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Editor-in-Chief: Giuseppe Leone | Italy

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  • PREVALENCE OF SICKLE CELL TRAIT IN THE SOUTHERN SUBURBS OF BEIRUT, LEBANON

    Abdel Badih El Ariss, Mohamad Younes, Jad Matar, Zeina Berjaoui
    e2016015
    2016-02-20
    https://doi.org/10.4084/mjhid.2016.015
    4300
    PDF: 1073
    HTML: 19265
  • MOLECULAR HETEROGENEITY OF GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY IN BURKINA FASO: G-6-PD BETICA SELMA AND SANTAMARIA IN PEOPLE WITH SYMPTOMATIC MALARIA IN OUAGADOUGOU

    Abdoul Karim OUATTARA, Pouiré YAMEOGO, Birama DIARRA, Dorcas OBIRI-YEBOAH, Albert Theophane YONLI, Tegwindé Rebeca COMPAORE, Serge Théophile SOUBEIGA, Florencia Wenkuuni DJIGMA, Jacques Simpore
    e2016029
    2016-06-15
    https://doi.org/10.4084/mjhid.2016.029
    4325
    PDF: 1130
    HTML: 1421
  • HbD Punjab/HbQ India compound heterozygosity: An unusual association.

    Stacy Colaco, Reema Surve, Pratibha Sawant, Anita Nadkarni, Kanjaksha Ghosh, Roshan Colah
    e2014072
    2014-11-01
    https://doi.org/10.4084/mjhid.2014.072
    1644
    PDF: 868
    HTML: 5627
  • PREVALENCE OF THALASSEMIA AMONG NEWBORNS: A RE-VISITED AFTER 20 YEARS OF A PREVENTION AND CONTROL PROGRAM IN NORTHEAST THAILAND.

    Goonnapa Fucharoen
    e2018054
    2018-09-01
    https://doi.org/10.4084/mjhid.2018.054
    1919
    PDF: 1180
    HTML: 274
  • CRYOGLOBULIN TEST AND CRYOGLOBULINEMIA HEPATITIS C-VIRUS RELATED

    Umberto Basile
    e2017007
    2017-01-01
    https://doi.org/10.4084/mjhid.2017.007
    4504
    PDF: 1416
    HTML: 2610
  • MOLECULAR CHARACTERIZATION OF EPSTEIN - BARR VIRUS BASED ON EBNA3C PROTEIN AMONG HEMATOPOIETIC STEM CELL TRANSPLANT RECIPIENTS IN JORDAN

    Rabaa Athamneh, Hiba Swaity, Waleed Almomani, Hayyan. Taweil , Assia Benbraiek, Anas Khalifeh
    e2025032
    2025-04-30
    https://doi.org/10.4084/MJHID.2025.032
    938
    PDF: 934
    HTML: 139
  • SICKLE CELL TRAIT, CLINICAL MANIFESTATIONS AND OUTCOMES: A CROSS-SECTIONAL STUDY

    Diego A Vargas-Hernández, Adriana Catalina Uscategui-Ruiz, Andrés Jesus Prada-Rueda , Consuelo Romero-Sánchez
    e2023015
    2023-02-28
    https://doi.org/10.4084/MJHID.2023.015
    1957
    PDF: 1202
    HTML: 538
  • SPECTRUM OF BETA GLOBIN GENE MUTATIONS IN EGYPTIAN CHILDREN WITH ?- THALASSEMIA

    MR El-Shanshory, Adel Abd Elhaleim Hagag
    e2014071
    2014-08-28
    https://doi.org/10.4084/mjhid.2014.071
    2155
    PDF: 1106
    HTML: 4301
  • Leukocyte derived chemotaxin 2 (ALECT2) amyloidosis

    Uday P Kulkarni, Anna Valson, Anila Korula, Vikram Mathews
    e2015043
    2015-07-01
    https://doi.org/10.4084/mjhid.2015.043
    1731
    PDF: 845
    HTML: 1343
  • THE EFFECT OF ALPHA THALASSEMIA, HBF and HBC ON HAEMATOLOGICAL PARAMETERS OF SICKLE CELL DISEASE PATIENTS IN IBADAN, NIGERIA. ALPHA THALASSEMIA, HBF and HBC ON HAEMATOLOGICAL PARAMETERS OF SICKLE CELL DISEASE PATIENTS

