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Editor-in-Chief: Giuseppe Leone | Italy

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  • REDUCTION OF INTRAMEDULLARY APOPTOSIS AFTER STEM CELL TRANSPLANTATION IN BLACK AFRICAN VARIANT OF PEDIATRIC SICKLE CELL ANEMIA.

    Antonella Isgrò, Pietro Sodani, Marco Marziali, Javid Gaziev, Daniela Fraboni, Katia Paciaroni, Cristiano Gallucci, Gioia De Angelis, Cecilia Alfieri, Michela Ribersani, Daniele Armiento, Andrea Roveda, Marco Andreani, Manuela Testi, Guido Lucarelli
    e2014054
    2014-07-06
    https://doi.org/10.4084/mjhid.2014.054
    2365
    PDF: 1073
    HTML: 2090
  • Multiple bone and joint disease in a sickle cell anaemia patient: a case report

    John Ayodele Olaniyi, Adekunle E Alagbe, Olutoogun O Toluwalase, Olorunsogo E Busari
    e2012023
    2012-05-03
    https://doi.org/10.4084/mjhid.2012.023
    1193
    PDF: 699
    HTML: 1694
  • HYDROXYCARBAMINE: FROM AN OLD DRUG USED IN MALIGNANT HEMOPATHIES TO A CURRENT STANDARD IN SICKLE CELL DISEASE

    Giovanna Cannas, Solene Poutrel, Xavier Thomas
    e2017015
    2017-02-15
    https://doi.org/10.4084/mjhid.2017.015
    3785
    PDF: 1123
    HTML: 1636
  • BACTERIAL INFECTIONS FOLLOWING SPLENECTOMY FOR MALIGNANT AND NONMALIGNANT HEMATOLOGIC DISEASES

    Giuseppe Leone, Eligio Pizzigallo
    e2015057
    2015-10-12
    https://doi.org/10.4084/mjhid.2015.057
    4630
    PDF: 1904
    HTML: 8269
  • SEROLOGICAL AND MOLECULAR DETECTION OF RICKETTSIA SPP STEMMING FROM HEMATOPHAGOUS VECTORS IN PATIENTS WITH MENINGEAL SYNDROME IN NORTHERN ALGERIA RICKETTSIA SPP IN PATIENTS WITH MENINGEAL SYNDROME

    HICHEM GHAOUI, IBRAHIM Nasir ADAM, BASHER Nosiba, TAKFARINAS IDRES, SORAYA TEMIM, ASMA SAAD-DJABALLAH , IDIR BITAM, NASSIMA ACHOUR
    e2025046
    2025-06-06
    https://doi.org/10.4084/MJHID.2025.046
    646
    PDF: 627
    HTML: 47
  • IRON DEFICIENCY ANAEMIA AMONG PRE-SCHOOL CHILDREN WITH SICKLE CELL ANAEMIA: STILL A RARE DIAGNOSIS?

    Olufemi Samuel Akodu, Omolara Adeolu Kehinde, Ijeoma Nnena Diaku-Akinwumi, Olisamedua Fidelis Njokanma
    e2013069
    2013-11-07
    https://doi.org/10.4084/mjhid.2013.069
    1264
    PDF: 791
    HTML: 2868
    cover leer: 129
  • FEASIBILITY AND EFFECTIVENESS OF TUBERCULOSIS ACTIVE CASE-FINDING AMONG CHILDREN LIVING WITH TUBERCULOSIS RELATIVES: A CROSS SECTIONAL STUDY IN GUINEA-BISSAU

    Raffaella Colombatti
    e2017059
    2017-10-15
    https://doi.org/10.4084/mjhid.2017.059
    2978
    PDF: 796
    HTML: 903
  • PREVALENCE AND FACTORS ASSOCIATED WITH HUMAN PARVOVIRUS B19 INFECTION IN SICKLE CELL PATIENTS HOSPITALIZED IN TANZANIA

    Florence Urio, Humphrey George, Furahini Tluway, Thomas B Nyambo, Bruno P Mmbando, Julie Makani
    e2019054
    2019-08-29
    https://doi.org/10.4084/mjhid.2019.054
    1589
    PDF: 1175
    HTML: 198
  • Clinical and laboratory features of Hemoglobin La Desirade variant in association with sickle cell and alpha thalassemia genes Clinical & laboratory features of Hb La Desirade trait and compound heterozygous for Hb La Desirade and HbS Hemoglobin.

