Thalassemia-free and graft-versus-host-free survival: outcomes of hematopoietic stem cell transplantation for thalassemia major, Turkish experience

MA Yesilipek, V Uygun, A Kupesiz, G Karasu… - Bone Marrow …, 2022 - nature.com
We report the national data on the outcomes of hematopoietic stem cell transplantation
(HSCT) for thalassemia major (TM) patients in Turkey on behalf of the Turkish Pediatric Stem …

Life expectancy and risk factors for early death in patients with severe thalassemia syndromes in South India

R Dhanya, A Sedai, K Ankita, L Parmar… - Blood …, 2020 - ashpublications.org
In spite of advances in chelation therapy and screening of blood, mortality associated with
the most common life-threatening noncommunicable disease of children in India, transfusion …

[HTML][HTML] Hematopoietic stem cell transplantation in thalassemia patients: a Jordanian single centre experience

M Mustafa, M Qatawneh, M Al Jazazi, O Jarrah… - Materia Socio …, 2020 - ncbi.nlm.nih.gov
Aim: To evaluate the outcome of children who underwent allogenic hematopoietic stem Cell
transplantation as a curative approach for Thalassemia Major, treated at Queen Rania AL …

[HTML][HTML] The DKMS-BMST Thalassemia program: Description, scope and impact

N Agarwal, K Jothi, S Gambhir, G Rall… - Pediatric Hematology …, 2023 - Elsevier
Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is the only established
curative therapy for thalassemia. However, access to transplantation is constrained in limited …

[PDF][PDF] Economic burden of beta-thalassaemia major receiving hypertransfusion therapy at a public hospital in Mumbai.

A Uchil, M Muranjan, NJ Gogtay - National Medical Journal of India, 2023 - nmji.in
Background. Treating beta-thalassaemia major may entail high costs with considerable out-
of-pocket expenditure. Therefore, determination and valuation of the economic costs of a …

The polymorphism of HLA class I and II alleles in Indian patient with thalassemia

VC Mishra, D Chandra, A Raina, R Sharma, V Raina… - Human Gene, 2023 - Elsevier
Numerous HLA allele relations with various diseases have been observed all over the
world, including leukemia, aplastic anemia, and thalassemia. The current study looked at the …

Spectrum of Thalassemia and Hemoglobinopathy Using Capillary Zone Electrophoresis: A Facility-Based Single Centred Study at icddr, b in Bangladesh

A Hasan, J Ahmed, BC Chanda, M Aniqua… - Thalassemia …, 2023 - mdpi.com
Background: Although the global thalassemia zone covers Bangladesh, there are very
limited studies conducted in this region. Therefore, the focus of our study is to understand …

[HTML][HTML] How to setup a successful transplant program for hemoglobinopathies in developing countries: the Cure2Children approach

L Faulkner - Hematology/Oncology and Stem Cell Therapy, 2020 - Elsevier
Hematopoietic stem cell transplantation (HSCT) remains the only established definitive cure
for severe hemoglobinopathies, such as sickle cell disease (SCD) and thalassemia—the …

[HTML][HTML] New cost-effective human leukocyte antigen testing algorithm for screening of human leukocyte antigen-matched related donor in thalassemia major patient …

P Singh, AK Tiwari, VC Mishra, D Chandra… - Indian Journal of …, 2023 - journals.lww.com
Results: The new sequential HLA-A, HLA-B, and HLA-DRB1 testing algorithm showed a
49.1% reduction in cost compared to the conventional HLA testing algorithm. Furthermore …

Haematopoietic Stem Cell Transplantation in a Government Setup in India: New Directions in Indian Healthcare; Way to Go!

T Chatterjee, R Bhargava, S More, P Mehta, S Rai… - papers.ssrn.com
Introduction: Haematopoietic stem cell transplant (HSCT) is indicated for several disorders
as potentially curative treatment. However, establishing SCT unit demands infrastructure …