Recent Publications on Beta-Thalassemia: |  |
A genome-wide association identified the common genetic variants influence disease severity in beta(0)-thalassemia/hemoglobin E.
beta-Thalassemia/HbE disease is clinically variable. In searching for...
Direct Link | 20th November, 2009
| Thalassemia Research Center, Institute of Molecular Biosciences, Mahidol
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alpha-Thalassaemia Masked by beta Gene Defects and a New Polyadenylation Site Mutation on the alpha2-Globin Gene.
ABSTRACT We report three examples of chronic anaemia involving complex...
Direct Link | 17th November, 2009
| The Reference Hemoglobinopathies Laboratory, Department of Human and
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Deferasirox (Exjade) for the treatment of iron overload.
Deferasirox is a once-daily oral iron chelator with established...
Direct Link | 13th November, 2009
| Fondazione Ospedale Maggiore Policlinico, Istituto di Ricovero e Cura a
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The range of hemoglobin A(2) in hemoglobin E heterozygotes as determined by capillary electrophoresis.
Capillary electrophoresis (CE) is capable of distinguishing hemoglobin E...
Direct Link | 13th November, 2009
| Department of Pathology, St Joseph Mercy Hospital, Ann Arbor, MI 48106,
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Pregnancy and {beta}-thalassemia: an Italian multicenter experience.
Background Recent advances on the management of thalassemia have...
Direct Link | 12th November, 2009
| ASL Cagliari, Dipartimento di Scienze Biomediche e Biotecnologie,
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Improvement in oxidative stress and antioxidant parameters in beta-thalassemia/Hb E patients treated with curcuminoids.
OBJECTIVES: To evaluate the hematological profile, oxidative stress, and...
Direct Link | 11th November, 2009
| Department of Biochemistry, Faculty of Medicine Siriraj Hospital, Mahidol
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| Update on the use of deferasirox in the management of iron overload.
| 10th November, 2009
| American University of Beirut, Beirut, Lebanon;
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| [Beta-thalassemia major: French situation]
| 10th November, 2009
| Laboratoire de genetique moleculaire, Hopital d'enfants de La timone,
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| [THE FUNCTIONAL STATE OF LIVER IN PATIENTS WITH MAJOR beta-THALASSEMIA.]
| 7th November, 2009
| Azerbaijan State Training Institute for Physicians named after A. Aliyev,
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Cardiac mortality in {beta}-thalassemia major: resting but not dobutamine stress echocardiography predicts mortality among initially cardiac disease-free patients in a prospective 12-year study.
The current research was conducted to study the functional state of liver...
Direct Link | 6th November, 2009
| Department of Cardiology, Patras University Medical School, 7 Larnakos
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Escalating doses of donor lymphocytes for incipient graft rejection following SCT for thalassemia.
Mixed chimerism (MC) and secondary graft failure are frequent events...
Direct Link | 3rd November, 2009
| Pediatric Immunohematology and Bone Marrow Transplantation Unit, San
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| Clinical strategies for supporting the untransfusable hemorrhaging patient.
| 30th October, 2009
| Department of Oncology (Melmed, Holmes) and the Department of Pathology
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Assessing the Potential Success of Cystic Fibrosis Carrier Screening: Lessons Learned from Tay-Sachs Disease and beta-Thalassemia.
Objective: The objective of this study was to identify factors involved in...
Direct Link | 30th October, 2009
| Institute for Public Health Genetics, University of Washington, Seattle,
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| Case Study: using a continuous glucose monitoring system in a patient with diabetes and beta-thalassemia hemoglobinopathy.
| 30th October, 2009
| Department of Medicine, College of Medicine, Sultan Qaboos University,
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pHCR: a Parallel Haplotype Configuration Reduction algorithm for haplotype interaction analysis.
Finding gene interaction models is one of the most important issues in...
Direct Link | 30th April, 2008
| [1] Department of Biochemistry, Faculty of Medicine Siriraj Hospital,
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