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The COST-UTILITY ANALYSIS OF FOUR CHELATION REGIMENS FOR ?-THALASSEMIA MAJOR: A CHINESE PERSPECTIVE

Jialian Li

e2020029

2020-04-27

https://doi.org/10.4084/mjhid.2020.029

1977

PDF: 1002

HTML: 349
MODULATING EFFECT OF THE ?158 G? (C?T) XMN-1 POLYMORPHISM IN INDIAN SICKLE CELL PATIENTS

Sanjay Pandey, Sweta Pandey, Rahasya Mani Mishra, Renu Saxena

e2012001

2012-01-15

https://doi.org/10.4084/mjhid.2012.001

1630

PDF: 930

HTML: 1446

Table: 214
EFFICACY AND SAFETY OF SINOPHARM VACCINE FOR SARS-COV-2 AND BREAKTHROUGH INFECTIONS IN IRANIAN PATIENTS WITH HEMOGLOBINOPATHIES: A PRELIMINARY REPORT Sinopharm Vaccination in Iranian Patients with Hemoglobinopathies

Mehran Karimi, Tahereh Zarei, Sezaneh Haghpanah , Azita Azarkeiva, Maryam Naderi , Sara Matin , Asghar Bazrafshan , Zohreh Zahedi , Afshan Shirkavand , Parisa pishdad, Vincenzo De Sanctis

e2022026

2022-02-27

https://doi.org/10.4084/MJHID.2022.026

1770

PDF: 766

HTML: 239
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

390

PDF: 264

Html: 155
Protein S deficiency with recurrent thromboembolism in a patient with hemoglobin H disease following splenectomy

Kun Yang

e2024017

2024-02-29

https://doi.org/10.4084/MJHID.2024.017

663

PDF: 1096

HTML: 122
Does splenectomy influence the development of Hypothyroidism in Transfusion Dependent Thalassemia Patients? A retrospective study. Splenectomy in Hypothyroidism of TDT patients

Christos KATTAMIS, Myrto Skafida, Christalena Sofocleous, Antonis Kattamis

e2019064

2019-10-30

https://doi.org/10.4084/mjhid.2019.064

1310

PDF: 988

HTML: 337
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

1531

PDF: 633

HTML: 384
THALIDOMIDE AMELIORATES ERYTHROPOIESIS AND IRON HOMEOSTASIS IN TRANSFUSION-DEPENDENT β-THALASSEMIA Thalidomide ameliorates erythropoiesis and iron homeostasis

Kun Yang, Jian Xiao

e2024001

2024-01-01

https://doi.org/10.4084/MJHID.2024.001

1501

PDF: 1470

PDF: 1045

HTML: 231
SEVERE LIVER IRON CONCENTRATIONS (LIC) IN 24 PATIENTS WITH ?-THALASSEMIA MAJOR: CORRELATIONS WITH SERUM FERRITIN, LIVER ENZYMES AND ENDOCRINE COMPLICATIONS

Vincenzo De Sanctis

e2018062

2018-10-27

https://doi.org/10.4084/mjhid.2018.062

2828

PDF: 1442

HTML: 367
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

2260

PDF: 1023

HTML: 3067

Untitled: 242
Late-onset male hypogonadism and fertility potential in thalassemia major patients: Two emerging issues

Vincenzo De Sanctis

e2015047

2015-07-08

https://doi.org/10.4084/mjhid.2015.047

1853

PDF: 973

HTML: 844
CORRELATION OF TRANSIENT ELASTOGRAPHY WITH LIVER IRON CONCENTRATION, AND SERUM FERRITIN LEVELS IN PATIENTS WITH TRANSFUSION-DEPENDENT THALASSEMIA MAJOR PATIENTS FROM OMAN

Hammad Khan, Vinodh Panjwani, Sara Al Rahbi, Abubakr Eltigani , Rizwan Qureshi, Khaleeq Unnisa, Najmus Sehar, Alok Mittal, Anil Pathare

e2023048

2023-08-29

https://doi.org/10.4084/MJHID.2023.048

1216

PDF: 733

HTML: 251
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

1798

PDF: 955

HTML: 1621
Luspatercept Treatment in a β-Thalassemia Patient with Pulmonary Arterial Hypertension: A Case Report

beibei yang, dongmei liu, changyu yang, Yali zhou, Guiping Liao, jian huang, Yingying Li, yinjiang tang, xiaolin yin

e2025059

2025-08-31

https://doi.org/10.4084/MJHID.2025.059

1256

PDF: 635

Html: 199
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

611

PDF: 1112

HTML: 107
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

1420

PDF: 700

HTML: 404
ACTIVIN RECEPTOR LIGAND FOR THR TREATMENT OF BETA-THALASSEMIA: a SERENDIPITOUS DISCOVERY

Irene Motta, Valentina Brancaleoni, Isabella Nava, Paola Delbini, Lorena Duca

e2020075

2020-10-27

https://doi.org/10.4084/mjhid.2020.075

1697

PDF: 1477

HTML: 616
Prospective, case-control study of serological response after two doses of BNT162b2 anti-SARS-CoV-2 mRNA vaccine in transfusion-dependent thalassemic patients