    FASOLA ATINUKE
    e2022001
    2022-01-01
    https://doi.org/10.4084/MJHID.2022.001
    3085
    PDF: 1091
    HTML: 190
  • HAPTOGLOBIN PHENOTYPES AND SUSCEPTIBILITY OF SCHISTOSOMA PARASITES INFECTION IN CENTRAL SUDAN

    Ashraf Siddig Yousif, Atif Abdelrahman Elagib
    e2017042
    2017-07-01
    https://doi.org/10.4084/mjhid.2017.042
    2492
    PDF: 814
    HTML: 1079
  • HEMATOPOIETIC STEM CELL TRANSPLANTATION IN SEVERE PEDIATRIC SICKLE CELL DISEASE: OUTCOME AND LONG-TERM COMPLICATIONS, SAUDI EXPERIENCE AT KING FAISAL SPECIALIST HOSPITAL, RIYADH, SAUDI ARABIA HCT in in Severe Pediatric Sickle Cell Disease

    Abdullah Al-Jefri, Fatema Al-Hashem, Khawar, Amal Al-Seraihy, Ali Al-Ahmari, Ibrahim Ghemlas, Awatif AlAnazi, Hawazen Al-Saedi, Saadiya Khan, Abdulrahman Al-Musa, Mahasen Saleh, Mouhab Ayas
    e2025030
    2025-04-30
    https://doi.org/10.4084/MJHID.2025.030
    1435
    PDF: 1035
    HTML: 515
  • Multiple myeloma diagnosed by CT-guided rib biopsy after a hemodilute bone marrow aspirate, in a patient with a biclonal pattern on serum protein electrophoresis Multiple Myeloma diagnosed with CT-guided rib biopsy

    Arjeta Cyrbja, Liri Seraj, Shaqir Qerama
    e2026061
    2026-06-30
    https://doi.org/10.4084/MJHID.2026.061
    263
    PDF: 142
    HTML: 279
  • PRENATAL DIAGNOSIS OF ?-THALASSEMIAS AND HEMOGLOBINOPATHIES

    Maria Cristina Rosatelli, Luisella Saba
    e2009011
    2009-11-15
    1942
    PDF: 417
    HTML: 6532
  • PROLIFERATION AND APOPTOSIS OF B-CELL LYMPHOMA CELLS UNDER TARGETED REGULATION OF FOXO3 BY miR-155 miR-155, FOXO3, B-cell lymphoma, proliferation, apoptosis, clinical characteristics

    Xiaoqiang Zheng, Hongbing Rui, Ying Liu, Jinfeng Dong
    e2020073
    2020-11-02
    https://doi.org/10.4084/mjhid.2020.073
    938
    PDF: 167
    HTML: 231
  • 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
    6935
    PDF: 1742
    HTML: 1635
  • NON-SECRETORY MYELOMA: READY FOR A NEW DEFINITION?

    Alessandro Corso, Silvia Mangiacavalli
    e2017053
    2017-08-18
    https://doi.org/10.4084/mjhid.2017.053
    3421
    PDF: 1791
    HTML: 1179
  • A strange case of Malaria in a Nigerian native boy.

    Paola Magro, Ilaria Izzo, Barbara Saccani, Salvatore Casari, Silvio Caligaris, Lina Rachele Tomasoni, Alberto Matteelli, Annamaria Lombardi, Antonella Meini, Francesco Castelli
    e2017023
    2017-03-01
    https://doi.org/10.4084/mjhid.2017.023
    2620
    PDF: 932
    HTML: 1341
  • DETECTION OF ? THALASSEMIA CARRIERS BY RED CELL PARAMETERS OBTAINED FROM AUTOMATIC COUNTERS USING MATHEMATICAL FORMULAS

    Idit Lachover Roth, Boaz Lachover, Guy Koren, Carina Levin, Luci Zalman, Ariel Koren
    e2018008
    2018-01-01
    https://doi.org/10.4084/mjhid.2018.008
    5091
    PDF: 1810
    HTML: 1247
  • Gamma heavy chain disease associated with T-cell large granular lymphocyte lymphoproliferative disorder: case report and literature review.

