|1.||Leto, Filippo: 1 article (04/2015)|
|2.||Vinciguerra, Margherita: 1 article (04/2015)|
|3.||Maggio, Aurelio: 1 article (04/2015)|
|4.||Cannata, Monica: 1 article (04/2015)|
|5.||Cassarà, Filippo: 1 article (04/2015)|
|6.||Passarello, Cristina: 1 article (04/2015)|
|7.||Giambona, Antonino: 1 article (04/2015)|
|8.||González, Neida: 1 article (09/2010)|
|9.||Arias, Sergio: 1 article (09/2010)|
|10.||Paradisi, Irene: 1 article (09/2010)|
|1.||beta-Thalassemia (Cooley's Anemia)
01/01/1989 - "This compound heterozygosity, observed for the first time in the Turkish population was characterized by a considerable increase in Hb F production, mainly of the G gamma type, as expected for a chromosome with haplotype IV. In the second family, the variant was Hb City of Hope [beta 69(E13)Gly----Ser] which was present in combination with an unknown type of beta-thalassemia. "
01/01/1989 - "Beta-thalassemia intermedia in two Turkish families is caused by the interaction of Hb Knossos [beta 27(B9)Ala----Ser] and of Hb City of Hope [beta 69(E13)Gly----ser] with beta (0)-thalassemia."
04/01/2015 - "This work allowed us to describe the co-inheritance of three rare β hemoglobin variants with other alterations in globin genes: the β hemoglobin variant Hb Yaounde [β134(H12)Val>Ala], found for the first time in combination with ααα(anti3.7) arrangement, and the β hemoglobin variants Hb Görwihl [β5(A2)Pro>Ala] and Hb City of Hope [β69(E13)Gly>Ser], found both in association with β(0) -thalassemia. "