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Editor-in-Chief: Giuseppe Leone | Italy

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  • Diagnostic Challenges of Hemoglobin (Hb) Hekinan with deletional a0-thalassemia and b0-thalassemia During Prenatal Screening for Fetal Hb E/β-Thalassemia Risk

    Dr. Piyatida Chumnumsiriwath, Prissana Charoenporn, Sawichayaporn Jermnim, Pawanrat Suannum, Monthira Samaisombat, Dr. Akamon Tapprom, Dr. Rawisut Deoisares, Dr. Peerapon Wong
    e2026064
    2026-09-01
    https://doi.org/10.4084/MJHID.2026.064
    115
    PDF: 96
    Html: 28
  • PATHOGENESIS OF MALARIA IN TISSUES AND BLOOD

    Beatrice Autino, Yolanda Corbett, Francesco Castelli, Donatella Taramelli
    e2012061
    2012-10-04
    https://doi.org/10.4084/mjhid.2012.061
    4773
    PDF: 2051
    HTML: 18213
  • REGULATORY T-CELLS IN CHRONIC LYMPHOCYTIC LEUKEMIA

    Giovanni D'arena, Giovanni Rossi, Barbara Vannata, Silvia Deaglio
    e2012053
    2012-08-09
    https://doi.org/10.4084/mjhid.2012.053
    2434
    PDF: 1071
    HTML: 7710
    Untitled: 329
    Fig2: 229
    Fig3: 224
    Fig4: 246
  • MANAGEMENT OF PORTAL VEIN THROMBOSIS IN CIRRHOTIC PATIENTS

    Lucio Amitrano, Maria Anna Guardascione
    e2009014
    https://doi.org/10.4084/mjhid.2009.014
    870
    PDF: 587
    HTML: 4041
  • 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
    3904
    PDF: 911
    HTML: 1614
  • DECREASED CD10 EXPRESSION IN THE BONE MARROW NEUTROPHILS OF HIV POSITIVE PATIENTS

    Annemarie Van de Vyver, Adele Visser
    e2010032
    2010-11-10
    https://doi.org/10.4084/mjhid.2010.032
    1411
    PDF: 950
    HTML: 1206
    Coverletter: 295
  • Formulas for the Detection ?-Thalassemia Carriers Are Affected by Changes in Red Cell Parameters

    Deniz Aslan
    e2018026
    2018-04-20
    https://doi.org/10.4084/mjhid.2018.026
    1446
    PDF: 730
    HTML: 416
  • HEMATOLOGY PATIENT PROTECTION DURING THE COVID-19 PANDEMIC IN ITALY: A NATIONWIDE NURSING SURVEY Hematology patient protection during the COVID-19

    Stefano Botti, Nicola Serra, Fausto Castagnetti, Sabina Chiaretti, Nicola Mordini, Gianpaolo Gargiulo, Laura Orlando
    e2021011
    2021-01-01
    https://doi.org/10.4084/mjhid.2021.011
    1836
    PDF: 671
    HTML: 304
  • INVASIVE FUNGAL INFECTIONS IN PATIENTS WITH CHRONIC LYMPHOPROLIFERATIVE DISORDERS IN THE ERA OF TARGET DRUGS

    Livio Pagano, Davide Facchinelli, Dr.
    e2018063
    2018-10-27
    https://doi.org/10.4084/mjhid.2018.063
    2188
    PDF: 1187
    HTML: 363
  • RECURRENT/PERSISTENT PNEUMONIA AMONG CHILDREN IN UPPER EGYPT

    Khaled Saad
    e2013028
    2013-04-18
    https://doi.org/10.4084/mjhid.2013.028
    2148
    PDF: 969
    HTML: 252
    Untitled: 281
    Untitled: 276
    cover letter: 223
  • COEXISTENCE OF MULTIPLE GENE VARIANTS IN SOME PATIENTS WITH ERYTHROCYTOSES Multiple gene variants in erythrocytosis

    Andrea Benetti, Irene Bertozzi, PhD, MD, Giulio Ceolotto, Irene Cortella, Daniela Regazzo, Giacomo Biagetti, Elisabetta Cosi, Maria Luigia Randi, MD, Prof
    e2024021
    2024-02-29
    https://doi.org/10.4084/MJHID.2024.021
    964
    PDF: 1312
    HTML: 161
  • STUDY OF SERUM HAPTOGLOBIN LEVEL AND ITS RELATION TO ERYTHROPOIETIC ACTIVITY IN BETA THALASSEMIA CHILDREN .

