National registry of hemoglobinopathies in Greece: updated demographics, current trends in affected births, and causes of mortality-Reference-Cited by-同舟云学术

National registry of hemoglobinopathies in Greece: updated demographics, current trends in affected births, and causes of mortality

Published:2018-09-08 Issue:1 Volume:98 Page:55-66
ISSN:0939-5555
Container-title:Annals of Hematology
language:en
Short-container-title:Ann Hematol

Author:

Voskaridou Ersi^ORCID, ,Kattamis Antonis,Fragodimitri Christina,Kourakli Alexandra,Chalkia Panagiota,Diamantidis Michael,Vlachaki Efthymia,Drosou Marouso,Lafioniatis Stilianos,Maragkos Konstantinos,Petropoulou Fotini,Eftihiadis Eftihios,Economou Marina,Klironomos Evangelos,Koutsouka Freideriki,Nestora Konstantina,Tzoumari Ioanna,Papageorgiou Ourania,Basileiadi Artemis,Lafiatis Ioannis,Dimitriadou Efthimia,Kalpaka Anastasia,Kalkana Chrysoula,Xanthopoulidis Georgios,Adamopoulos Ioannis,Kaiafas Panagiotis,Mpitzioni Aikaterini,Goula Anastasia,Kontonis Ioannis,Alepi Chrisoula,Anastasiadis Athanasios,Papadopoulou Margarita,Maili Polixeni,Dionisopoulou Dionisia,Tsirka Antigoni,Makis Alexandros,Kostaridou Stavroula,Politou Marianna,Papassotiriou Ioannis

Publisher

Springer Science and Business Media LLC

Subject

Hematology,General Medicine

Link

http://link.springer.com/article/10.1007/s00277-018-3493-4/fulltext.html

Reference44 articles.

1. Williams TN, Weatherall DJ (2012) World distribution, population genetics, and health burden of the hemoglobinopathies. Cold Spring Harb Perspect Med 2(9):a011692. https://doi.org/10.1101/cshperspect.a011692

2. Ladis V, Karagiorga-Lagana M, Tsatra I, Chouliaras G (2013) Thirty-year experience in preventing haemoglobinopathies in Greece: achievements and potentials for optimisation. Eur J Haematol 90(4):313–322. https://doi.org/10.1111/ejh.12076

3. Thompson AA, Walters MC, Kwiatkowski J, Rasko JEJ, Ribeil JA, Hongeng S, Magrin E, Schiller GJ, Payen E, Semeraro M, Moshous D, Lefrere F, Puy H, Bourget P, Magnani A, Caccavelli L, Diana JS, Suarez F, Monpoux F, Brousse V, Poirot C, Brouzes C, Meritet JF, Pondarre C, Beuzard Y, Chretien S, Lefebvre T, Teachey DT, Anurathapan U, Ho PJ, von Kalle C, Kletzel M, Vichinsky E, Soni S, Veres G, Negre O, Ross RW, Davidson D, Petrusich A, Sandler L, Asmal M, Hermine O, De Montalembert M, Hacein-Bey-Abina S, Blanche S, Leboulch P, Cavazzana M (2018) Gene therapy in patients with transfusion-dependent beta-thalassemia. N Engl J Med 378(16):1479–1493. https://doi.org/10.1056/NEJMoa1705342

4. Aguilar Martinez P, Angastiniotis M, Eleftheriou A, Gulbis B, Manu Pereira Mdel M, Petrova-Benedict R, Corrons JL (2014) Haemoglobinopathies in Europe: health & migration policy perspectives. Orphanet J Rare Dis 9:97. https://doi.org/10.1186/1750-1172-9-97

5. Voskaridou E, Ladis V, Kattamis A, Hassapopoulou E, Economou M, Kourakli A, Maragkos K, Kontogianni K, Lafioniatis S, Vrettou E, Koutsouka F, Papadakis A, Mihos A, Eftihiadis E, Farmaki K, Papageorgiou O, Tapaki G, Maili P, Theohari M, Drosou M, Kartasis Z, Aggelaki M, Basileiadi A, Adamopoulos I, Lafiatis I, Galanopoulos A, Xanthopoulidis G, Dimitriadou E, Mprimi A, Stamatopoulou M, Haile ED, Tsironi M, Anastasiadis A, Kalmanti M, Papadopoulou M, Panori E, Dimoxenou P, Tsirka A, Georgakopoulos D, Drandrakis P, Dionisopoulou D, Ntalamaga A, Davros I, Karagiorga M, Greek Haemoglobinopathies Study G (2012) A national registry of haemoglobinopathies in Greece: deducted demographics, trends in mortality and affected births. Ann Hematol 91(9):1451–1458. https://doi.org/10.1007/s00277-012-1465-7

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