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  1. Article: Six-Year, Real-World Use of Prophylaxis with Recombinant Factor IX-Albumin Fusion Protein (rIX-FP) in Persons with Hemophilia B: A Single-Center Retrospective-Prospective Study.

    Coppola, Antonio / Rivolta, Gianna Franca / Quintavalle, Gabriele / Matichecchia, Annalisa / Riccardi, Federica / Rossi, Rossana / Benegiamo, Anna / Ranalli, Paola / Coluccio, Valeria / Tagliaferri, Annarita

    Journal of clinical medicine

    2024  Volume 13, Issue 5

    Abstract: ... ...

    Abstract Background
    Language English
    Publishing date 2024-03-06
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2662592-1
    ISSN 2077-0383
    ISSN 2077-0383
    DOI 10.3390/jcm13051518
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Confronting COVID-19: Issues in Hemophilia and Congenital Bleeding Disorders.

    Coppola, Antonio / Tagliaferri, Annarita / Rivolta, Gianna Franca / Quintavalle, Gabriele / Franchini, Massimo

    Seminars in thrombosis and hemostasis

    2020  Volume 46, Issue 7, Page(s) 819–822

    MeSH term(s) Anti-Inflammatory Agents, Non-Steroidal/adverse effects ; Antibodies, Bispecific/therapeutic use ; Antibodies, Monoclonal, Humanized/therapeutic use ; Betacoronavirus ; COVID-19 ; Clinical Trials as Topic ; Comorbidity ; Continuity of Patient Care ; Contraindications, Drug ; Coronavirus Infections/blood ; Coronavirus Infections/complications ; Coronavirus Infections/epidemiology ; Coronavirus Infections/prevention & control ; Delivery of Health Care ; Disease Management ; Drug Substitution ; Factor IX/supply & distribution ; Factor IX/therapeutic use ; Factor VIII/supply & distribution ; Factor VIII/therapeutic use ; Fibrinolytic Agents/adverse effects ; Fibrinolytic Agents/therapeutic use ; Genetic Therapy ; Health Resources/supply & distribution ; Hemophilia A/complications ; Hemophilia A/epidemiology ; Hemophilia A/therapy ; Hemophilia B/complications ; Hemophilia B/epidemiology ; Hemophilia B/therapy ; Hemorrhage/etiology ; Hemorrhage/prevention & control ; Humans ; Pandemics/prevention & control ; Pneumonia, Viral/blood ; Pneumonia, Viral/complications ; Pneumonia, Viral/epidemiology ; Pneumonia, Viral/prevention & control ; Professional-Patient Relations ; SARS-CoV-2 ; Social Media ; Telemedicine ; Thrombophilia/etiology
    Chemical Substances Anti-Inflammatory Agents, Non-Steroidal ; Antibodies, Bispecific ; Antibodies, Monoclonal, Humanized ; Fibrinolytic Agents ; emicizumab (7NL2E3F6K3) ; Factor VIII (9001-27-8) ; Factor IX (9001-28-9)
    Keywords covid19
    Language English
    Publishing date 2020-06-08
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 196901-8
    ISSN 1098-9064 ; 0094-6176
    ISSN (online) 1098-9064
    ISSN 0094-6176
    DOI 10.1055/s-0040-1712961
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  3. Article ; Online: Severe bleeding in a patient with factor XIII deficiency and COVID-19.

    Quintavalle, Gabriele / Coppola, Antonio / Ruggieri, Alessandro / Rivolta, Gianna Franca / Fronti, Elisa / Giangregorio, Francesco / Michieletti, Emanuele / Tagliaferri, Annarita

    Haemophilia : the official journal of the World Federation of Hemophilia

    2020  Volume 27, Issue 1, Page(s) e140–e142

    MeSH term(s) COVID-19/blood ; COVID-19/complications ; Factor XIII Deficiency/complications ; Factor XIII Deficiency/virology ; Female ; Hemorrhage/complications ; Hemorrhage/pathology ; Hemorrhage/virology ; Humans ; Middle Aged ; SARS-CoV-2/isolation & purification
    Keywords covid19
    Language English
    Publishing date 2020-06-24
    Publishing country England
    Document type Case Reports ; Letter
    ZDB-ID 1229713-6
    ISSN 1365-2516 ; 1351-8216 ; 1355-0691
    ISSN (online) 1365-2516
    ISSN 1351-8216 ; 1355-0691
    DOI 10.1111/hae.14088
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  4. Article: Confronting COVID-19: Issues in Hemophilia and Congenital Bleeding Disorders

    Coppola, Antonio / Tagliaferri, Annarita / Rivolta, Gianna Franca / Quintavalle, Gabriele / Franchini, Massimo

    Semin. thromb. hemost

    Keywords covid19
    Publisher WHO
    Document type Article
    Note WHO #Covidence: #32512586
    Database COVID19

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  5. Article ; Online: Prevalence of COVID-19 related hospitalizations and mortality in adults aged ≥40 years with haemophilia: A survey from Europe.

