HbS/β+ thalassemia: Really a mild disease? A National survey from the AIEOP Sickle Cell Disease Study Group with genotype‐phenotype correlation-Reference-Cited by-同舟云学术

HbS/β+ thalassemia: Really a mild disease? A National survey from the AIEOP Sickle Cell Disease Study Group with genotype‐phenotype correlation

Published:2019-12-12 Issue:3 Volume:104 Page:214-222
ISSN:0902-4441
Container-title:European Journal of Haematology
language:en
Short-container-title:Eur J Haematol

Author:

Notarangelo Lucia Dora¹,Agostini Annalisa²,Casale Maddalena³^ORCID,Samperi Piera⁴,Arcioni Francesco⁵,Gorello Paolo⁶,Perrotta Silverio³^ORCID,Masera Nicoletta⁷,Barone Angelica⁸,Bertoni Elisa¹,Bonetti Elisa⁹,Burnelli Roberta¹⁰,Casini Tommaso¹¹,Del Vecchio Giovanni Carlo¹²,Filippini Beatrice¹³,Giona Fiorina¹⁴^ORCID,Giordano Paola¹²^ORCID,Gorio Chiara¹,Marchina Eleonora¹⁵,Nardi Margherita¹⁶,Petrone Angela¹⁷,Colombatti Raffaella¹⁸^ORCID,Sainati Laura¹⁸,Russo Giovanna⁴^ORCID

Affiliation:

1. Hematology Oncology Unit Children's Hospital ASST Spedali Civili Brescia Italy

2. Pediatrics Clinic University of Brescia Spedali Civili di Brescia Brescia Italy

3. Department of Woman, Child and General and Specialist Surgery Università degli Studi della Campania "Luigi Vanvitelli" Napoli Italy

4. Unit of Pediatric Hematology and Oncology Department of Clinical and Experimental Medicine University of Catania Catania Italy

5. Pediatric Hematology and Oncology with Bone Marrow Transplation Azienda Ospedaliera di Perugia Perugia Italy

6. Department of Medicine University of Perugia CREO Hematology Perugia Italy

7. Department of Pediatrics Università di Milano Bicocca Fondazione MBBM Monza Italy

8. Department of Pediatric Onco‐Hematology Azienda Ospedaliero‐Universitaria di Parma Parma Italy

9. Department of Pediatric Onco‐Hematology Azienda Ospedaliera Universitaria Integrata Verona Italy

10. Pediatric Oncology University Hospital Sant'Anna Hospital Ferrara Italy

11. Pediatric Hematology‐Oncology IRCCS Meyer Children's Hospital Florence Italy

12. Pediatric Unit "F. Vecchio" Department of Biomedical Sciences and Human Oncology University of Bari "Aldo Moro" Bari Italy

13. Department of Pediatrics Infermi Hospital Rimini Rimini Italy

14. Department of Cellular Biotechnologies and Hematology Policlinico Umberto I Sapienza University Hematology Rome Italy

15. Division of Biology and Genetics Department of Molecular and Translational Medicine University of Brescia Brescia Italy

16. Onco‐Hematologic Pediatric Center University Hospital of Pisa Pisa Italy

17. Department of Pediatrics Rovereto Hospital Rovereto Italy

18. Clinic of Pediatric Hematology Oncology Department of Woman's and Child Health Azienda Ospedaliera‐Università di Padova Padova Italy

Publisher

Wiley

Subject

Hematology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/ejh.13362

Reference51 articles.

1. Classification of the Disorders of Hemoglobin

2. Organizing national responses for rare blood disorders: the Italian experience with sickle cell disease in childhood

3. Newborn screening for sickle cell disease in Europe: recommendations from a Pan-European Consensus Conference

4. Hb S-β-Thalassemia: Molecular, Hematological and Clinical Comparisons

5. Minireview: Clinical severity in sickle cell disease: the challenges of definition and prognostication

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