Appropriatezza dei percorsi diagnostici per le emoglobinopatie: il caso Hb Hekinan
Author:
Publisher
Edizioni Minerva Medica
Subject
Biochemistry (medical),Medical Laboratory Technology
Link
http://link.springer.com/article/10.1007/s13631-018-0174-1/fulltext.html
Reference12 articles.
1. Angastiniotis M, Vives Corrons JL, Soteriades ES et al. (2013) The impact of migrations on the health services for rare diseases in Europe: the example of haemoglobin disorders. ScientificWorldJournal 2013:727905
2. A Database of Human Hemoglobin Variants and Thalassemias. http://globin.bx.psu.edu/hbvar/menu.html (Accesso 1 dicembre 2017)
3. Van Delft P, Lenters E, Bakker-Verweij M et al. (2009) Evaluating five dedicated automatic devices for hemoglobinopathy diagnostics in multi ethnic populations. Int J Lab Hematol 31:484–495
4. Traeger-Synodinos J, Harteveld CL, Old JM et al. (2015) EMQN Best Practice Guidelines for molecular and haematology methods for carrier identification and prenatal diagnosis of the haemoglobinopathies. Eur J Hum Genet 23:426–437
5. Ivaldi G, Barberio G (2012) Raccomandazioni per la Diagnostica di Primo Livello delle Emoglobinopatie della Società Italiana Talassemie ed Emoglobinopatie—SITE Collana scientifica SITE N 1
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