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Editor-in-Chief: Giuseppe Leone | Italy

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  • VITAMIN D STATUS IN THALASSEMIA MAJOR: AN UPDATE

    Ashraf Tawfik Soliman
    e2013057
    2013-09-02
    https://doi.org/10.4084/mjhid.2013.057
    2631
    PDF: 1054
    HTML: 2552
  • ASSOCIATION OF VDBP RS4701 VARIANT, BUT NOT VDR/RXR-? OVER-EXPRESSION WITH BONE MINERAL DENSITY IN PEDIATRIC ?-THALASSEMIA PATIENTS Vitamin D metabolic axis and BMD in ?-thalassemia

    Shaimaa Sahmoud, Mostafa S. Ibrahim, Eman A. Toraih, Noha Kamel, Manal Fawzy, Samar Elfiky
    e2020037
    2020-06-28
    https://doi.org/10.4084/mjhid.2020.037
    1172
    PDF: 703
    HTML: 175
  • BONE MINERAL DENSITY AND VITAMIN D RECEPTOR GENETIC VARIANTS IN EGYPTIAN CHILDREN WITH BETA THALASSEMIA ON VITAMIN D SUPPLEMENTATION

    Hadeer A Abbassy, Reham Abdel Haleem Abo Elwafa, Omneya Magdy Omar
    e2019013
    2019-01-01
    https://doi.org/10.4084/mjhid.2019.013
    2216
    PDF: 1204
    HTML: 202
  • NEGATIVE IMPACT OF PROLONGED ANTIBIOTICS OR PERSISTENT DIARRHEA ON VITAMIN K1 LEVELS IN 2-24 WEEKS AGED EGYPTIAN INFANTS

    Mohsen Elalfy, Fatma S E Ebeid, Iman Elagouza, Fatma Ibrahim, Noura Hassan, Beshoy Botros
    e2018010
    2018-01-01
    https://doi.org/10.4084/mjhid.2018.010
    4225
    PDF: 819
    HTML: 959
  • The INFLUENCE OF NUTRITION ON DISEASE SEVERITY AND HEALTH-RELATED QUALITY OF LIFE IN ADULTS WITH SICKLE CELL DISEASE A Prospective Longitudinal Study

    Sanaa Kamal, Moheyeldeen Mohamed Naghib, Jamaan Al Zahrani, Huda Hassan, Karim Abdel Aziz Moawado, Omar Arrahman
    e2021007
    2021-01-01
    https://doi.org/10.4084/mjhid.2021.007
    2243
    PDF: 908
    HTML: 292
  • HEMOGLOBIN H DISEASE AND GROWTH: A COMPARATIVE STUDY OF DHbH AND NDHbH PATIENTS

    Issanun Hunnuan, Kleebsabai SAnpakit, Ornsuda Lertbannaphong, Jassada Buaboonnam
    e2023045
    2023-08-29
    https://doi.org/10.4084/MJHID.2023.045
    1190
    PDF: 632
    HTML: 152
  • CUTANEOUS HYPERPIGMENTATION IN MEGALOBLASTIC ANEMIA: A FIVE YEAR RETROSPECTIVE REVIEW.

    Somanath Padhi, RajLaxmi Sarangi, Anita Ramdas, Kandasamy Ravichandran, Renu G’Boy Varghese, Thomas Alexander, George Kurien, Sudhagar Mookkappan
    e2016021
    2016-04-10
    https://doi.org/10.4084/mjhid.2016.021
    4461
    PDF: 987
    HTML: 12687
  • HOW THE HEMOSTASIS LABORATORY CAN HELP CLINICIANS TO MANAGE PATIENTS ON ORAL ANTICOAGULANTS

    Armando Tripodi
    e2024027
    2024-02-29
    https://doi.org/10.4084/MJHID.2024.027
    972
    PDF: 1318
    HTML: 113
  • 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
    4174
    PDF: 1497
    HTML: 436
  • Hypophosphatemic osteomalacia associated with tenofovir: a multidisciplinary approach is required.