    Maria Laura Bisegna, Maria Assunta Limongiello, Stefano Fiori, Maria Stefania De Propris, Irene Della Starza, Stefania Trasarti
    e2023010
    2023-01-01
    https://doi.org/10.4084/MJHID.2023.010
    1205
    PDF: 1018
    HTML: 488
  • NOVEL MUTATIONS IN THE NON-STRUCTURE PROTEIN 2 OF SARS-CoV-2 Sequence analysis NSP2 of SARS-CoV-2

    Mohsen Nakhaei, Zohreh-Al-Sadat Ghoreshi, Mohammad Rezaei Zadeh Rukerd, Hedyeh Askarpour, Nasir
    e2023059
    2023-10-16
    https://doi.org/10.4084/MJHID.2023.059
    1125
    PDF: 531
    HTML: 170
  • THE ROLE OF THE CAROTID DOPPLER EXAMINATION IN THE EVALUATION OF ATHEROSCLEROTIC CHANGES IN BETA THALASSEMIA PATIENTS

    Gehan Lotfy Abdel Hakeem, hoda Abdel kereem Abdel Samei, Ashraf mohamed El Shereif, Ahlam mohamed ismail
    e2015023
    2015-02-17
    https://doi.org/10.4084/mjhid.2015.023
    2311
    PDF: 1053
    HTML: 3073
    Untitled: 277
  • MOLECULAR HETEROGENEITY IN ACUTE PROMYELOCYTIC LEUKEMIA - A SINGLE CENTRE EXPERIENCE FROM INDIA

    Nikhil Rabade, Goutham Raval, Shruti Chaudhary, PG Subramanian, Rohan Kodgule, Swapnali Joshi, Prashant Tembhare, Hasmukh Jain, Manju Sengar, Syed Hasan K, Pratibha Amare Kadam, Dhanalaxmi Shetty, Gaurav Narula, Shripad Banavali, Sumeet Gujral, Nikhil Patkar
    e2018002
    2018-01-01
    https://doi.org/10.4084/mjhid.2018.002
    3783
    PDF: 1285
    HTML: 1127
  • 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
    2768
    PDF: 945
    HTML: 8001
    Untitled: 236
  • ASSESSMENT OF DIAGNOSTIC TECHNIQUES OF URINARY TUBERCULOSIS

    Khaled Ismail Ghaleb, Magdy Mohamed afifi, Mohamed Mohamed El Gohary
    e2013034
    2013-06-03
    https://doi.org/10.4084/mjhid.2013.034
    2869
    PDF: 847
    HTML: 2380
    Untitled: 259
  • Bilateral Pleural Effusions due to Pulmonary Amyloidosis as the Presenting Manifestation of Multiple Myeloma

    Abhishek Agarwal, Sandeep Singla, Meghana Bansal, Bijay Nair
    e2012010
    2012-01-25
    https://doi.org/10.4084/mjhid.2012.010
    1676
    PDF: 829
    HTML: 4426
    Figure 1: 198
    Untitled: 187
    Untitled: 240
  • 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
    10755
    PDF: 1056
    HTML: 315
  • Transfusion associated peak in Hb HPLC chromatogram – a case report

    Sonal Jain, Jasmita Dass, Hara Prasad Pati
    e2012006
    2012-01-21
    https://doi.org/10.4084/mjhid.2012.006
    1178
    PDF: 826
    HTML: 2822
  • 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
  • EPSTEIN-BARR VIRUS RELATED LYMPHOPROLIFERATIONS AFTER STEM CELL TRANSPLANTATION