    Salam Alkindi, Shoaib Al Zadjali, Mohamed Al Rawahi , Hamoud Al Haddabi, Shahina Daar, Refaat Abdullah Elsadek, Bahaa Eldeen Diab Sherkawy, Anil Pathare
    e2021010
    2021-01-01
    https://doi.org/10.4084/mjhid.2021.010
    1479
    PDF: 417
    HTML: 202
  • CHARACTERIZATION AND ANTIMICROBIAL SUSCEPTIBILITY PROFILE OF SEPTICAEMIA-CAUSING PATHOGENS ISOLATED FROM FEBRILE CHILDREN WITH SICKLE CELL DISEASE IN KANO, NIGERIA.

    Ibrahim Yusuf
    e2018016
    2018-02-15
    https://doi.org/10.4084/mjhid.2018.016
    2764
    PDF: 941
    HTML: 503
  • TUBERCULOSIS: MEDICO-LEGAL ASPECTS

    Giuseppe Vetrugno, Fabio De Giorgio, Francesco D'Alessandro
    e2014033
    2014-04-21
    https://doi.org/10.4084/mjhid.2014.033
    2376
    PDF: 1001
    HTML: 2834
  • ADVERSE PREGNANCY OUTCOMES IN SICKLE CELL TRAIT: A PROSPECTIVE COHORT STUDY EVALUATING CLINICAL AND HAEMATOLOGICAL PARAMETERS IN POSTPARTUM MOTHERS AND NEW-BORNS. Sickle cell trait pregnancy and outcomes

    r. Salam Al-Kindi
    e2023002
    2022-12-31
    https://doi.org/10.4084/MJHID.2023.002
    1220
    PDF: 1155
    HTML: 437
  • IS HEMOGLOBIN E GENE WIDELY SPREAD IN THE STATE OF MADHYA PRADESH IN CENTRAL INDIA? EVIDENCE FROM FIVE TYPICAL FAMILIES

    R S Balgir
    e2014060
    2014-09-01
    https://doi.org/10.4084/mjhid.2014.060
    1299
    PDF: 830
    HTML: 7899
    Untitled: 186
  • NEW THERAPEUTIC OPTIONS FOR THE TREATMENT OF SICKLE CELL DISEASE Guest Editor: Raffaella Origa

    Alessandro Matte, Filippo Mazzi, Enrica Federti, Oliviero Olivieri, Lucia De Franceschi
    e2019002
    2019-01-01
    https://doi.org/10.4084/mjhid.2019.002
    6632
    PDF: 3531
    HTML: 717
  • PREVENTION OF POST-TRANSFUSION HEPATITIS BY SCREENING OF ANTIBODY TO HEPATITIS B CORE ANTIGEN IN HEALTHY BLOOD DONORS

    Shamee Shastry, Sudha Bhat
    e2011062
    2011-12-17
    https://doi.org/10.4084/mjhid.2011.062
    1087
    PDF: 653
    HTML: 1227
    Title page: 173
  • Respiratory function in pediatric African SCA patients underwent bone marrow transplantation

    Antonella Isgrò, Javid Gaziev, Marco Marziali, Katia Paciaroni, Gioia De Angelis, Cecilia Alfieri, Michela Ribersani, Festus Olusola Olowoselu, Guido Lucarelli
    e2017030
    2017-04-15
    https://doi.org/10.4084/mjhid.2017.030
    2072
    PDF: 722
    HTML: 1015
    Spirometry in SCA patients before transplant: 178
    Spirometry in SCA patients post transplant: 161
  • DETECTION OF OCCULT GLOMERULAR DYSFUNCTION IN GLUCOSE SIX PHOSPHATE DEHYDROGENASE DEFICIENCY ANEMIA

    Gehan Abdel Hakeem, Emad Abdel Naem, Salwa Swelam, Laila Aboul Fotoh, Abdel Azeem Al Mazary, Ashraf Abdel Fadeil, Asmaa Abdel Hafez
    e2016038
    2016-08-20
    https://doi.org/10.4084/mjhid.2016.038
    3643
    PDF: 1187
    HTML: 1686
    Untitled: 139
  • DISSEMINATED HISTOPLASMOSIS AS AIDS PRESENTATION. CASE REPORT AND COMPREHENSIVE REVIEW OF CURRENT LITERATURE