    Giuseppe Vittorio De Socio, Gianluigi Fabbriciani, Marco Massarotti, Salvatore Messina, Enisia Cecchini, Bianca Marasini
    e2012025
    2012-05-04
    https://doi.org/10.4084/mjhid.2012.025
    1312
    PDF: 816
    HTML: 10025
    cover letter to the editor: 154
    tile page: 239
  • DISTRIBUTION OF DNA DAMAGE REPAIR GENE POLYMORPHISM hOGG1, XRCC1 and p53 AMONG SICKLE CELL DISEASE PATIENTS IN INDIA

    Sudhansu Sekhar Nishank
    e2015046
    2015-07-02
    https://doi.org/10.4084/mjhid.2015.046
    1489
    PDF: 766
    HTML: 1466
    Table Genotype and allele frequencies of hOGG1 codon 326 Ser>Cys and p53 72Arg>Pro polymorphisms among SCD patients and control group: 168
  • Severe acute axonal neuropathy following treatment with arsenic trioxide for acute promyelocytic leukemia: a case report

    Marcus Kuhn, Mithia Nabergoj, Kety Sammartin, Fabrizio Vianello
    e2016023
    2016-05-01
    https://doi.org/10.4084/mjhid.2016.023
    3861
    PDF: 975
    HTML: 1476
  • 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
    2852
    PDF: 853
    HTML: 1401
    Fig.1: 153
    Fig.2: 160
  • ACQUIRED REFRACTORY IRON DEFICIENCY

    Margherita Migone De Amicis, Alessandro Rimondi, Luca Elli, Irene Motta
    e2021028
    2021-04-29
    https://doi.org/10.4084/MJHID.2021.028
    2770
    PDF: 1025
    HTML: 741
  • EXTREMELY OLD PATIENTS HOSPITALIZED IN INTERNAL MEDICINE: WHAT ABOUT THEIR ANEMIA? Anemia in the elderly

    . Maria Luigia Randi, Prof. Fabrizio Fabris
    Page e2021038
    2021-04-29
    https://doi.org/10.4084/MJHID.2021.038
    1497
    PDF: 486
    HTML: 216
  • 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
    3874
    PDF: 824
    HTML: 2419
    Figures: 159
  • CLINICAL CARE PATHWAY AND MANAGEMENT OF MAJOR BLEEDING ASSOCIATED WITH NON-VITAMIN K ANTAGONIST ORAL ANTICOAGULANTS: A MODIFIED DELPHI CONSENSUS FROM SAUDI ARABIA AND UAE

    Abdulrahman Al Raizah, Fakhr Alayoubi, Galal Hassan Abdelnaby, Hazzaa Alzahrani, Majid Farraj Bakheet, Mohammed A Alskaini, Rasha Buhumaid, Sameer Al Awadhi, Sara Nooruddin Kazim, Thiagarajan Jaiganesh, Zohair Al Asiri
    e2024038
    2024-04-30
    https://doi.org/10.4084/MJHID.2024.038
    2543
    PDF: 1151
    HTML: 98
  • IRON DEFICIENCY ANEMIA IN CHILDREN RESIDING IN HIGH AND LOW-INCOME COUNTRIES: RISK FACTORS, PREVENTION, DIAGNOSIS AND THERAPY

    ELPIS MANTADAKIS
    e2020041
    2020-06-28
    https://doi.org/10.4084/mjhid.2020.041
    9366
    PDF: 6112
    HTML: 582
  • Acquired Sideroblastic Anemia: An exploratory Comparative Statistical Analysis Between Clonal and Non-clonal cases Acquired Sideroblastic Anemia

    Dina Sameh Soliman, Samah Kohla, Shehab Fareed, Susanna Akiki , Aliaa Amer, Ibrahim Ganwo, Prem Chandra, Halima El-Omri, Feryal Ibrahim
    e2022067
    2022-08-27
    https://doi.org/10.4084/MJHID.2022.067
    903
    PDF: 558
    HTML: 321
  • INSULIN-LIKE GROWTH FACTOR-1 (IGF-1): DEMOGRAPHIC, CLINICAL AND LABORATORY DATA IN 120 CONSECUTIVE ADULT PATIENTS WITH THALASSAEMIA MAJOR

