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• SERUM TOTAL BILIRUBIN, NOT CHOLELITHIASIS, IS INFLUENCED BY UGT1A1 POLYMORPHISM, ALPHA THALASSEMIA AND ?S GENOTYPE: FIRST REPORT ON COMPARISON BETWEEN ARAB-INDIAN AND AFRICAN ?S GENES

  Said Y ALkindi, Anil Pathare, Salam Alkindi

  e2015060

  2015-10-20

  https://doi.org/10.4084/mjhid.2015.060

  1833

  PDF: 986

  HTML: 1638

• 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: 1226

  HTML: 165

• THALASSAEMIA INTERMEDIA : AN UPDATE

  Ali Taher, Khaled M. Musallam, Maria Domenica Cappellini

  e2009004

  2009-08-17

  1150

  PDF: 479

  HTML: 9481

• Clinical spectrum and genotypes of children with alpha-thalassemia in northeastern, Thailand

  Patcharee Komvilaisak, Nattakarn Sangkha, Arunee Jetsrisuparp, Kunanya Suwannaying, Goonnapa Fucharoen, Napat Laoaroon

  e2025081

  2025-10-31

  https://doi.org/10.4084/MJHID.2025.081

  426

  PDF: 287

  Html: 201

• REVIEW AND RECOMMENDATIONS ON MANAGEMENT OF ADULT FEMALE THALASSEMIA PATIE?TS WITH HYPOGONADISM BASED ON LITERATURE REVIEW AND EXPERIENCE OF ICET-A NETWORK SPECIALISTS

  Vincenzo De Sanctis

  e2017001

  2017-01-01

  https://doi.org/10.4084/mjhid.2017.001

  6421

  PDF: 1514

  HTML: 2046

• FINAL HEIGHT AND ENDOCRINE COMPLICATIONS IN PATIENTS WITH ?-THALASSSEMIA INTERMEDIA: OUR EXPERIENCE IN NON-TRANSFUSED VERSUS INFREQUENTLY TRANSFUSED PATIENTS AND CORRELATIONS WITH LIVER IRON CONTENT None

  Vincenzo De Sanctis, Mohamed Yassin

  e2019026

  2019-04-25

  https://doi.org/10.4084/mjhid.2019.026

  2871

  PDF: 1722

  HTML: 300

• 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

  3719

  PDF: 1055

  HTML: 484

  Table 1.: 283

• Effectiveness and Safety of Sitagliptin in Patients with Beta-thalassaemia Major and Diabetes Mellitus: A Case Series

  Shahrzad Zonoozi

  e2017004

  2017-01-01

  https://doi.org/10.4084/mjhid.2017.004

  3074

  PDF: 1050

  HTML: 1307

• Could the 3′UTR+101G>C Mutation Detected in Two Sibling Cases Be a Mutation Affecting the Clinical Presentation in Thalassemia Patients?

  Unal Atas, Volkan Karakus, Erdal Kurtoglu

  e2024023

  2024-02-29

  https://doi.org/10.4084/MJHID.2024.023

  637

  PDF: 1149

  HTML: 119

• 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

  2173

  PDF: 1119

  HTML: 15744

  COVER LETTER: 244

• HEALTH-RELATED QUALITY OF LIFE IN THAI CHILDREN WITH THALASSEMIA AS EVALUATED BY PEDSQL AND EQ-5D-Y: A SINGLE CENTER EXPERIENCE

  Pacharapan Surapolchai, Phakatip Sinlapamongkolkul

  e2020036

  2020-06-28

  https://doi.org/10.4084/mjhid.2020.036

  1675

  PDF: 1230

  HTML: 388