    Seham Ragab, Manal A. Safan, Eman A. Badr
    e2015019
    2015-02-12
    https://doi.org/10.4084/mjhid.2015.019
    2497
    PDF: 1241
    HTML: 2624
    Study of serum haptoglobin level in thalassemia: 436
    Figures: 262
  • WALDENSTRÖM MACROGLOBULINEMIA - A STATE-OF-THE-ART REVIEW: PART 1: EPIDEMIOLOGY, PATHOGENESIS, CLINICOPATHOLOGIC CHARACTERISTICS, DIFFERENTIAL DIAGNOSIS, RISK STRATIFICATION, AND CLINICAL PROBLEMS

    Michele Bibas, Shayna Sarosiek, Jorge J. Castillo
    e2024061
    2024-06-29
    https://doi.org/10.4084/MJHID.2024.061
    3138
    PDF: 3393
    HTML: 789
  • Parvovirus B19-triggered acute hemolytic anemia and thrombocytopenia in a child with Evans syndrome

    ELPIS MANTADAKIS
    e2018018
    2018-03-01
    https://doi.org/10.4084/mjhid.2018.018
    3720
    PDF: 1057
    HTML: 484
    Table 1.: 283
  • CONCISE REVIEW ON THE FREQUENCY, MAJOR RISK FACTORS AND SURVEILLANCE OF HEPATOCELLULAR CARCINOMA (HCC) IN ?-THALASSEMIAS: PAST, PRESENT AND FUTURE PERSPECTIVES Thalassaemia transfusion dependent, Hepatitis C, hepatocarcinoma.

    Vincenzo De Sanctis
    e2020006
    2020-01-01
    https://doi.org/10.4084/mjhid.2020.006
    4444
    PDF: 1610
    HTML: 481
  • 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
    904
    PDF: 616
    HTML: 189
  • A CASE OF CONGENITAL DYSERYTHROPOIETIC ANEMIA MASKED BY HEMOGLOBIN H DISEASE

    Xiaolin Yin
    e2024059
    2024-06-29
    https://doi.org/10.4084/MJHID.2024.059
    822
    PDF: 922
    HTML: 129
  • Can Polycythemia Vera evolve from Acute Myeloid Leukemia? A Case Report Showing a Simultaneous Minor JAK2 V617F Mutated Clone, De novo polycythemia vera following AML remission

    Beatrice Borsellino, Arianna Savi, Maria Rosaria Pascale, Elisa Meddi, Antonio Cristiano, TIZIANA OTTONE, Maria Cristina Rapanotti, Mariadomenica Divona, SERENA TRAVAGLINI, Enrico Attardi, Elisa Buzzatti, Francesco Buccisano, Maria Teresa Voso
    e2022058
    2022-06-29
    https://doi.org/10.4084/MJHID.2022.058
    1853
    PDF: 863
    HTML: 311
  • PATHOGENESIS AND TREATMENT OF THROMBOHEMORRHAGIC DIATHESIS IN ACUTE PROMYELOCYTIC LEUKEMIA

    Anna Falanga, Laura Russo, Carmen J Tartari
    e2011068
    2011-12-21
    https://doi.org/10.4084/mjhid.2011.068
    1994
    PDF: 893
    HTML: 10368
    Figures 1,2,3: 279
  • 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
    2295
    PDF: 1032
    HTML: 9690
  • CUPROPTOSIS: A REVIEW ON MECHANISMS, ROLE IN SOLID AND HEMATOLOGICAL TUMORS, AND ASSOCIATION WITH VIRAL INFECTIONS

    MAURIZIO MARTINI, Pietro Tralongo, Mariagiovanna Ballato, Vincenzo Fiorentino, Walter Giordano, Valeria zuccalà, Cristina Pizzimenti, Arianna Bakacs, Antonio Ieni, Giovanni Tuccari, Guido Fadda, Luigi Maria Larocca
    e2025052
    2025-06-29
    https://doi.org/10.4084/MJHID.2025.052
    2011
    PDF: 1127
    HTML: 971
  • 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
    2190
    PDF: 1138
    HTML: 981
    Figure 1: 216
    Figure 2: 238
  • Graves’ disease thyrotoxicosis and propylthiouracil related agranulocytosis successfully treated with therapeutic plasma exchange and g-csf followed by total thyroidectomy.

