Cargando…
Immigration and screening programs for hemoglobinopathies in Italy, Spain and Turkey
Sickle cell disease (SCD) and thalassemias are the most common monogenic diseases in the world. The number of migrants and refugees in Europe and Turkey, in the past decade, has increased dramatically due to war, violence or prosecutions in their homeland. Prevention and management of haemoglobin di...
Autores principales: | Canatan, Duran, Vives Corrons, Joan Lluis, Piacentini, Giorgio, Kara, Fatih, Keskinkılıç, Bekir, Tezel, Başak, Külekçi Uğur, Aslıhan, Babayiğit, Meliha, Krishnevskaya, Elena, Millimaggi, Giuseppe, Erinekçi, Ozlem, Özdemir, Zekiye, de Sanctis, Vincenzo |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Mattioli 1885
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8477095/ https://www.ncbi.nlm.nih.gov/pubmed/34487057 http://dx.doi.org/10.23750/abm.v92i4.11965 |
Ejemplares similares
-
Foreword - Advances in Hemoglobinopathies: A new section of Acta Biomedica
por: de Sanctis, Vincenzo
Publicado: (2021) -
Blood transfusion and iron overload in patients with Sickle Cell Disease (SCD): Personal experience and a short update of diabetes mellitus occurrence
por: Soliman, Ashraf T, et al.
Publicado: (2022) -
A Short Review on Growth and Endocrine Long-term Complications in Children and Adolescents with β-Thalassemia Major: Conventional Treatment versus Hematopoietic Stem Cell Transplantation
por: Ahmed, Shayma, et al.
Publicado: (2022) -
The Effects of Treatment with Blood Transfusion, Iron Chelation and Hydroxyurea on Puberty, Growth and Spermatogenesis in Sickle Cell Disease (SCD): A short update
por: Soliman, Ashraf T, et al.
Publicado: (2021) -
The different patterns of insulin response during oral glucose tolerance test (OGTT) in transfused young patients with β-thalassemia
por: Kattamis, Christos, et al.
Publicado: (2021)