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eISSN 2035-3006

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Editor-in-Chief: Giuseppe Leone | Italy

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  • MUTATIONAL PROFILES OF F8 AND F9 IN A COHORT OF HAEMOPHILIA A AND HAEMOPHILIA B PATIENTS IN THE MULTI-ETHNIC MALAYSIAN POPULATION

    Maimiza Zahari, Siti Aishah Sulaiman, Zulhabri Othman, Yasmin Ayob, Faraizah Abd Karim, Rahman Jamal
    e2018056
    2018-09-01
    https://doi.org/10.4084/mjhid.2018.056
    1955
    PDF: 1016
    HTML: 659
    Figure 1: 126
    Figure 2: 143
  • SUCCESSFUL LONG TERM ERADICATION OF FACTOR VIII INHIBITOR IN PATIENTS WITH ACQUIRED HAEMOPHILIA A IN SAUDI ARABIA

    Galila F Zaher, Soheir S Adam
    e2012021
    2012-04-02
    https://doi.org/10.4084/mjhid.2012.021
    1244
    PDF: 872
    HTML: 3575
  • A HEALTH RELATED QUALITY OF LIFE AND PSYCHOPATHOLOGICAL SYMPTOMS IN PEOPLE WITH HEMOPHILIA, BLOODBORNE CO-INFECTIONS AND COMORBIDITIES: AN ITALIAN MULTICENTER OBSERVATIONAL STUDY PSYCHOLOGICAL DINAMICS OF A GROUP OF ITALIAN HEMOPHILIACS WITH AND WITHOUT (CO)INFECTIONS AND COMORBIDITIES: A MULTICENTER STUDY

    Mario Schiavoni, CARLO PRUNETI, SARA GUIDOTTI, ALESSANDRA MOSCATELLO, FRANCESCA GIORDANO, ANTONELLA COLUCCIA, RITA CARLOTTA SANTORO, MARIA FRANCESCA MANSUETO, EZIO ZANON, RENATO MARINO, ISABELLA CANTORI, RAIMONDO DE CRISTOFARO
    e2023005
    2023-01-01
    https://doi.org/10.4084/MJHID.2023.005
    1348
    PDF: 1172
    HTML: 485
  • Guest Editor: G. Castaman AGING WITH HEMOPHILIA: THE CHALLENGE OF APPROPRIATE DRUG PRESCRIPTION Hemophilia and aging

    Pier Mannuccio Mannucci
    e2019056
    2019-08-29
    https://doi.org/10.4084/mjhid.2019.056
    1593
    PDF: 1406
    HTML: 233
  • Guest Editor: G. Castaman GENE THERAPY FOR HEMOPHILIA: FACTS AND QUANDARIES IN THE 21ST CENTURY GENE THERAPY FOR HEMOPHILIA

    Bhavya S Doshi, Valder R Arruda, Valder R Arruda
    e2020069
    2020-09-08
    https://doi.org/10.4084/mjhid.2020.069
    1946
    PDF: 1816
    HTML: 327
  • CIRCUMCISION IN MALES WITH BLEEDING DISORDERS

    Hassan Mansouritorghabeh, Abdollah Banihashem, Alireza Modaresi, Lida Manavifar
    e2013004
    2013-01-02
    https://doi.org/10.4084/mjhid.2013.004
    1852
    PDF: 859
    HTML: 6745
    Cover letter: 146
  • MOLECULAR MECHANISMS OF INHIBITOR DEVELOPMENT IN HEMOPHILIA Guest Editor: Giancarlo Costaman

    Davide Matino, Paul Tieu, Dr., Antony Chan
    e2020001
    2020-01-01
    https://doi.org/10.4084/mjhid.2020.001
    3053
    PDF: 1562
    HTML: 390
  • DESCRIPTIVE EPIDEMIOLOGY OF HEMOPHILIA AND OTHER COAGULATION DISORDERS IN MANSOURA , EGYPT

    Youssef Al Tonbary, Rasha ElAshry, Maysaa El Sayed Zaki
    e2010025
    2010-08-03
    https://doi.org/10.4084/mjhid.2010.025
    1584
    PDF: 880
    HTML: 926
  • CLINICAL PROFILE OF PATIENTS WITH RARE INHERITED COAGULATION DISORDERS: A RETROSPECTIVE ANALYSIS OF 67 PATIENTS FROM NORTHERN INDIA

