National registry of hemoglobinopathies in Spain (REPHem)-Reference-Cited by-同舟云学术

National registry of hemoglobinopathies in Spain (REPHem)

Published:2016-11-02 Issue:7 Volume:64 Page:e26322
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatr Blood Cancer

Author:

Cela Elena¹²,Bellón José M.³,de la Cruz María³,Beléndez Cristina¹,Berrueco Rubén²,Ruiz Anna²,Elorza Izaskun²,Díaz de Heredia Cristina²,Cervera Aurea²,Vallés Griselda²,Salinas J. Antonio²,Coll M. Teresa²,Bermúdez Mar²,Prudencio Marta²,Argilés Bienvenida²,Vecilla Cruz²,

Affiliation:

1. Pediatric Hematology Unit; Hospital General Universitario Gregorio Marañón. Facultad de Medicina. Universidad Complutense de Madrid; Spain

2. Hemoglobinopathies Study Group- Sociedad Española de Hematología y Oncología Pediátricas-SEHOP; Spain

3. Instituto de Investigación Sanitaria Gregorio Marañón; Spain

Funder

Novartis España

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/pbc.26322/fullpdf

Reference39 articles.

1. A national register for surveillance of inherited disorders: beta thalassemia in the United Kingdom;Modell;Bull World Health Organ,2001

2. Sickle cell disease as a paradigm of immigration hematology: new challenges for hematologists in Europe;Roberts;Haematologica,2007

3. Global migration and the changing distribution of sickle haemoglobin: a quantitative study of temporal trends between 1960 and 2000;Piel;Lancet Global Health,2014

4. Global epidemiology of haemoglobin disorders and derived service indicators;Darlison;Bull World Health Organ,2008

5. Angastiniotis M Eleftheriou A Gulbis B Hemoglobinopathies on the move: is Europe ready? http://www.thalassaemia.org.cy/uploads/1450369075finalhaemoglobinopthiesonthemovereport2.pdf

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