    Anna Candoni
    e2017058
    2017-10-16
    https://doi.org/10.4084/mjhid.2017.058
    3100
    PDF: 950
    HTML: 1447
    Fig.1: 219
    Fig.2: 221
  • SICKLE CELL DISEASE AND VENOUS THROMBOEMBOLISM

    Zohreh Rahimi, Abbas Parsian
    e2011024
    2011-05-23
    https://doi.org/10.4084/mjhid.2011.024
    2414
    PDF: 1009
    HTML: 2411
  • MOLECULAR ANALYSIS OF NON-TRANSFUSION DEPENDENT THALASSEMIA ASSOCIATED WITH HEMOGLOBIN E-?-THALASSEMIA DISEASE WITHOUT ?--THALASSEMIA

    Paramee Phanrahan, Supawadee Yamsri, Nattiya Teawtrakul, Goonnapa Fucharoen, Kanokwan Sanchaisuriya, Supan Fucharoen
    e2019038
    2019-06-24
    https://doi.org/10.4084/mjhid.2019.038
    1620
    PDF: 1126
    HTML: 267
  • WALDENSTROM’S MACROGLOBULINEMIA: AN UPDATE

    Maddalena Mazzucchelli, Anna Maria Frustaci, Marina Deodato, Roberto Cairoli, Alessandra Tedeschi
    e2018004
    2018-01-01
    https://doi.org/10.4084/mjhid.2018.004
    7955
    PDF: 2524
    HTML: 2161
    Table 1.: 277
    Table 2.: 288
    Table 3.: 267
    Table 4.: 263
  • CONTRIBUTION OF MARITAL DISTANCE TO COMMUNITY INBREEDING, HOMOZYGOSIS, AND REPRODUCTIVE WASTAGE FOR RECESSIVELY INHERITED GENETIC DISORDERS IN MADHYA PRADESH, INDIA

    R S Balgir
    e2013063
    2013-11-04
    https://doi.org/10.4084/mjhid.2013.063
    1364
    PDF: 1054
    HTML: 1434
    Untitled: 134
  • ON THE VERSATILITY OF VON WILLEBRAND FACTOR

    Antoine Rauch, Peter Lenting
    e2013046
    2013-07-10
    https://doi.org/10.4084/mjhid.2013.046
    2984
    PDF: 1234
    HTML: 11433
  • TP53-MUTATED MYELODYSPLASIA AND ACUTE MYELOID LEUKEMIA TP53 in MDS and AML

    Ugo Testa, Dr. Germana Castelli, Dr. Elvira Pelosi
    e2023038
    2023-06-29
    https://doi.org/10.4084/MJHID.2023.038
    2450
    PDF: 1903
    HTML: 1064
  • LYMPHOPROLIFERATIVE SYNDROMES ASSOCIATED WITH HUMAN HERPESVIRUS-6A AND HUMAN HERPESVIRUS-6B

    Eva Eliassen, Gerhard R Krueger, Mario Luppi, Dharam Ablashi
    e2018035
    2018-05-01
    https://doi.org/10.4084/mjhid.2018.035
    3927
    PDF: 1700
    HTML: 879
    Figures . Eliassian: 301
  • The diagnostic approach to central adrenocortical insufficiency (CAI) in thalassemia

    Vincenzo De Sanctis, Heba Elsedfy, Ashraf T Soliman
    e2016026
    2016-05-01
    https://doi.org/10.4084/mjhid.2016.026
    3224
    PDF: 1062
    HTML: 2819
  • Screening and genetic diagnosis of Hemoglobinopathies in Southern and Northern Europe: Two examples

