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Does Profile of Hemoglobin Eβ-thalassemia Patients Change After Splenectomy? Experience of a Tertiary Thalassemia Care Centre in Eastern India

Hemoglobin Eβ-thalassemia is by far the commonest form of thalassemia intermedia. Its phenotype ranges from mild anemia to severe transfusion-dependency necessitating splenectomy in many patients. The present study aimed to systematically analyze both clinical as well as laboratory parameters in pro...

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Detalhes bibliográficos
Publicado no:Indian J Hematol Blood Transfus
Main Authors: Mandal, Prakas Kumar, Ghosh, Malay Kumar, Bhattacharyya, Maitreyee
Formato: Artigo
Idioma:Inglês
Publicado em: Springer India 2015
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4542765/
https://ncbi.nlm.nih.gov/pubmed/26306069
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12288-014-0498-6
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