NICOLA SGHERZA, Stefania Zucano, Angelantonio Vitucci, Antonio Palma, Francesco Tarantini, Daniela Campanale, Luigi Vimercati, Angela Maria Vittoria Larocca, Domenico Visceglie, Amalia Acquafredda, Angelo Ostuni, Daniela Di Gennaro, Carmen Vitucci, Silvio Tafuri, Pellegrino Musto

e2022056

2022-06-29

https://doi.org/10.4084/MJHID.2022.056

1237

HTML: 310

PDF: 532
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

2813

PDF: 1690

HTML: 289
SICKLE CELL DISEASE AND VENOUS THROMBOEMBOLISM

Zohreh Rahimi, Abbas Parsian

e2011024

2011-05-23

https://doi.org/10.4084/mjhid.2011.024

2351

PDF: 947

HTML: 2220
CURRENT ISSUES AND OPTIONS FOR HORMONAL CONTRACEPTION IN ADOLESCENTS AND YOUNG ADULT WOMEN WITH SICKLE CELL DISEASE: AN UPDATE FOR HEALTH CARE PROFESSIONALS Hormonal Contraception in Adolescents and Young Adult Women With Sickle Cell Disease

Vincenzo De Sanctis

e2020032

2020-04-27

https://doi.org/10.4084/mjhid.2020.032

2281

PDF: 1480

HTML: 971
How we prevented an anti-P1 mediated hemolytic transfusion reaction

Beatrice Borsellino, Tiziano Martini, Rino Biguzzi, Irene Francesconi, Maria Federica Currà, Sabrina Lelli

e2024009

2024-01-01

https://doi.org/10.4084/MJHID.2024.009

1238

PDF: 1273

HTML: 518
Liver iron concentration and liver impairment in relation to serum IGF-1 levels in thalassaemia major patients: A retrospective study

Vincenzo De Sanctis, Ashraf T Soliman, Giancarlo Candini, Christos Kattamis, Giuseppe Raiola, Heba Elsedfy

e2015016

2015-02-13

https://doi.org/10.4084/mjhid.2015.016

1673

PDF: 1080

HTML: 880

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Search

Search Results

The COST-UTILITY ANALYSIS OF FOUR CHELATION REGIMENS FOR ?-THALASSEMIA MAJOR: A CHINESE PERSPECTIVE

MODULATING EFFECT OF THE ?158 G? (C?T) XMN-1 POLYMORPHISM IN INDIAN SICKLE CELL PATIENTS

EFFICACY AND SAFETY OF SINOPHARM VACCINE FOR SARS-COV-2 AND BREAKTHROUGH INFECTIONS IN IRANIAN PATIENTS WITH HEMOGLOBINOPATHIES: A PRELIMINARY REPORT Sinopharm Vaccination in Iranian Patients with Hemoglobinopathies

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

Protein S deficiency with recurrent thromboembolism in a patient with hemoglobin H disease following splenectomy

Does splenectomy influence the development of Hypothyroidism in Transfusion Dependent Thalassemia Patients? A retrospective study. Splenectomy in Hypothyroidism of TDT patients

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

THALIDOMIDE AMELIORATES ERYTHROPOIESIS AND IRON HOMEOSTASIS IN TRANSFUSION-DEPENDENT β-THALASSEMIA Thalidomide ameliorates erythropoiesis and iron homeostasis

SEVERE LIVER IRON CONCENTRATIONS (LIC) IN 24 PATIENTS WITH ?-THALASSEMIA MAJOR: CORRELATIONS WITH SERUM FERRITIN, LIVER ENZYMES AND ENDOCRINE COMPLICATIONS

THE ROLE OF THE CAROTID DOPPLER EXAMINATION IN THE EVALUATION OF ATHEROSCLEROTIC CHANGES IN BETA THALASSEMIA PATIENTS

Late-onset male hypogonadism and fertility potential in thalassemia major patients: Two emerging issues

CORRELATION OF TRANSIENT ELASTOGRAPHY WITH LIVER IRON CONCENTRATION, AND SERUM FERRITIN LEVELS IN PATIENTS WITH TRANSFUSION-DEPENDENT THALASSEMIA MAJOR PATIENTS FROM OMAN

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

Luspatercept Treatment in a β-Thalassemia Patient with Pulmonary Arterial Hypertension: A Case Report

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

Formulas for the Detection ?-Thalassemia Carriers Are Affected by Changes in Red Cell Parameters

ACTIVIN RECEPTOR LIGAND FOR THR TREATMENT OF BETA-THALASSEMIA: a SERENDIPITOUS DISCOVERY

Prospective, case-control study of serological response after two doses of BNT162b2 anti-SARS-CoV-2 mRNA vaccine in transfusion-dependent thalassemic patients

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

SICKLE CELL DISEASE AND VENOUS THROMBOEMBOLISM

CURRENT ISSUES AND OPTIONS FOR HORMONAL CONTRACEPTION IN ADOLESCENTS AND YOUNG ADULT WOMEN WITH SICKLE CELL DISEASE: AN UPDATE FOR HEALTH CARE PROFESSIONALS Hormonal Contraception in Adolescents and Young Adult Women With Sickle Cell Disease

How we prevented an anti-P1 mediated hemolytic transfusion reaction

Liver iron concentration and liver impairment in relation to serum IGF-1 levels in thalassaemia major patients: A retrospective study

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