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Thalidomide in Patients with Transfusion-Dependent E-Beta Thalassemia Refractory to Hydroxyurea: A Single-Center Experience

Transfusion-dependent E-Beta (EB) thalassemia is one of the major causes of hereditary hemoglobinopathies in India. Hydroxyurea has been tried for HbF induction and amelioration of the transfusion frequency in EB thalassemia. The primary objective of this retrospective study, conducted between Janua...

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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Indian J Hematol Blood Transfus
Prif Awduron: Nag, Arijit, Radhakrishnan, Vivek S., Kumar, Jeevan, Bhave, Saurabh, Mishra, Deepak Kumar, Nair, Reena, Chandy, Mammen
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Springer India 2020
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC7229140/
https://ncbi.nlm.nih.gov/pubmed/32425398
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12288-020-01263-2
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