    Antonio Amato, Piero C Giordano
    e2009007
    2009-08-07
    1302
    PDF: 534
    HTML: 1218
    Amato1: 224
    Figure 2 A: Prospective (grey columns) versus retrospective prevention (black columns) among indigenous couples at risk (left) and immigrant couples (right). Among immigrant couples the prevention it is still largely retrospective, while for Italian coupl: 300
    jdoe, : 306
    Figure 2 b: Prospective (grey columns) versus retrospective prevention (black columns) among indigenous couples at risk (left) and immigrant couples (right). Among immigrant couples the prevention it is still largely retrospective, while for Italian coupl: 199
  • USE OF HEMATOPOIETIC GROWTH FACTOR IN THE MANAGEMENT OF HEMATOLOGICAL SIDE EFFECTS ASSOCIATED TO ANTIVIRAL TREATMENT FOR HCV HEPATITIS

    Paola Mancino, Katia Falasca, Claudio Ucciferri, Eligio Pizzigallo, Jacopo Vecchiet
    e2010003
    2010-03-26
    https://doi.org/10.4084/mjhid.2010.003
    1317
    PDF: 589
    HTML: 970
  • Anemia in the elderly: not always what it seems.

    Marco Cerrano, Elena Crisà, Valentina Giai, Mario Boccadoro, Dario Ferrero
    e2016017
    2016-02-25
    https://doi.org/10.4084/mjhid.2016.017
    3432
    PDF: 1153
    HTML: 1812
    Figure 1: 246
    Figure 1 revised: 261
  • 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
    1224
    PDF: 588
    HTML: 398
  • BONE MARROW ABONRMALITIES IN HIV INFECTION

    Sharad Antiram Dhurve
    e2013033
    2013-06-03
    https://doi.org/10.4084/mjhid.2013.033
    2022
    PDF: 1209
    HTML: 1787
  • SYSTEMIC MASTOCYTOSIS: MOLECULAR LANDSCAPE AND IMPLICATIONS FOR TREATMENT

    Cecilia Monaldi, Sara De Santis, Manuela Mancini, Samantha Bruno, Michele Cavo, Simona Soverini
    e2021046
    2021-06-28
    https://doi.org/10.4084/MJHID.2021.046
    1547
    PDF: 808
    HTML: 478
  • PREVALENCE OF HEPATITIS B, HEPATITIS C AND HIV IN MULTIPLY TRANSFUSED SICKLE CELL DISEASE PATIENTS FROM OMAN HBV,HCV and HIV and Sickle Cell Disease.

    Anil Pathare, Salam Alkindi, prof.
    e2019058
    2019-10-30
    https://doi.org/10.4084/mjhid.2019.058
    1773
    PDF: 1093
    HTML: 561
  • LIVER IRON CONTENT IN INDIVIDUALS WITH LIVER IRON CONTENT IN INDIVIDUALS WITH Β-THALASSEMIA TRAIT AND HYPERFERRITINEMIA: ROLE OF METABOLIC ALTERATIONS, HFE GENOTYPES, AND CIRRHOSIS.: ROLE OF METABOLIC ALTERATIONS, HFE GENOTYPES, AND CIRRHOSIS. Β-THALASSEMIA TRAIT AND HYPERFERRITINEMIA

    Alberto Piperno
    e2026051
    2026-06-30
    https://doi.org/10.4084/MJHID.2026.051
    316
    PDF: 343
    Suppl. Files: 47
    HTML: 156
  • THE HISTORY OF DEFERIPRONE (L1) AND THE COMPLETE TREATMENT OF IRON OVERLOAD IN THALASSAEMIA The history and roles of deferiprone

    George J Kontoghiorghes, Marios Kleanthous, Christina N. Kontoghiorghe
    e2020011
    2020-01-01
    https://doi.org/10.4084/mjhid.2020.011
    2715
    PDF: 1678
    HTML: 729
  • PLATELET COUNT RESPONSE TO HELICOBACTER PYLORI ERADICATION IN IRANIAN ?PATIENTS WITH IDIOPATHIC THROMBOCYTOPENIC ?PURPURA

