Mediterranean Journal of Hematology and Infectious Diseases

Abstract 2007 | PDF Downloads 624 HTML Downloads 14831 Therapeutic Value of Combined Therapy with Deferasirox and Silymarin on Iron Overload in Children with Beta Thalassemia Downloads 0

Page e2013065

PDF HTML Therapeutic Value of Combined Therapy with Deferasirox and Silymarin on Iron Overload in Children with Beta Thalassemia

DOI: https://doi.org/10.4084/mjhid.2013.065

INFECTIONS IN THALASSEMIA AND HEMOGLOBINOPATHIES

Bianca Maria Ricerca, Arturo Di Girolamo, Deborah Rund

Abstract 880 | PDF Downloads 488 HTML Downloads 4167

Page e2009028

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THALASSAEMIA INTERMEDIA : AN UPDATE

Ali Taher, Khaled M. Musallam, Maria Domenica Cappellini

Abstract 843 | PDF Downloads 360 HTML Downloads 9230

Page e2009004

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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

Abstract 3672 | PDF Downloads 691 HTML Downloads 2378 Figures Downloads 0

Page e2016004

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DOI: https://doi.org/10.4084/mjhid.2016.004

VITAMIN D STATUS IN THALASSEMIA MAJOR: AN UPDATE

Ashraf Tawfik Soliman

Abstract 1950 | PDF Downloads 887 HTML Downloads 2391

Page e2013057

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DOI: https://doi.org/10.4084/mjhid.2013.057

THALASSAEMIA AND ABERRATIONS OF GROWTH AND PUBERTY

Andreas Kyriakou, Nicos Skordis

Abstract 868 | PDF Downloads 378 HTML Downloads 3130

Page e2009003

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THE ICET-A SURVEY ON CURRENT CRITERIA USED BY CLINICIANS FOR THE ASSESSMENT OF CENTRAL ADRENAL INSUFFICIENCY IN THALASSEMIA: ANALYSIS OF RESULTS AND RECOMMENDATIONS

Vincenzo De Sanctis

Abstract 3363 | PDF Downloads 635 HTML Downloads 1647

Page e2016034

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DOI: https://doi.org/10.4084/mjhid.2016.034

INSULIN-LIKE GROWTH FACTOR-1 (IGF-1): DEMOGRAPHIC, CLINICAL AND LABORATORY DATA IN 120 CONSECUTIVE ADULT PATIENTS WITH THALASSAEMIA MAJOR

V. De Sanctis

Abstract 1908 | PDF Downloads 730 HTML Downloads 26775

Page e2014.074

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DOI: https://doi.org/10.4084/mjhid.2014.074

ASSOCIATION OF VDBP RS4701 VARIANT, BUT NOT VDR/RXR-? OVER-EXPRESSION WITH BONE MINERAL DENSITY IN PEDIATRIC ?-THALASSEMIA PATIENTS

Shaimaa Sahmoud, Mostafa S. Ibrahim, Eman A. Toraih, Noha Kamel, Manal Fawzy, Samar Elfiky

Abstract 936 | PDF Downloads 589 HTML Downloads 148

Page e2020037

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DOI: https://doi.org/10.4084/mjhid.2020.037

Thalassemia carrier detection among pregnant women

Edhyana Sahiratmadja, Merry M.V. Seu, Ita M. Nainggolan, Johanes C. Mose, Ramdan Panigoro

Abstract 1213 | PDF Downloads 433 HTML Downloads 165

Page e2021003

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DOI: https://doi.org/10.4084/mjhid.2021.003

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

Abstract 1895 | PDF Downloads 1032 HTML Downloads 161

Page e2019013

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DOI: https://doi.org/10.4084/mjhid.2019.013

CAN WE PREDICT INCIPIENT DIABETES MELLITUS IN PATIENTS WITH TRANSFUSION DEPENDENT β-THALASSEMIA (β-TDT) REFERRED WITH A HISTORY OF PREDIABETES?

Vincenzo De Sanctis, Ashraf Soliman, Shahina Daar, Ploutarchos Tzoulis, Christos Kattamis

Abstract 764 | PDF Downloads 1156 HTML Downloads 67

Page e2024005

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DOI: https://doi.org/10.4084/MJHID.2024.005

The INFLUENCE OF NUTRITION ON DISEASE SEVERITY AND HEALTH-RELATED QUALITY OF LIFE IN ADULTS WITH SICKLE CELL DISEASE

Sanaa Kamal, Moheyeldeen Mohamed Naghib, Jamaan Al Zahrani, Huda Hassan, Karim Abdel Aziz Moawado, Omar Arrahman

Abstract 1678 | PDF Downloads 714 HTML Downloads 186

Page e2021007

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DOI: https://doi.org/10.4084/mjhid.2021.007

ADVERSE PREGNANCY OUTCOMES IN SICKLE CELL TRAIT: A PROSPECTIVE COHORT STUDY EVALUATING CLINICAL AND HAEMATOLOGICAL PARAMETERS IN POSTPARTUM MOTHERS AND NEW-BORNS.

r. Salam Al-Kindi

Abstract 914 | PDF Downloads 1017 HTML Downloads 360

Page e2023002

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DOI: https://doi.org/10.4084/MJHID.2023.002

PERIOPERATIVE MANAGEMENT OF SICKLE CELL DISEASE: A NARRATIVE REVIEW

Kwame Ofori Adjepong, Folashade Otegbeye, Yaw Amoateng ADJEPONG

Abstract 7064 | PDF Downloads 2881 HTML Downloads 905

Page e2018032

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DOI: https://doi.org/10.4084/mjhid.2018.032

PATHOPHISIOLOGY OF SICKLE CELL DISEASE AND NEW DRUGS FOR THE TREATMENT

Lucia De Franceschi

Abstract 807 | PDF Downloads 563 HTML Downloads 10907

Page e2009024

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NEW THERAPEUTIC OPTIONS FOR THE TREATMENT OF SICKLE CELL DISEASE

Alessandro Matte, Filippo Mazzi, Enrica Federti, Oliviero Olivieri, Lucia De Franceschi

Abstract 5804 | PDF Downloads 3212 HTML Downloads 531

Page e2019002

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DOI: https://doi.org/10.4084/mjhid.2019.002

A novel ALAS2 mutation causes congenital sideroblastic anemia

Kun Yang

Abstract 325 | PDF Downloads 311 HTML Downloads 74

Page e2023062

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DOI: https://doi.org/10.4084/MJHID.2023.062

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

Abstract 372 | PDF Downloads 938 HTML Downloads 51

Page e2024023

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

PROTECTIVE ROLE OF SYLIMARIN ON METHOTREXATE INDUCED HEPATO-NEPHROTOXICITY IN CHILDREN WITH ACUTE LYMPHOBLASTIC LEUKEMIA

Adel Abd Elhaleim Hagag

Abstract 3146 | PDF Downloads 828 HTML Downloads 1036

Page e2016043

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DOI: https://doi.org/10.4084/mjhid.2016.043

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