    V. De Sanctis
    e2014.074
    2014-11-01
    https://doi.org/10.4084/mjhid.2014.074
    2211
    PDF: 920
    HTML: 26924
  • JADENU® SUBSTITUTING EXJADE® IN IRON OVERLOADED ?- THALASSEMIA MAJOR (BTM) PATIENTS: A PRELIMINARY REPORT OF THE EFFECTS ON THE TOLERABILITY, SERUM FERRITIN LEVEL, LIVER IRON CONCENTRATION AND BIOCHEMICAL PROFILES

    Vincenzo De Sanctis
    e2018064
    2018-10-27
    https://doi.org/10.4084/mjhid.2018.064
    2553
    PDF: 1192
    HTML: 236
  • REAL WORLD DATA ON CHARACTERISTICS AND MANAGEMENT OF COMMUNITY PATIENTS RECEIVING ANTICOAGULATION THERAPY WHO PRESENTED WITH ACUTE BLEEDING TO THE EMERGENCY DEPARTMENT AT A REGIONAL AUSTRALIAN HOSPITAL: A PROSPECTIVE OBSERVATIONAL STUDY. Anticoagulation and bleeding ?

    Fayez Hanna, Annemarie Hyppa, Ajay Prakash, Usira Vithanarachchi, Hizb U Dawar, Zar Sanga, George Olabode, Hamish Crisp, Professor Alhossain A. Khalafallah
    e2021017
    2021-02-26
    https://doi.org/10.4084/mjhid.2021.017
    1530
    PDF: 513
    HTML: 299
  • 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
    1284
    PDF: 807
    HTML: 2889
    cover leer: 136
  • CARDIAC FUNCTION AND IRON CHELATION IN THALASSEMIA MAJOR AND INTERMEDIA: A REVIEW OF THE UNDERLYING PATHOPHYSIOLOGY AND APPROACH TO CHELATION MANAGEMENT

    Athanasios Aessopos, Vasilios Berdoukas
    e2009002
    2009-07-18
    1550
    PDF: 470
    HTML: 1424
  • ULTRASOUND AS FIRST LINE STEP IN ANAEMIA DIAGNOSTICS

    chiara mozzini, giancarlo pesce, alder casadei, domenico girelli, maurizio soresi
    e2019066
    2019-10-30
    https://doi.org/10.4084/mjhid.2019.066
    1342
    PDF: 863
    HTML: 1774
  • Tuberculosis after gastrectomy, plasmatic concentration of antitubercular drugs

    Giuseppe Vittorio De Socio, Antonio D'Avolio, Alessio Sgrelli, Lorena Baietto, Lisa Malincarne, Giovanni Di Perri, Franco Baldelli
    e2012007
    2012-01-23
    https://doi.org/10.4084/mjhid.2012.007
    1556
    PDF: 762
    HTML: 800
    tile page: 148
    Table 1: 152
  • EBV CHRONIC INFECTIONS

    Eligio Pizzigallo, Delia Racciatti, Valeria Gorgoretti
    e2010022
    2010-08-09
    https://doi.org/10.4084/mjhid.2010.022
    3405
    PDF: 1546
    HTML: 7784
  • BISPHOSPHONATES IN LANGERHANS CELL HISTIOCYTOSIS: AN INTERNATIONAL RETROSPECTIVE CASE SERIES

    Deepak Chellapandian, Polyzois Makras, Gregory Kaltsas, Cor van den Bos, Lamia Naccache, Raajit Rampal, Anne-Sophie Carret, Sheila Weitzman, R. Maarten Egeler, Oussama Abla
    e2016033
    2016-07-01
    https://doi.org/10.4084/mjhid.2016.033
    3634
    PDF: 1208
    HTML: 1044
  • An unusual cause of anemia and encephalopathy