    Mohammad Erfan Zare
    e2012056
    2012-08-10
    https://doi.org/10.4084/mjhid.2012.056
    2063
    PDF: 886
    HTML: 1517
  • MPN/MDS OVERLAP SYNDROME ANTICIPATED BY A SEVERE BLEEDING DIATHESIS: HYPOTHESIS OF A PRE-EXISTING PLATELET DISORDER

    Paola Ranalli, Stefano Baldoni, Daniela Bruno, Mauro Di Ianni
    e2024067
    2024-08-31
    https://doi.org/10.4084/MJHID.2024.067
    1297
    PDF: 716
    Html: 196
  • EVALUATION OF GLUTATHIONE-S-TRANSFERASE P1 POLYMORPHISM AND ITS RELATION TO BONE MINERAL DENSITY IN EGYPTIAN CHILDREN AND ADOLESCENTS WITH BETA- THALASSEMIA MAJOR

    Seham Ragab
    e2016004
    2016-01-01
    https://doi.org/10.4084/mjhid.2016.004
    4008
    PDF: 926
    HTML: 2481
    Figures: 224
  • 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
    3060
    PDF: 1526
    HTML: 332
  • T-cell Large Granular Lymphocytic Leukemia Manifesting in Patients with HIV-1 Infection: Cases Series and Review of the Literature

    Ashley M Rose, Leidy Isenalumhe, Magali VanDenBergh, Lubomir Sokol
    e2018036
    2018-06-21
    https://doi.org/10.4084/mjhid.2018.036
    2722
    PDF: 1006
    HTML: 425
  • AN OBSERVATIONAL STUDY OF THE EFFECT OF HEMOGLOBINOPATHY, ALPHA THALASSEMIA AND HEMOGLOBIN E ON P. VIVAX PARASITEMIA

    Suparak Para, Puncharee Mungkalasut, Makamas Chanda, Issarang Nuchprayoon, Srivicha Krundsood, Chalisa Louicharoen Cheepsunthorn
    e2018015
    2018-02-16
    https://doi.org/10.4084/mjhid.2018.015
    3999
    PDF: 978
    HTML: 479
    Distribution of malaria patient cohort along Thailand and borders during 2011-2012: 254
  • DIAMOND BLACKFAN ANEMIA: A TERTIARY CARE CENTRE EXPERIENCE

    avinash kumar singh, tulika seth, nita radhakrishnan, pravas mishra, manoranjan mahapatra, haraprasad pati
    e2013039
    2013-06-03
    https://doi.org/10.4084/mjhid.2013.039
    2772
    PDF: 911
    HTML: 3612
    Diamond Blackfan Anemia: A Tertiary care centre experience: 378
  • TREATMENT OF ACUTE PROMYELOCYTIC LEUKEMIA WITH SINGLE-AGENT ARSENIC TRIOXIDE

    Vikram Mathews, Ezhilarasi Chendamarai, Biju George, Auro Viswabandya, Alok Srivastava
    e2011056
    2011-11-28
    https://doi.org/10.4084/mjhid.2011.056
    3819
    PDF: 1031
    HTML: 4633
  • Microangiopathic Hemolytic Anemia in 57-year-old woman with Borderline Serous Tumor of the Ovary:Real-Time Management of Common Pathways of Hemostatic Failure

    Gloria Joan Morris
    e2012030
    2012-05-06
    https://doi.org/10.4084/mjhid.2012.030
    1327
    PDF: 892
    HTML: 12961
  • PREDISPOSING FACTORS TO INFECTIONS IN THALASSEMIA SYNDROME PATIENTS

    Eman M Mansory, Lina M. Abdulrahman, Balsam Osman, Sawsan M. Sawsan, Assil F. Ruckn, Marwa Aljedaani, Nemmat Hassan, Ahmed S. Barefah, Hatem M. Alahwal, Yassir Daghistani, Salem M. Bahashwan, Abdullah T. Almohammadi, Osman O. Radhwi
    e2025055
    2025-08-31
    https://doi.org/10.4084/MJHID.2025.055
    1951
    PDF: 1623
    HTML: 511
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