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  1. Book: New findings on inhibitor development: from registries to clinical studies

    Peyvandi, Flora / Makris, Michael

    (Haemophilia ; volume 23, supplement 1 (January 2017))

    2017  

    Author's details guest editors: F. Peyvandi, M. Makris
    Series title Haemophilia ; volume 23, supplement 1 (January 2017)
    Collection
    Language English
    Size 13 Seiten, Diagramme
    Publisher Wiley Blackwell
    Publishing place Oxford, UK
    Publishing country Great Britain
    Document type Book
    HBZ-ID HT019283851
    Database Catalogue ZB MED Medicine, Health

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    In stock of ZB MED Cologne/Königswinter

    Shelf markLoan statusLocation
    Zs A 4249 -23,Suppl.1- not available for loan Zeitschriften-Lesesaal

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  2. Article ; Online: ISTH's new strategic plan 2024-2028: A transformative journey toward shaping the future of thrombosis and hemostasis.

    Peyvandi, Flora / Angchaisuksiri, Pantep / Reiser, Thomas

    Journal of thrombosis and haemostasis : JTH

    2024  

    Language English
    Publishing date 2024-04-25
    Publishing country England
    Document type Editorial
    ZDB-ID 2112661-6
    ISSN 1538-7836 ; 1538-7933
    ISSN (online) 1538-7836
    ISSN 1538-7933
    DOI 10.1016/j.jtha.2024.04.013
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Laboratory Testing for von Willebrand Factor Activity by a Glycoprotein Ib-Binding Assay (VWF:GPIbR): HemosIL von Willebrand Factor Ristocetin Cofactor Activity on ACL TOP

    Seidizadeh, Omid / Peyvandi, Flora

    Methods in molecular biology (Clifton, N.J.)

    2023  Volume 2663, Page(s) 669–677

    Abstract: von Willebrand disease (VWD) is a lifelong and common inherited bleeding disorder caused by a quantitative deficiency and/or qualitative defect of von Willebrand factor (VWF). In order to establish the correct diagnosis of VWD, various tests must be ... ...

    Abstract von Willebrand disease (VWD) is a lifelong and common inherited bleeding disorder caused by a quantitative deficiency and/or qualitative defect of von Willebrand factor (VWF). In order to establish the correct diagnosis of VWD, various tests must be conducted, including evaluation of factor VIII activity (FVIII:C), VWF antigen (VWF:Ag), and VWF functional activity. The platelet-dependent VWF activity is measured in different ways, with the historical ristocetin cofactor assay (VWF:RCo) using platelet aggregometry now replaced with newer assays that offer better precision, lower limits of detection, low coefficient of variation, and are fully automated. The VWF activity by glycoprotein Ib-binding assays (VWF:GPIbR) measured on the ACL TOP
    MeSH term(s) Humans ; von Willebrand Factor ; Platelet Glycoprotein GPIb-IX Complex ; von Willebrand Diseases/diagnosis ; Blood Coagulation Tests ; Sensitivity and Specificity
    Chemical Substances von Willebrand Factor ; Platelet Glycoprotein GPIb-IX Complex
    Language English
    Publishing date 2023-05-18
    Publishing country United States
    Document type Journal Article
    ISSN 1940-6029
    ISSN (online) 1940-6029
    DOI 10.1007/978-1-0716-3175-1_44
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  4. Article ; Online: Ultrasound evaluation of hemophilic arthropathy: a proposal of definitions in a changing landscape.

    Gualtierotti, Roberta / Solimeno, Luigi Piero / Peyvandi, Flora

    Research and practice in thrombosis and haemostasis

    2024  Volume 8, Issue 1, Page(s) 102314

    Abstract: The advent of novel effective treatments and the identification of the need to achieve a higher trough level for persons with hemophilia A and B have changed the landscape of management of these patients, allowing to change the target from survival and ... ...

    Abstract The advent of novel effective treatments and the identification of the need to achieve a higher trough level for persons with hemophilia A and B have changed the landscape of management of these patients, allowing to change the target from survival and prevention of life-threatening complications to prevention of musculoskeletal complications and improvement of quality of life. Point-of-care musculoskeletal ultrasound imaging has also improved the early recognition of joint bleeding and the differential diagnosis of acute joint pain. In addition, joint ultrasound allows the evaluation of the severity of hemophilic arthropathy in terms of synovitis and cartilage and bone damage. However, a lack of standardization in the definition of ultrasound elementary lesions of hemophilic arthropathy may lead to confusion and an incorrect evaluation of the presence and progression of joint damage. Here, we propose to start a standardization and validation process for ultrasound definitions of hemophilic arthropathy that has been planned to become a project within the Factor VIII/IX Standardization Subcommittee of the International Society on Thrombosis and Haemostasis Scientific and Standardization Committee.
    Language English
    Publishing date 2024-01-03
    Publishing country United States
    Document type Editorial
    ISSN 2475-0379
    ISSN (online) 2475-0379
    DOI 10.1016/j.rpth.2023.102314
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  5. Article ; Online: Phase 3 study of recombinant von Willebrand factor in patients with severe von Willebrand disease who are undergoing elective surgery: Reply.