    Simona Sica, Elisabetta Metafuni, Silvia Bellesi, Patrizia Chiusolo
    e2009019
    2009-12-14
    https://doi.org/10.4084/mjhid.2009.019
    1507
    PDF: 618
    HTML: 3053
  • Skin Involvement in Primary Systemic Amyloidosis

    susheel kumar
    e2013005
    2013-01-02
    https://doi.org/10.4084/mjhid.2013.005
    1757
    PDF: 953
    HTML: 4448
    Figure 1. Photographs showing (a) enlarged tongue with (b) teeth marks over the lateral margin and (c, d) multiple, papular lesions over lower chest wall: 229
    Figure 2. Microphotograph showing pink eosinophilic homogenous material in the dermis, H&E X 20: 206
    Figure 3. Pink eosinophilic material showing pale orange positivity with Congo red stain: 231
  • CLINICAL AND LABORATORY FEATURES OF SICKLE CELL DISEASE S/D PUNJAB: IMPACT OF HBF AND HYDROXYUREA SCD S/D Punjab

    r. Salam Al-Kindi, Isra Al-Busaidi, Anil Pathare
    e2024046
    2024-04-30
    https://doi.org/10.4084/MJHID.2024.046
    1448
    PDF: 1227
    HTML: 166
  • 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
  • EPIDEMIOLOGY OF METHICILLIN RESISTANT STAPHYLOCOCCUS AUREUS IN ARAB COUNTRIES OF THE MIDDLE EAST AND NORTH AFRICAN REGION

    Hussam Tabaja, Dr. Joya-Rita Hindy, Dr. Souha S. Kanj
    e2021050
    2021-08-28
    https://doi.org/10.4084/MJHID.2021.050
    2714
    PDF: 1056
    HTML: 487
  • 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
    3434
    PDF: 673
    Suppl. Files: 330
    HTML: 312
  • 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
    4200
    PDF: 933
    HTML: 1550
  • Clinical and Hematological Characteristics of Vietnamese Heterozygous Hb Tak/β-Thalassemia Patients: A Four- Case Series

    Ngoc Dung Nguyen, Thi Chi Nguyen, Thi Thu Ha Nguyen, Thi Nguyet Anh Phi, Xuan Hai Le, Duc Luong Vu
    e2026024
    2026-02-28
    https://doi.org/10.4084/MJHID.2026.24
    632
    PDF: 504
    HTML: 434
  • 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
  • INFLUENCE OF SICKLE CELL GENE ON THE ALLELIC DIVERSITY AT THE MSP-1 LOCUS OF PLASMODIUM FALCIPARUM IN ADULT PATIENTS WITH SEVERE MALARIA

    Dilip Kumar Patel, Ranjeet Singh Mashon, Prasanta Purohit, Siris Patel, Satyabrata Meher, Snehadhini Dehury, Chhatray Marndi, Kishalaya Das, Bipin Kishore Kullu, Padmalaya Das
    e2015050
    2015-08-24
    https://doi.org/10.4084/mjhid.2015.050
    1653
    PDF: 959
    HTML: 6441
  • Bortezomib maintenance for the treatment of Monoclonal Gammopathy of Renal Significance

    Holly Lee, Peter Duggan, Ernesta Paola Neri, Jason Tay, Victor Jimenez Zepeda
    e2019007
    2019-01-01
    https://doi.org/10.4084/mjhid.2019.007
    2444
    PDF: 1233
    HTML: 425
  • 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
    2186
    PDF: 969
    HTML: 1917
  • IDENTİFİCATİON OF LEİSHMANİA TROPİCA FROM PEDİATRİC VİSCERAL LEİSHMANİASİS İN SOUTHERN MEDITERRANEAN REGION OF TURKEY. Molecular characterization of pediatric visceral leishmaniasis

    Derya Alabaz, Fadime Eroğlu, Hüseyin Elçi, Ümmühan Çay
    e2022053
    2022-06-29
    https://doi.org/10.4084/MJHID.2022.053
    1188
    PDF: 778
    HTML: 288
  • miR-155-5p PROMOTES CD34+ APOPTOSIS AND INHIBITS BONE MARROW HEMATOPOIESIS IN MYELODYSPLASTIC SYNDROMES BY RAC1/CREB/MIR-15B AXIS