    Paola Zanotti, Claudia Chirico, Maurizio Gulletta, Laura Ardighieri, Salvatore Casari, Eugenia Quiros Roldan, Ilaria Izzo, Gabriele Pinsi, Giovanni Lorenzin, Fabio Facchetti, Francesco Castelli, Emanuele Focà
    e2018040
    2018-07-01
    https://doi.org/10.4084/mjhid.2018.040
    3532
    PDF: 1245
    HTML: 696
    Figure 2: 416
    Figure 1: 3084
  • SCREENING OF HEPATITIS G AND EPSTEIN-BARR VIRUSES AMONG VOLUNTARY NON REMUNERATED BLOOD DONORS (VNRBD) IN BURKINA FASO, WEST AFRICA

    Issouf Tao, Cyrille Bisseye, Bolni Marius Nagalo, Mahamoudou Sanou, Alice Kiba, Guzin Surat, Tegwinde Rebecca Compaore, Lassina Traore, Albert Yonli, Jean-Baptiste Nikiema, Jean-Didier Zongo, Jacques Simpore
    e2013053
    2013-09-02
    https://doi.org/10.4084/mjhid.2013.053
    1442
    PDF: 728
    HTML: 2376
  • How we manage invasive fungal disease in acute myeloid leukemia patients with Glucose 6 Dehydrogenase deficiency

    Marco Sanna, Giovanni Caocci, Giorgio La Nasa
    e2017047
    2017-08-14
    https://doi.org/10.4084/mjhid.2017.047
    1769
    PDF: 874
    HTML: 930
    Referring article: 713
  • CURRENT KNOWLEDGE ON HIV-ASSOCIATED PLASMABLASTIC LYMPHOMA

    Michele Bibas, Jorge J Castillo
    e2014064
    2014-10-22
    https://doi.org/10.4084/mjhid.2014.064
    2495
    PDF: 1563
    HTML: 2333
    Table1: 172
  • Immune Biomarker Signature in the Diagnostic Workup of Fever Without Source: A Pilot Study

    Angela Maria Di Francesco, Giuliana Pasciuto, Laura Gerardino, Ludovico Luca Sicignano, Elena Verrecchia, Andrea Urbani, Donato Rigante, Raffaele Manna
    2026-02-28
    https://doi.org/10.4084/MJHID.2026.030
    391
    PDF: 227
    HTML: 82
  • HOMOZYGOUS DELETION ALFA-THALASSEMIA AND HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN, TWO GENETIC FACTORS PREDICTIVE THE REDUCTION OF MORBIDITY AND MORTALITY DURING PREGNANCY IN SICKLE CELL PATIENTS . A REPORT FROM DEMOCRATIC REPUBLIC OF CONGO ALPHA THALASSEMIA AND HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN REDUCE MORBIDITY DURING PREGNANCY IN SICKLE CELL PATIENTS

    Tite Minga MIKOBI, Prosper Tshilobo LUKUSA
    e2019039
    2019-06-24
    https://doi.org/10.4084/mjhid.2019.039
    9918
    PDF: 937
    HTML: 190
  • EVALUATION OF ORAL DOXYCYCLINE, AZITHROMYCIN, OR SEQUENTIAL DOXYCYCLINE-AZITHROMYCIN TREATMENT FOR SCRUB TYPHUS-

    Hanchen Liu, Weizhen Wang, Yuqing Dong
    2026-02-28
    https://doi.org/10.4084/MJHID.2026.020
    501
    PDF: 277
    HTML: 66
  • AGE AT DIAGNOSIS OF SICKLE CELL ANAEMIA IN LAGOS, NIGERIA

    Femi Akodu, I N Diaku-Akinwumi, O F Njokanma
    e2013001
    2013-01-02
    https://doi.org/10.4084/mjhid.2013.001
    1908
    PDF: 845
    HTML: 1839
  • THE PRICE OF MERCY: COMMENT TO THE PAPER "PREVENTION OF BETA-THALASSEMIA IN NORTHERN ISRAEL - A COST-BENEFIT ANALYSIS” BY KOREN ET AL

    Eliezer Rachmilewitz
    e2014022
    2014-03-10
    https://doi.org/10.4084/mjhid.2014.022
    1435
    PDF: 928
    HTML: 2075
  • EBV CHRONIC INFECTIONS

