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Endocrine profile of β-thalassemia major patients followed from childhood to advanced adulthood in a tertiary care center

Aim: Chronic iron overload resulting from frequent transfusions, poor compliance to efficient chelation therapy and chronic liver disease is basically responsible for the most severe complications of thalassemia major (TM). Before conventional treatment, TM was entirely childhood disease with a very...

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Detalhes bibliográficos
Main Authors: Vincenzo De Sanctis, Heba Elsedfy, Ashraf T Soliman, Ihab Zaki Elhakim, Nada A Soliman, Rania Elalaily, Christos Kattamis
Formato: Artigo
Idioma:Inglês
Publicado em: Wolters Kluwer Medknow Publications 2016-01-01
Colecção:Indian Journal of Endocrinology and Metabolism
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Acesso em linha:http://www.ijem.in/article.asp?issn=2230-8210;year=2016;volume=20;issue=4;spage=451;epage=459;aulast=De
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