    Sanjeev Kumar Sharma, Dharma Choudhary, Anil Handoo, Gaurav Dhamija, Gaurav Kharya, Vipin Khandelwal, Mayank Dhamija, Sweta Kothari
    e2015036
    2015-04-24
    https://doi.org/10.4084/mjhid.2015.036
    3791
    PDF: 839
    HTML: 1499
  • COBALAMIN DEFICIENCY IN THE ELDERLY

    Giacomo Marchi, Fabiana Busti, Acaynne Lira Zidanes, Alice Vianello, Domenico Girelli
    e2020043
    2020-06-28
    https://doi.org/10.4084/mjhid.2020.043
    2426
    PDF: 1889
    HTML: 474
  • HEAVY-CHAIN DISEASES AND MYELOMA-ASSOCIATED FANCONI SYNDROME: AN UPDATE

    Roberto Ria, Franco Dammacco, Angelo Vacca
    e2018011
    2018-01-01
    https://doi.org/10.4084/mjhid.2018.011
    5071
    PDF: 1594
    HTML: 1345
  • GROUP-BASED TRAJECTORY MODELING OF PLATELET IN PATIENTS WITH APLASTIC ANEMIA: A STUDY BASED ON THE MIMIC DATABASE

    Lang Peng, Lixin Zou, Xiaoliu Liu
    e2025012
    2025-02-27
    https://doi.org/10.4084/MJHID.2025.012
    958
    PDF: 967
    Suppl. Files: 620
    HTML: 105
  • A novel ALAS2 mutation causes congenital sideroblastic anemia

    Kun Yang
    e2023062
    2023-10-30
    https://doi.org/10.4084/MJHID.2023.062
    645
    PDF: 503
    HTML: 140
  • CLINICAL ASPECTS OF UNCOMPLICATED AND SEVERE MALARIA

    Alessandro Bartoloni, Lorenzo Zammarchi
    e2012026
    2012-05-04
    https://doi.org/10.4084/mjhid.2012.026
    7774
    PDF: 4044
    HTML: 7313
  • 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
    3267
    PDF: 998
    HTML: 1758
    Figure 1: 164
    Figure 1 revised: 167
  • A PROSPECTIVE, OBSERVATIONAL STUDY OF ADVERSE REACTIONS TO DRUG REGIME FOR MULTI-DRUG RESISTANT PULMONARY TUBERCULOSIS IN CENTRAL INDIA.

    Dr. Rohan C. Hire, Dr. A. S. Kale, Dr. G. N. Dakhale, Dr. Nilesh N. Gaikwad
    e2014061
    2014-09-01
    https://doi.org/10.4084/mjhid.2014.061
    1750
    PDF: 1046
    HTML: 3802
  • ANORECTAL PATHOLOGIES IN THE COURSE OF ACUTE LEUKAEMIAS: PREDICTIVE PARAMETERS Anorectal pathologies in leukemias

    Fatma Yılmaz, Bugra Saglam, Ufuk Gorduk, Ugur Kalan, Hacer Berna Afacan Öztürk, Ahmet Kursad Gunes, Murat Albayrak
    e2024071
    2024-08-31
    https://doi.org/10.4084/MJHID.2024.071
    1143
    PDF: 698
    Html: 85
  • Breastfeeding in patients with chronic myeloid leukaemia: case series with measurements of drug concentrations in maternal milk and review of literature

    Ekaterina Chelysheva, Sergey Aleshin, Evgenia Polushkina, Roman Shmakov, Igor Shokhin, Ghermes Chilov, Anna Turkina
    e2018027
    2018-05-01
    https://doi.org/10.4084/mjhid.2018.027
    3078
    PDF: 965
    HTML: 339
  • 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
    4392
    PDF: 1891
    HTML: 17715
  • ASSESSMENT OF CONGENITAL NEUTROPENIA IN CHILDREN: COMMON CLINICAL SCENERIES AND CLUES FOR MANAGEMENT Assessment of congenital neutropenia in children

    Ilaria Lazzareschi, Elena Rossi, Antonietta Curatola, Giovanna Capozio, Luca Benacquista, Ludovica Iezzi, Donato Rigante
    e2022008
    2022-01-01
    https://doi.org/10.4084/MJHID.2022.008
    1922
    PDF: 1077
    HTML: 593
  • THALASSAEMIA AND ABERRATIONS OF GROWTH AND PUBERTY