    Sanjeev Kumar Sharma, Suman Kumar, Tulika Seth, Pravas Mishra, Narendra Agrawal, Gurmeet Singh, Avinash Singh, Manoranjan Mahapatra, Seema Tyagi, Haraprasad Pati, Renu Saxena
    e2012057
    2012-10-02
    https://doi.org/10.4084/mjhid.2012.057
    1258
    PDF: 530
    HTML: 2899
  • IMPLEMENTATION OF MICROELIMINATION STRATEGY IN ERADICATION OF CHRONIC HEPATITIS C INFECTION IN PATIENTS WITH HEMOPHILIA IN THE NORTHERN REGION OF SERBIA Microelimination Strategy of Chronic Hepatitis C Infection in patients with Hemophilia

    Maja Ružić, Natalija Rajić, Milotka Fabri, Ivana Urošević, Marina Dragičević Jojkić, Tomislav Preveden, Maria Pete, Nebojša Rajić
    e2021058
    2021-08-29
    https://doi.org/10.4084/MJHID.2021.058
    799
    PDF: 308
    HTML: 138
  • ON THE VERSATILITY OF VON WILLEBRAND FACTOR

    Antoine Rauch, Peter Lenting
    e2013046
    2013-07-10
    https://doi.org/10.4084/mjhid.2013.046
    2731
    PDF: 1080
    HTML: 11204
  • Hsa-miR-5581-3p and hsa-miR-542-3p target the F8 gene in hemophilia A without F8 mutations F8 gene is regulated by miRNAs

    Feiying Meng
    e2021041
    2021-06-28
    https://doi.org/10.4084/MJHID.2021.041
    1060
    PDF: 459
    HTML: 211
  • CHANGES OF VON WILLEBRAND FACTOR DURING PREGNANCY IN WOMEN WITHOUT AND WITH VON WILLEBRAND DISEASE

    Giancarlo Castaman
    e2013052
    2013-07-16
    https://doi.org/10.4084/mjhid.2013.052
    2973
    PDF: 1007
    HTML: 8519
  • Correlation to FVIII:C in two thrombin generation tests: TGA-CAT and INNOVANCE ETP

    Marcus Ljungkvist
    e2017064
    2017-11-01
    https://doi.org/10.4084/mjhid.2017.064
    2170
    PDF: 753
    HTML: 845
    Figure 2: 197
    Figure 1: 151
  • PATIENTS REFERRED FOR BLEEDING SYMPTOMS OF UNKNOWN CAUSE: DOES EVALUATION OF THROMBIN GENERATION CONTRIBUTE TO DIAGNOSIS?

    Elena Holm, Eva Zetterberg, Susanna Lövdahl, Erik Berntorp
    e2016014
    2016-02-10
    https://doi.org/10.4084/mjhid.2016.014
    3680
    PDF: 773
    HTML: 1574
  • DISCOVERY OF TYPE 3 VON WILLEBRAND DISEASE IN A COHORT OF PATIENTS WITH SUSPECTED HEMOPHILIA A IN CÔTE D’IVOIRE

    Adia Eusèbe Adjambri, Sylvie Bouvier, Roseline N'guessan, Emma N’draman-Donou, Mireille Yayo-Ayé, Marie-France Meledje, Missa Louis Adjé, Duni Sawadogo
    e2020019
    2020-02-26
    https://doi.org/10.4084/mjhid.2020.019
    1396
    PDF: 1228
    HTML: 217
  • The EVOLVING ROLE OF HAEMATOLOGY NURSING PRACTICE: A CROSS-SECTIONAL SURVEY

    Sarah Liptrott, Mairéad NíChonghaile, Liz O'Connell, Erik Aerts
    e2023033
    2023-04-28
    https://doi.org/10.4084/MJHID.2023.033
    1656
    Suppl. Files: 825
    HTML: 402
    PDF: 702
  • THE ROLE OF BLEEDING HISTORY AND CLINICAL MARKERS FOR THE CORRECT DIAGNOSIS OF VWD

    Alberto Tosetto
    e2013051
    2013-07-12
    https://doi.org/10.4084/mjhid.2013.051
    2290
    PDF: 882
    HTML: 4015
  • MILD BLEEDERS: DIAGNOSIS IS ELUSIVE IN LARGE NUMBER OF PATIENTS