    Eligio Pizzigallo, Delia Racciatti, Valeria Gorgoretti
    e2010022
    2010-08-09
    https://doi.org/10.4084/mjhid.2010.022
    3328
    PDF: 1529
    HTML: 7767
  • CLASSIC KSHV/HHV-8-POSITIVE PRIMARY EFFUSION LYMPHOMA (PEL): A SYSTEMATIC REVIEW AND META-ANALYSIS OF CASE REPORTS

    Ilaria Cozzi, Giovanni Rossi, Emma Rullo, Valeria Ascoli
    e2022020
    2022-02-27
    https://doi.org/10.4084/MJHID.2022.020
    1457
    PDF: 898
    HTML: 280
  • DYNAMIC MONITORING OF ADAMTS 13 ACTIVITY FOR DIFFERENTIAL DIAGNOSIS ACROSS THE SPECTRUM OF SEPSIS ASSOCIATED WITH THROMBOTIC MICROANGIOPATIES Adamts 13 and Sepsis Associated with Thrombotic Thrombocytopenic Purpura

    Yi Liu, Fan Lu, Binbin Ji, Wei Song, Hui Shen, Yingjie Xu, bining Yang
    e2026019
    2026-02-28
    https://doi.org/10.4084/MJHID.2026.019
    510
    PDF: 313
    HTML: 71
  • A SEROPREVALENCE OF HBV, HCV AND HIV-1 AND CORRELATION WITH MOLECULAR MARKERS AMONG MULTI-TRANSFUSED THALASSEMIA PATIENTS IN WESTERN INDIA Incidence of serology & molecular of HIV, HBV and HCV in thalassemia patients

    Kanchan Mishra, Avani Shah, Krima Patel, Kanjaksha Ghosh, Sumit Bharadva
    e2020038
    2020-06-28
    https://doi.org/10.4084/mjhid.2020.038
    1235
    PDF: 737
    HTML: 463
  • Screening and genetic diagnosis of Hemoglobinopathies in Southern and Northern Europe: Two examples

    Antonio Amato, Piero C Giordano
    e2009007
    2009-08-07
    1111
    PDF: 463
    HTML: 1142
    Amato1: 152
    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: 228
    jdoe, : 236
    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: 140
  • SHORT TERM ADVANTAGES OF A PUBLIC-PRIVATE PARTNERSHIP FOR TUBERCULOSIS IN GUINEA BISSAU: REDUCTION OF MORTALITY AND INCREASED DIAGNOSTIC CAPACITY

    Fina Vieira, Mamadu Saliu Sanha, Fabio Riccardi, Raffaella Colombatti
    e2014049
    2014-06-29
    https://doi.org/10.4084/mjhid.2014.049
    1327
    PDF: 875
    HTML: 1270
    Untitled: 159
  • 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
    2216
    PDF: 1537
    HTML: 570
  • Postpandemic influenza A/H1N1pdm09 is still causing severe perinatal complications

    Hein Bogers, Dominique Bos, Sam Schoenmakers, Johannes J Duvekot
    e2015007
    2014-12-20
    https://doi.org/10.4084/mjhid.2015.007
    1294
    PDF: 954
    HTML: 1992
    Cover letter: 178
  • FOETAL HAEMOGLOBIN AND DISEASE SEVERITY IN NIGERIAN CHILDREN WITH SICKLE CELL ANAEMIA.

    Oluwagbemiga Adeodu, Morenike Akinlosotu, Samuel Adegoke, Saheed Oseni
    e2017063
    2017-11-01
    https://doi.org/10.4084/mjhid.2017.063
    5467
    PDF: 997
    HTML: 936
  • GENE THERAPY IN THALASSEMIA AND HEMOGLOBINOPATHIES

    Laura Breda, Roberto Gambari, Stefano Rivella
    e2009008
    2009-11-16
    1214
    PDF: 409
    HTML: 2865
  • CEREBRAL VENOUS THROMBOSIS IN THE MEDITERRANEAN AREA IN CHILDREN

    S Menascu, A Lotan, B Ben Zeev, U Nowak- Gottl, G Kenet
    e2011029
    2011-07-08
    https://doi.org/10.4084/mjhid.2011.029
    2457
    PDF: 918
    HTML: 2211
  • Hemophagocytic lymphohistiocytosis: an unusual complication in Orientia tsutsugamushi disease (scrub typhus).