    Hermans, Cedric / Astermark, Jan / Carvalho, Manuela / Dolan, Gerry / d'Oiron, Roseline / Fontana, Pierre / Holme, Pål André / Kenet, Gili / Klamroth, Robert / Mancuso, Maria Elisa / Marquardt, Natascha / Nunez, Ramiro / Katsarou, Olga / Pabinger-Fasching, Ingrid / Quintavalle, Gabriele / Rodgers, Ryan / van der Valk, Paul / Windyga, Jerzy / Jimenez Yuste, Victor /
    Preložnik Zupan, Irena

    Haemophilia : the official journal of the World Federation of Hemophilia

    2023  Volume 29, Issue 3, Page(s) 913–916

    MeSH term(s) Adult ; Humans ; Hemophilia A/complications ; Hemophilia A/epidemiology ; Prevalence ; COVID-19/epidemiology ; Europe/epidemiology ; Hospitalization
    Language English
    Publishing date 2023-02-18
    Publishing country England
    Document type Letter
    ZDB-ID 1229713-6
    ISSN 1365-2516 ; 1351-8216 ; 1355-0691
    ISSN (online) 1365-2516
    ISSN 1351-8216 ; 1355-0691
    DOI 10.1111/hae.14761
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  6. Article ; Online: The effect of carriers' reproductive choices and pregnancy history on sporadic severe haemophilia: A 20-year retrospective study through a regional registry.

    Riccardi, Federica / Coppola, Antonio / Rivolta, Gianna Franca / Matichecchia, Annalisa / Quintavalle, Gabriele / Biasoli, Chiara / Valdrè, Lelia / Piscitelli, Lydia / Percesepe, Antonio / Tagliaferri, Annarita

    Haemophilia : the official journal of the World Federation of Hemophilia

    2022  Volume 28, Issue 2, Page(s) 308–315

    Abstract: Introduction: Haemophilias are X-linked inherited bleeding disorders, due to de novo F8/F9 gene variants in 30-50% of cases. The identification of causative variant in index cases (IC) is crucial for genetic counselling in related women. Over the last ... ...

    Abstract Introduction: Haemophilias are X-linked inherited bleeding disorders, due to de novo F8/F9 gene variants in 30-50% of cases. The identification of causative variant in index cases (IC) is crucial for genetic counselling in related women. Over the last 20 years the Emilia-Romagna Regional Haemophilia Registry documented high proportions of sporadic severe haemophilia.
    Aim: To clarify if carriers' reproductive choices influence the sporadic/familial ratio of severe haemophilia.
    Methods: Genetic counselling and genotyping in 221 relatives of severe IC were retrospectively reviewed, retrieving reproductive choices and pregnancy history of childbearing-age carriers from familial and sporadic pedigrees and according to the IC degree of relationship (mothers, daughters, II/other).
    Results: Carriers' identification rates were lower in sporadic women and in other-degree relatives. Among childbearing age women (n = 140), carriers were 37/48 (77%) and 57/92 (62%) of familial and sporadic relatives, respectively. Forty-five/57 sporadic carriers experienced 67 pregnancies, while 21/37 familial carriers had 39 pregnancies (four voluntary terminations), with a significantly higher number of affected sons in the former (40/67 vs. 12/35, P = .025). Prenatal diagnosis was chosen by 40% and 47% of sporadic and familial aware carriers, respectively. Sporadic mothers often avoided further pregnancies (17/38, 45%) after a firstborn affected child, while familial mothers tended to face pregnancies without prenatal approaches (6/10, 60%).
    Conclusion: In this cohort sporadic offspring account for more than 70% of severe haemophilia cases. This increasing proportion is likely to reflect the influence in reproductive choices of awareness of carriers' status, particularly in sporadic mothers, and of prenatal diagnosis options.
    MeSH term(s) Decision Making ; Female ; Hemophilia A/diagnosis ; Hemophilia A/epidemiology ; Hemophilia A/genetics ; Heterozygote ; Humans ; Pregnancy/psychology ; Registries ; Reproductive History ; Retrospective Studies
    Language English
    Publishing date 2022-01-20
    Publishing country England
    Document type Journal Article
    ZDB-ID 1229713-6
    ISSN 1365-2516 ; 1351-8216 ; 1355-0691
    ISSN (online) 1365-2516
    ISSN 1351-8216 ; 1355-0691
    DOI 10.1111/hae.14490
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  7. Article ; Online: Confronting COVID-19

    Coppola, Antonio / Tagliaferri, Annarita / Rivolta, Gianna Franca / Quintavalle, Gabriele / Franchini, Massimo

