Literature DB >> 12580361

Thalassemia: current approach to an old disease.

Louise Lo1, Sylvia Titi Singer.   

Abstract

This article discusses the approach for recognition, diagnosis, and management of the thalassemias, and reviews new prospects of therapy, focusing mostly on the beta-thalassemias--the more severe and clinically important type, beta-thalassemia major is typically treated with regular transfusion and chelation therapy. New strategies for specific therapy including monitoring of iron induced organ damage, fetal hemoglobin augmentation as an alternative for transfusions, bone marrow transplantation offer hope for prevention of complications and better care of the beta-thalassemias.

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Year:  2002        PMID: 12580361     DOI: 10.1016/s0031-3955(02)00088-3

Source DB:  PubMed          Journal:  Pediatr Clin North Am        ISSN: 0031-3955            Impact factor:   3.278


  8 in total

1.  Evaluation of growth, puberty and endocrine dysfunctions in relation to iron overload in multi transfused Indian thalassemia patients.

Authors:  Rashid H Merchant; Amruta Shirodkar; Javed Ahmed
Journal:  Indian J Pediatr       Date:  2011-01-14       Impact factor: 1.967

2.  Renal tubule function in beta-thalassemia after hematopoietic stem cell transplantation.

Authors:  Achra Sumboonnanonda; Kleebsabai Sanpakit; Nuntawan Piyaphanee
Journal:  Pediatr Nephrol       Date:  2008-08-08       Impact factor: 3.714

3.  Prevalence of beta-thalassemia trait in premarital screening in Al-Hassa, Saudi Arabia.

Authors:  Ahmad Al-Suliman
Journal:  Ann Saudi Med       Date:  2006 Jan-Feb       Impact factor: 1.526

4.  Study of serum haptoglobin level and its relation to erythropoietic activity in Beta thalassemia children.

Authors:  Seham M Ragab; Manal A Safan; Eman A Badr
Journal:  Mediterr J Hematol Infect Dis       Date:  2015-02-15       Impact factor: 2.576

5.  Fetal Hemoglobin Inducers from the Natural World: A Novel Approach for Identification of Drugs for the Treatment of {beta}-Thalassemia and Sickle-Cell Anemia.

Authors:  Nicoletta Bianchi; Cristina Zuccato; Ilaria Lampronti; Monica Borgatti; Roberto Gambari
Journal:  Evid Based Complement Alternat Med       Date:  2007-12-11       Impact factor: 2.629

6.  The Diagnostic Value of Pulsed Wave Tissue Doppler Imaging in Asymptomatic Beta- Thalassemia Major Children and Young Adults; Relation to Chemical Biomarkers of Left Ventricular Function and Iron Overload.

Authors:  Seham M Ragab; Waleed M Fathy; Walaa FAbd El-Aziz; Rasha T Helal
Journal:  Mediterr J Hematol Infect Dis       Date:  2015-08-24       Impact factor: 2.576

7.  Evaluation of Glutathione-S-Transferase P1 Polymorphism and its Relation to Bone Mineral Density in Egyptian Children and Adolescents with Beta-Thalassemia Major.

Authors:  Seham M Ragab; Eman A Badr; Ahmed S Ibrahim
Journal:  Mediterr J Hematol Infect Dis       Date:  2016-01-01       Impact factor: 2.576

8.  Nutritional biomarkers in children and adolescents with Beta-thalassemia-major: An Egyptian center experience.

Authors:  Laila M Sherief; Sanaa M Abd El-Salam; Naglaa M Kamal; Osama El Safy; Mohamed A A Almalky; Seham F Azab; Hemat M Morsy; Amal F Gharieb
Journal:  Biomed Res Int       Date:  2014-04-08       Impact factor: 3.411

  8 in total

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