    Mrinalini kotru, Deepti Mutereja, Abhishek Purohit, Seema Tyagi, Manoranjan Mahapatra, Renu Saxena, Hara Prasad Pati
    e2016049
    2016-10-17
    https://doi.org/10.4084/mjhid.2016.049
    3249
    PDF: 688
    HTML: 700
    Figure 1 Distribution of the various causes of mild bleeding (in %) in males and females: 163
    Figure 2 Age and Sex distribution of patients with Bleeding disorders- Unclassified: 159
    Table : Distribution of the sites of bleeding and their causes: 163
  • Acquired Hemophilia A successfully treated with rituximab

    Giovanni D'Arena, Elvira Grandone, Matteo Nicola Dario Di Minno, Pellegrino Musto, Giovanni Di Minno
    e2015024
    2015-02-17
    https://doi.org/10.4084/mjhid.2015.024
    1843
    PDF: 1091
    HTML: 1443
    Figure 1: 151
  • VON WILLEBRAND FACTOR, ANGIODYSPLASIA AND ANGIOGENESIS

    Anna M. Randi, Mike A Laffan, Richard D. Starke
    e2013060
    2013-09-02
    https://doi.org/10.4084/mjhid.2013.060
    3648
    PDF: 1516
    HTML: 8003
    Randi Fig: 159
  • THE USE OF MONOCLONAL ANTIBODIES IN THE TREATMENT OF AUTOIMMUNE COMPLICATIONS OF CHRONIC LYMPHOCYTIC LEUKEMIA

    Luca Laurenti
    e2013027
    2013-04-10
    https://doi.org/10.4084/mjhid.2013.027
    2060
    PDF: 1003
    HTML: 2690
  • CHILDREN IN CORONAVIRUSES’ WONDERLAND: WHAT CLINICIANS NEED TO KNOW Corona virus and Children

    Giuseppe Lassandro, Valentina  Palladino, Anna Amoruso, Viviana Palmieri, Giovanna Russo, Paola Giordano
    e2020042
    2020-06-28
    https://doi.org/10.4084/mjhid.2020.042
    1345
    PDF: 901
    HTML: 288
  • A MULTICENTER ICET-A STUDY ON AGE AT MENARCHE AND MENSTRUAL CYCLES IN PATIENTS WITH TRANSFUSION-DEPENDENT THALASSEMIA (TDT) WHO STARTED EARLY CHELATION THERAPY WITH DIFFERENT CHELATING AGENTS. Age at menarche and menstrual cycles in patients with transfusion-dependent thalassemia.

    SALVATORE DI MAIO, VINCENZO DE SANCTIS, PIERLUIGI MARZUILLO, CHRISTOS KATTAMIS, SHAHINA DAAR, MEHERAN KARIMI, SAKI FOROUGH, ATANAS BANKEV, VALERIA KALEVA, SOTEROULA CHRISTOU, CARMELO FORTUGNO, POLYXENI DELAPORTA, ASHRAF T SOLIMAN , PLOUTARCHOS TZOULIS
    e2023058
    2023-10-30
    https://doi.org/10.4084/MJHID.2023.058
    700
    PDF: 452
    HTML: 91
  • EFFECTS OF FACTOR XIII DEFICIENCY ON THROMBOELASTOGRAPHY. THROMBELASTOGRAPHY WITH CALCIUM AND LYSIS BY ADDITION OF STREPTOKINASE IS MORE SENSITIVE THAN SOLUBILITY TESTS

    Marta E Martinuzzo
    e2016037
    2016-08-16
    https://doi.org/10.4084/mjhid.2016.037
    3087
    PDF: 934
    HTML: 1878
    Untitled: 150
    Untitled: 155
    Untitled: 149
    Untitled: 150
    Untitled: 141
  • INFECTIONS IN THALASSEMIA AND HEMOGLOBINOPATHIES

    Bianca Maria Ricerca, Arturo Di Girolamo, Deborah Rund
    e2009028
    2009-12-28
    1040
    PDF: 591
    HTML: 4264
  • VON WILLEBRAND FACTOR ABNORMALITIES STUDIED IN THE MOUSE MODEL: WHAT WE LEARNED ABOUT VWF FUNCTIONS

    Caterina Casari, Cecile V Denis
    e2013047
    2013-07-10
    https://doi.org/10.4084/mjhid.2013.047
    2108
    PDF: 933
    HTML: 9564
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Mediterranean Journal of Hematology and Infectious Diseases

is owned by the U.C.S.C. and it is published by PAGEPress®, Pavia, Italy. The MJHID is indexed and abstracted in Science Citation Index Expanded and Journal Citation Reports/InCites beginning with V. 7 (1) 2015.

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