    Meiwan Cao, BaoLing Peng, WanFu Xu, PeiYu Chen, Huan Chen, LiPing Ye, Jing Xie, HongLi Wang, Lu Ren, LiYa Xiong, JingNan Zhu, XiangYe Xu, LanLan Geng, SiTang Gong
    e2023040
    2023-06-29
    https://doi.org/10.4084/MJHID.2023.040
    858
    PDF: 951
    PDF Supp. Files: 112
    HTML: 265
  • 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
  • The IMPACT OF SUPEROXIDE DISMUTASE GENETIC POLYMORPHISM (SOD2 VAL16ALA) AND SUPEROXIDE DISMUTASE LEVEL ON DISEASE SEVERITY IN A COHORT OF EGYPTIAN SICKLE CELL DISEASE PATIENTS IN EGYPT SOD and SCD in Egypt

    Mervat Khorshied, Iman A, Shaheen, Yasmeen M.M Selim, Asmaa O. Elshahawy, Ilham Youssry
    e2022037
    2022-04-28
    https://doi.org/10.4084/MJHID.2022.037
    1248
    PDF: 670
    HTML: 515
  • 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
    1939
    PDF: 555
    HTML: 380
  • COMPREHENSIVE REVIEW OF GENETIC AND EPIGENETICS REGULATION OF FETAL HEMOGLOBIN IN β-HEMOGLOBINOPATHIES: FROM MOLECULAR MECHANISMS TO CLINICAL APPLICATIONS HbF Genetics in Anemia

    Yousef Saeed Mohammad Abu Za’ror, Joseph Bagi Suleiman, Fatima Azzahra Delmani, Jehad Farouq Alhmoud, Amer Mohammad Ayasreh, Sarah Ihsan Al-wendawi, Maryam Azlan
    e2026046
    2026-04-30
    https://doi.org/10.4084/MJHID.2026.046
    994
    PDF: 701
    HTML: 145
  • THE CLINICAL SIGNIFICANCE OF THE SPECTRUM OF INTERACTIONS OF THE RARE IVS-II-5 G>C (HBB: C.315+5 G>C) VARIATION WITH OTHER Β-THALASSEMIA MUTATIONS IN SOUTHERN CHINA

    Yali Zhou, Guiping Liao, Xiaolin Yin, Sheng He, Yi Wu, Jian Xiao, Zhili Geng, Qiuying Huang, Ganghui Luo, Kun Yang
    e2022034
    2022-04-28
    https://doi.org/10.4084/MJHID.2022.034
    1596
    PDF: 671
    HTML: 406
  • ASSOCIATION OF BASELINE PLATELET COUNT WITH COMPLETE REMISSION, SEVERE BLEEDING, AND 24-MONTH OVERALL SURVIVAL IN PATIENTS WITH NEWLY DIAGNOSED ACUTE MYELOID LEUKEMIA: A SINGLE-CENTER RETROSPECTIVE COHORT STUDY

    Tao Zhou, Zengfeng Ni, Wenjing Fan, Jing Xu, Jing Qin, Kaiyue Wang, Rui Wang, Yaping Li
    e2026071
    2026-09-01
    https://doi.org/10.4084/MJHID.2026.071
    132
    PDF: 99
    Suppl. Files: 23
    Html: 23
    Html Suppl. Files: 22
  • CURRENT STRATEGIES FOR THE DETECTION OF MINIMAL RESIDUAL DISEASE IN CHILDHOOD ACUTE LYMPHOBLASTIC LEUKEMIA

    Juliana Maria Camargos Rocha, Sandra Guerra Xavier, Marcelo Eduardo Lima Souza, Juliana Godoy Assumpção, Mitiko Murao, Benigna Maria Oliveira
    e2016024
    2016-04-10
    https://doi.org/10.4084/mjhid.2016.024
    4819
    PDF: 1411
    HTML: 4959
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