    Seminars in Thrombosis and Hemostasis

    Issues in Hemophilia and Congenital Bleeding Disorders

    2020  Volume 46, Issue 07, Page(s) 819–822

    Keywords Hematology ; Cardiology and Cardiovascular Medicine ; covid19
    Language English
    Publisher Georg Thieme Verlag KG
    Publishing country de
    Document type Article ; Online
    ZDB-ID 196901-8
    ISSN 1098-9064 ; 0094-6176
    ISSN (online) 1098-9064
    ISSN 0094-6176
    DOI 10.1055/s-0040-1712961
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  8. Article: Confronting COVID-19: Issues in Hemophilia and Congenital Bleeding Disorders

    Coppola, Antonio / Tagliaferri, Annarita / Rivolta, Gianna Franca / Quintavalle, Gabriele / Franchini, Massimo

    Seminars in Thrombosis and Hemostasis

    (Maintaining Hemostasis and Preventing Thrombosis in COVID-19—Part I)

    2020  Volume 46, Issue 07, Page(s) 819–822

    Series title Maintaining Hemostasis and Preventing Thrombosis in COVID-19—Part I
    Language English
    Publishing date 2020-06-08
    Publisher Thieme Medical Publishers
    Publishing place Stuttgart ; New York
    Document type Article
    ZDB-ID 196901-8
    ISSN 1098-9064 ; 0094-6176
    ISSN (online) 1098-9064
    ISSN 0094-6176
    DOI 10.1055/s-0040-1712961
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  9. Article ; Online: Acquired Factor VII Deficiency Associated with Bronchogenic Carcinoma: A Case Report.

    Franchini, Massimo / Bezzi, Michela / Spreafico, Fabio / Glingani, Claudia / Beccaria, Massimiliano / Greco, Graziana Francesca / Inglese, Francesco / Caruso, Beatrice / Terenziani, Isabella / Quintavalle, Gabriele / De Donno, Giuseppe

    Seminars in thrombosis and hemostasis

    2021  Volume 47, Issue 8, Page(s) 992–994

    MeSH term(s) Carcinoma, Bronchogenic/complications ; Carcinoma, Bronchogenic/diagnosis ; Factor VII ; Factor VII Deficiency/complications ; Factor VII Deficiency/diagnosis ; Humans ; Lung Neoplasms/diagnosis
    Chemical Substances Factor VII (9001-25-6)
    Language English
    Publishing date 2021-07-12
    Publishing country United States
    Document type Case Reports ; Journal Article
    ZDB-ID 196901-8
    ISSN 1098-9064 ; 0094-6176
    ISSN (online) 1098-9064
    ISSN 0094-6176
    DOI 10.1055/s-0041-1726340
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  10. Article ; Online: Inhibitors in Hemophilia B.

    Santoro, Cristina / Quintavalle, Gabriele / Castaman, Giancarlo / Baldacci, Erminia / Ferretti, Antonietta / Riccardi, Federica / Tagliaferri, Annarita

    Seminars in thrombosis and hemostasis

    2018  Volume 44, Issue 6, Page(s) 578–589

    Abstract: Hemophilia B (HB) is an X-linked bleeding disorder caused by deficiency of factor IX (FIX). Patients with the severe form (FIX <1%) account approximately for 30 to 45% of persons with HB and usually suffer from recurrent joint, soft-tissue, and muscle ... ...

    Abstract Hemophilia B (HB) is an X-linked bleeding disorder caused by deficiency of factor IX (FIX). Patients with the severe form (FIX <1%) account approximately for 30 to 45% of persons with HB and usually suffer from recurrent joint, soft-tissue, and muscle bleeds. The availability of safe plasma-derived and recombinant products has virtually abolished the risk of viral infections and the adoption of prophylactic regimens has attenuated the impact of hemophilic arthropathy. Therefore, the development of an inhibitor against FIX is currently the most serious complication that can still occur in the new generations of HB patients. The development of an inhibitor in HB is a rare event (1.5-3% of all patients) but is associated with a significant morbidity, related not only to the bleeding risk but also to the frequent occurrence of allergic/anaphylactic reactions and nephrotic syndrome. Due to the relative rarity of this event, few data exist about risk factors, pathophysiology, and clinical aspects of inhibitors in HB. The induction of immune tolerance is often unsuccessful and can be otherwise affected by many complications in patients with history of allergy or anaphylaxis. Therefore, alternative therapeutic strategies and new approaches are developing. The aim of this narrative review is to discuss current knowledge about risk factors, pathophysiology, and clinical aspects of this rare but serious complication.
    MeSH term(s) Factor IX/pharmacology ; Factor IX/therapeutic use ; Hemophilia B/drug therapy ; Humans
    Chemical Substances Factor IX (9001-28-9)
    Language English
    Publishing date 2018-06-20
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 196901-8
    ISSN 1098-9064 ; 0094-6176
    ISSN (online) 1098-9064
    ISSN 0094-6176
    DOI 10.1055/s-0038-1660817
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