    Aneesh Basheer, Somanath Padhi, Vinoth Boopathy, Saumyaranjan Mallick, Shashikala Nair, Renu G'Boy Varghese, Reba Kanungo
    e2015008
    2014-12-23
    https://doi.org/10.4084/mjhid.2015.008
    3935
    PDF: 1484
    HTML: 4316
  • PREVALENCE OF SERIOUS BACTERIAL INFECTIONS IN CHILDREN WITH SICKLE CELL DISEASE AT KING ABDULAZIZ HOSPITAL, AL AHSA Bacterial infections in children with sickle cell diseas

    Manal Alsaif, Joan Robinson, Moshtag Abdulbaqi, Mustafa Aghbari, Khalid Al Noaim, Muneera Alabdulqader
    e2021002
    2021-01-01
    https://doi.org/10.4084/mjhid.2021.002
    1396
    PDF: 529
    HTML: 195
  • ROLE OF CYTOKINES AS MOLECULAR MARKER OF DENGUE SEVERITY

    Priyanka Sehrawat, Ashutosh Biswas, Prabhat Kumar, Paras Singla, Naveet Wig, Lalit Dar, Rita Sood
    e2018023
    2018-04-20
    https://doi.org/10.4084/mjhid.2018.023
    3020
    PDF: 1107
    HTML: 363
  • PROCALCITONIN AS A BIOMARKER OF BACTERIAL INFECTION IN SICKLE CELL VASO-OCCLUSIVE CRISIS.

    Dilip Kumar Patel, Manoj Kumar Mohapatra, Ancil George Thomas, Siris Patel, Prasanta Purohit
    e2014018
    2014-02-16
    https://doi.org/10.4084/mjhid.2014.018
    2003
    PDF: 998
    HTML: 15639
    COVER LETTER: 163
  • ORAL IRON-HYDROXIDE POLYMALTOSE COMPLEX VERSUS SUCROSOMIAL IRON FOR CHILDREN WITH IRON DEFICIENCY WITH OR WITHOUT ANEMIA: A CLINICAL TRIAL WITH EMPHASIS ON INTESTINAL INFLAMMATION

    Miss Sonia Alexiadou, Mrs. Christina Tsigalou, Mrs. Eleni Kourkouni, Professor Aggelos Tsalkidis, Professor Elpis Mantadakis
    e2024075
    2024-10-31
    https://doi.org/10.4084/MJHID.2024.075
    1495
    PDF: 732
    HTML: 449
  • TUBERCULOSIS: EPIDEMIOLOGY AND CONTROL

    Giorgia Sulis, Alberto Roggi, Alberto Matteelli, Mario C. Raviglione
    e2014070
    2014-10-27
    https://doi.org/10.4084/mjhid.2014.070
    6683
    PDF: 3818
    HTML: 24838
  • THE HEMATOLOGICAL PARAMETERS AND BIOCHEMICAL MARKERS OF IRON STATUS IN ALFA-THALASSEMIA 3.7KB DELETION FROM METROPOLITAN REGION OF MANAUS, AMAZONAS, BRAZIL. alfa-Thalassemia 3.7 deletion From Amazonas, Brazil.

    Fernanda Cozendey Anselmo, Abdou Gafar Soumanou , Cleidiane de Aguiar Ferreira , Flora Maia Viga Sobrinha, Ana Caroline Santos Castro, Rafael Oliveira Brito, Adolfo José Mota, Marilda de Souza Gonçalves, Jose Pereira Moura Neto
    e2021001
    2021-01-01
    https://doi.org/10.4084/MJHID.2021.001
    4005
    PDF: 546
    HTML: 325
  • TUBERCULOSIS IN TROPICAL AREAS AND IMMIGRANTS

    Lorenzo Zammarchi, Filippo Bartalesi, Alessandro Bartoloni
    e2014043
    2014-05-31
    https://doi.org/10.4084/mjhid.2014.043
    3194
    PDF: 1261
    HTML: 6164
  • JUSTIFICATION OF UNIVERSAL IRON SUPPLEMENTATION FOR INFANTS 6-12 MONTHS IN REGIONS WITH A HIGH PREVALENCE OF THALASSEMIA Iron Supplementation for Infants 6-12 months in Regions with a High Prevalence of Thalassemia

    Phakatip Sinlapamongkolkul, Pacharapan Surapolchai, Vip Viprakasit
    e2023056
    2023-08-29
    https://doi.org/10.4084/MJHID.2023.056
    1921
    PDF: 570
    Suppl. Files: 263
    HTML: 149
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