    Andreas Kyriakou, Nicos Skordis
    e2009003
    2009-07-28
    1093
    PDF: 453
    HTML: 3205
  • AGING WITH THALASSEMIA AND SICKLE CELL DISEASE: A GERONTOLOGICAL MODEL OF ACCELERATED MULTIMORBIDITY AND FUNCTION-CENTERED CARE BEYOND MIDLIFE Thalassemia and Sickle Cell Diseases: Effect of Aging

    Dr.Sophia Delicou, Dr.Ioannis Ilias, Dr.Athanasia Kapota, Dr.Elena Papatheodorou, Dr.Maria Moraki, Dr.Aikaterini Xydaki, Dr.Alexandra Mika, Dr.Panagiota Giannou, Dr.Irene Kouroukli, Dr.Theodoros Aforozis, Dr.Myrto Palkopoulou, Dr.Christos Savvidis, Dr.Iliana Mani, Prof.Constantina Aggeli, Prof. John Koskinas
    e2026039
    2026-04-30
    https://doi.org/10.4084/MJHID.2026.039
    177
    PDF: 125
    Suppl. Files: 26
    HTML: 5
  • 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
    2321
    PDF: 1559
    HTML: 598
  • CAUSES OF ADULT SPLANCHNIC VEIN THROMBOSIS IN THE MEDITERRANEAN AREA

    Valerio De Stefano, Tommaso Za, Angela Ciminello, Laura Betti, Elena Rossi
    e2011063
    2011-12-19
    https://doi.org/10.4084/mjhid.2011.063
    2546
    PDF: 875
    HTML: 3613
  • 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
    3464
    PDF: 958
    HTML: 391
    Table 1.: 215
  • A CASE SERIES HIGHLIGHTING THE RELATIVE FREQUENCY OF COMMON, UNCOMMON AND ATYPICAL/UNUSUAL HEMATOLOGICAL FINDINGS ON BONE MARROW EXAMINATION IN CASES OF VISCERAL LEISHMANIASIS

    Prateek Bhatia, Dipanjan Haldar, Neelam Varma, RK Marwaha, Subhash Varma
    e2011035
    2011-09-08
    https://doi.org/10.4084/mjhid.2011.035
    1336
    PDF: 594
    HTML: 3455
    Figures Leismania: 160
  • SYSTEMIC MASTOCYTOSIS: MULTIDISCIPLINARY APPROACH Systemic Mastocytosis

    Roberta Zanotti, Massimiliano Bonifacio, Ilaria Tanasi, Donatella Schena, Giovanni Orsolini, Morena Tebaldi, Lara Crosera, Francesca Mastropaolo, Elisa Olivieri, Dr. Patrizia Bonadonna
    e2021068
    2021-10-29
    https://doi.org/10.4084/MJHID.2021.068
    1465
    PDF: 909
    HTML: 213
  • OMENTAL SPLENOSIS MIMICKING PERITONEAL CARCINOMATOSIS

    Andrea Piccin
    e2026038
    2026-04-30
    https://doi.org/10.4084/MJHID.2026.038
    44
    PDF: 54
    HTML: 6
  • Bone marrow involvement in a patient with alpha heavy chain disease:Response to tetracycline treatment

    Zahit Bolaman, Irfan Yavasoglu, Gokhan Sargin, Gurhan Kadikoylu, Firuzan Kacar Doger
    e2012034
    2012-05-07
    https://doi.org/10.4084/mjhid.2012.034
    1179
    PDF: 998
    HTML: 3386
  • DIAGNOSIS AND PROGNOSIS EVALUATION OF SEVERE PNEUMONIA BY LUNG ULTRASOUND SCORE COMBINED WITH SERUM INFLAMMATORY MARKERS.

    Bo Fu, Peng Zhang, JunHua Zhang
    e2023057
    2023-10-30
    https://doi.org/10.4084/MJHID.2023.057
    756
    PDF: 542
    HTML: 124
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