A complication risk score to evaluate clinical severity of thalassaemia syndromes-Reference-Cited by-同舟云学术

A complication risk score to evaluate clinical severity of thalassaemia syndromes

Published:2020-11-20 Issue:3 Volume:192 Page:626-633
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:Br J Haematol

Author:

Vitrano Angela¹^ORCID,Meloni Antonella²^ORCID,Addario Pollina Walter³,Karimi Mehran⁴^ORCID,El‐Beshlawy Amal⁵,Hajipour Mahmoud⁶,Di Marco Vito⁷,Hussain Ansari Saqib⁸,Filosa Aldo⁹,Ricchi Paolo⁹^ORCID,Ceci Adriana¹⁰,Daar Shahina¹¹¹²,Titi Singer Sylvia¹³,Naserullah Zaki A.¹⁴,Pepe Alessia²,Scondotto Salvatore³,Dardanoni Gabriella³,Bonifazi Fedele¹⁰,Vichinsky Elliott¹³,Maggio Aurelio¹

Affiliation:

1. Campus of Haematology Franco and Piera Cutino AOOR Villa Sofia‐V. Cervello PalermoItaly

2. U.O.C. MRIFondazione Toscana G. Monasterio PisaItaly

3. D.A.S.O.ERegione Siciliana PalermoItaly

4. Haematology Research CenterShiraz University of Medical Sciences Shiraz Iran

5. Cairo University Giza Egypt

6. Department of Epidemiology School of Public Health and Safety Shahid Beheshti University of Medical Sciences Tehran Iran

7. Sezione di Gastroenterologia e Epatologia Dipartimento Biomedico di Medicina Interna e Specialistica University of Palermo Palermo Italy

8. Department of Paediatric Haematology and Molecular Medicine National Institute of Blood Diseases and Bone Marrow Transplantation Karachi Pakistan

9. Rare Blood Cell Disease Unit, "Cardarelli" Hospital NaplesItaly

10. Fondazione per la Ricerca Farmacologica Gianni Benzi Onlus Valenzano BA Italy

11. Department of Haematology College of Medicine and Health Sciences Sultan Qaboos University Muscat Sultanate of Oman

12. Wallenberg Research Centre Stellenbosch Institute for Advanced StudyStellenbosch University Stellenbosch South Africa

13. Haematology/Oncology Department Oakland CA USA

14. Dammam Maternity and Child Hospital Dammam Saudi Arabia

Publisher

Wiley

Subject

Hematology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/bjh.17203

Reference31 articles.

1. The genetic heterogeneity of β-globin gene defects in Sicily reflects the historic population migrations of the island

2. The Molecular Basis of -Thalassemia

3. Global epidemiology of haemoglobin disorders and derived service indicators

4. Thalassaemia

5. The inherited diseases of hemoglobin are an emerging global health burden

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