19 ; hematological disorders ; cardiovascular disorders ; Medicine (General) ; R5-920
    Language English
    Publishing date 2023-03-01T00:00:00Z
    Publisher Frontiers Media S.A.
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  7. Article: The Challenge for a Correct Diagnosis of Refractory Thrombocytopenia: ITP or MDS with Isolated Thrombocytopenia?

    Kosmidou, Aikaterini / Gavriilaki, Eleni / Tragiannidis, Athanasios

    Cancers

    2024  Volume 16, Issue 8

    Abstract: Immune thrombocytopenia (ITP) is an autoimmune disease characterized by isolated thrombocytopenia. It is diagnosed in patients with a platelet count below 100,000 per cubic millimeter in whom other causes of thrombocytopenia have been ruled out, and its ... ...

    Abstract Immune thrombocytopenia (ITP) is an autoimmune disease characterized by isolated thrombocytopenia. It is diagnosed in patients with a platelet count below 100,000 per cubic millimeter in whom other causes of thrombocytopenia have been ruled out, and its diagnosis is generally one of exclusion. Clinical manifestations of patients may vary from asymptomatic disease to mild mucocutaneous or life-threatening bleeding. Glucocorticoids are used as first-line treatment for ITP, while other second-line medications, mainly thrombopoietin-receptor agonists (TPO-RA) and rituximab, are given to patients in whom ITP does not remit, or relapses soon after glucocorticoid treatment. Refractoriness of ITP strongly questions its diagnosis and necessitates a thorough clinical and laboratory work-up to decide whether that is the case of refractory ITP or a misdiagnosis. The aim of this review is to summarize the conditions associated with isolated thrombocytopenia and highlight the characteristics of confusing cases. Even though the case of a myelodysplastic syndrome presented with isolated thrombocytopenia (MDS-IT) is relatively rare and not well-established in the literature, it constitutes one of the most predominant misdiagnoses of refractory ITP. MDS-IT patients are thought to present with multilineage dysplasia, normal karyotype and low risk prognostic score, based on IPSS-R. It has been shown that a significant proportion of MDS-IT patients are misdiagnosed as having the more common ITP. Therefore, it is crucial that in confusing cases of persistent thrombocytopenia a detailed diagnostic work-up is applied-including evaluation of peripheral-blood smear, bone marrow examination and cytogenetic testing-to avoid unnecessary therapy delay.
    Language English
    Publishing date 2024-04-11
    Publishing country Switzerland
    Document type Journal Article ; Review
    ZDB-ID 2527080-1
    ISSN 2072-6694
    ISSN 2072-6694
    DOI 10.3390/cancers16081462
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Sickle Cell Disease

    Christos Varelas / Eleni Gavriilaki

    Journal of Clinical Medicine, Vol 12, Iss 5943, p

    Current Understanding and Future Options

    2023  Volume 5943

    Abstract: Sickle cell disease (SCD) is a prevalent inherited hemoglobin disorder encompassing a cluster of congenital hemolytic anemias, each distinguished by the prevalence of sickle hemoglobin (HbS) [.] ...

    Abstract Sickle cell disease (SCD) is a prevalent inherited hemoglobin disorder encompassing a cluster of congenital hemolytic anemias, each distinguished by the prevalence of sickle hemoglobin (HbS) [.]
    Keywords n/a ; Medicine ; R
    Language English
    Publishing date 2023-09-01T00:00:00Z
    Publisher MDPI AG
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    Full text online

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    Inter-library loan at ZB MED

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  9. Article ; Online: COVID-19 sequelae: can long-term effects be predicted?

    Gavriilaki, Eleni / Kokoris, Styliani

    The Lancet. Infectious diseases

    2022  Volume 22, Issue 12, Page(s) 1651–1652

    MeSH term(s) Humans ; COVID-19 ; Risk Factors ; Disease Progression
    Language English
    Publishing date 2022-08-26
    Publishing country United States
    Document type Journal Article ; Comment
    ZDB-ID 2061641-7
    ISSN 1474-4457 ; 1473-3099
    ISSN (online) 1474-4457
    ISSN 1473-3099
    DOI 10.1016/S1473-3099(22)00529-1
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    In stock of ZB MED Cologne/Königswinter

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    bis Jg. 1994: Bestellungen von Artikeln über das Online-Bestellformular
    Jg. 1995 - 2021: Lesesall (2.OG)
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  10. Article ; Online: "Long COVID-19" of Researchers: What to Do Next?

    Gavriilaki, Eleni / Maiques-Diaz, Alba

    HemaSphere

    2021  Volume 6, Issue 1, Page(s) e673

    Language English
    Publishing date 2021-12-22
    Publishing country United States
    Document type Editorial
    ISSN 2572-9241
    ISSN (online) 2572-9241
    DOI 10.1097/HS9.0000000000000673
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    Inter-library loan at ZB MED

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