    Peyvandi, Flora

    Journal of thrombosis and haemostasis : JTH

    2019  Volume 17, Issue 8, Page(s) 1405–1406

    MeSH term(s) Elective Surgical Procedures ; Factor VIII ; Humans ; von Willebrand Diseases ; von Willebrand Factor
    Chemical Substances von Willebrand Factor ; Factor VIII (9001-27-8)
    Language English
    Publishing date 2019-09-08
    Publishing country England
    Document type Letter ; Comment
    ZDB-ID 2112661-6
    ISSN 1538-7836 ; 1538-7933
    ISSN (online) 1538-7836
    ISSN 1538-7933
    DOI 10.1111/jth.14545
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  6. Article ; Online: ISTH Biennial Impact Report: Looking back and looking forward.

    Weitz, Jeffrey I / Peyvandi, Flora

    Journal of thrombosis and haemostasis : JTH

    2022  Volume 20, Issue 7, Page(s) 1515–1517

    Language English
    Publishing date 2022-07-11
    Publishing country England
    Document type Editorial
    ZDB-ID 2112661-6
    ISSN 1538-7836 ; 1538-7933
    ISSN (online) 1538-7836
    ISSN 1538-7933
    DOI 10.1111/jth.15749
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  7. Article ; Online: "Liver-related aspects of gene therapy for hemophilia: need for collaborations with hepatologists": reply.

    Miesbach, Wolfgang / Foster, Graham R / Peyvandi, Flora

    Journal of thrombosis and haemostasis : JTH

    2023  Volume 21, Issue 8, Page(s) 2307–2308

    Language English
    Publishing date 2023-07-17
    Publishing country England
    Document type Letter ; Comment
    ZDB-ID 2112661-6
    ISSN 1538-7836 ; 1538-7933
    ISSN (online) 1538-7836
    ISSN 1538-7933
    DOI 10.1016/j.jtha.2023.04.030
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Air pollution and cardiovascular health in Middle East and North Africa: many shadows but some light.

    Mannucci, Pier Mannuccio / Peyvandi, Flora

    European journal of preventive cardiology

    2022  Volume 30, Issue 3, Page(s) 254–255

    MeSH term(s) Humans ; Cardiovascular Diseases/diagnosis ; Cardiovascular Diseases/epidemiology ; Particulate Matter/adverse effects ; Global Burden of Disease ; Middle East/epidemiology ; Africa, Northern/epidemiology ; Air Pollution/adverse effects
    Chemical Substances Particulate Matter
    Language English
    Publishing date 2022-11-10
    Publishing country England
    Document type Editorial ; Comment
    ZDB-ID 2626011-6
    ISSN 2047-4881 ; 2047-4873
    ISSN (online) 2047-4881
    ISSN 2047-4873
    DOI 10.1093/eurjpc/zwac292
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  9. Article ; Online: Fitusiran in haemophilia: a breakthrough drug with many unknowns.

    Peyvandi, Flora / Garagiola, Isabella / Abbattista, Maria

    Lancet (London, England)

    2023  Volume 401, Issue 10386, Page(s) 1400–1401

    MeSH term(s) Humans ; Hemophilia A/complications ; Hemophilia A/drug therapy ; Hemophilia B ; Acetylgalactosamine ; RNA, Small Interfering ; Factor VIII
    Chemical Substances fitusiran ; Acetylgalactosamine (KM15WK8O5T) ; RNA, Small Interfering ; Factor VIII (9001-27-8)
    Language English
    Publishing date 2023-03-29
    Publishing country England
    Document type Journal Article ; Comment
    ZDB-ID 3306-6
    ISSN 1474-547X ; 0023-7507 ; 0140-6736
    ISSN (online) 1474-547X
    ISSN 0023-7507 ; 0140-6736
    DOI 10.1016/S0140-6736(23)00514-7
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  10. Article ; Online: "Liver-related aspects of gene therapy for hemophilia: need for collaborations with hepatologists": reply.

    Miesbach, Wolfgang / Foster, Graham R / Peyvandi, Flora

    Journal of thrombosis and haemostasis : JTH

    2023  Volume 21, Issue 7, Page(s) 2000–2001

    MeSH term(s) Humans ; Gastroenterologists ; Hemophilia A/genetics ; Hemophilia A/therapy ; Liver ; Liver Transplantation ; Genetic Therapy/adverse effects ; Hemophilia B/genetics ; Genetic Vectors
    Language English
    Publishing date 2023-06-15
    Publishing country England
    Document type Letter ; Comment
    ZDB-ID 2112661-6
    ISSN 1538-7836 ; 1538-7933
    ISSN (online) 1538-7836
    ISSN 1538-7933
    DOI 10.1016/j.jtha.2023.04.011
    Database MEDical Literature Analysis and Retrieval System OnLINE

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