Citations (10)
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Ferania Mella, Yasuhiro Yamashiro, Chris Adhiyanto, Tatehiko Tanaka, Takenori Nitta, Yuki Amao & Masafumi Kimoto. (2018) A Coincidental Discovery of a New Stable Variant (Hb Hachioji or HBB: c.187C>T) in a Patient with Chronic Hemolytic Anemia of Unexplained Origin. Hemoglobin 42:1, pages 1-6.
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Margherita Vinciguerra, Cristina Passarello, Filippo Leto, Anna Crivello, Maria Fustaneo, Filippo Cassarà, Monica Cannata, Aurelio Maggio & Antonino Giambona. (2016) Coinheritance of a Rare Nucleotide Substitution on the β-Globin Gene and Other Known Mutations in the Globin Clusters: Management in Genetic Counseling. Hemoglobin 40:4, pages 231-235.
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Margherita Vinciguerra, Cristina Passarello, Filippo Cassarà, Filippo Leto, Monica Cannata, Anna Crivello, Veronica Di Salvo, Aurelio Maggio & Antonino Giambona. (2016) Hb San Cataldo [β144(HC1)Lys→Thr; HBB: C.434A > C]: A New Hemoglobin Variant with Increased Affinity for Oxygen. Hemoglobin 40:4, pages 223-227.
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Articles from other publishers (7)
Paloma Ropero, Jorge M. Nieto, Fernando-Ataúlfo González Fernández, Ana Villegas & Celina Benavente. (2021) Hb Maruchi [α165 (E14) Ala>Pro; HBA1: c.196G>C]: A new thalassemia hemoglobinopathy related to the alpha1 globin gene. Clinical Biochemistry 92, pages 77-81.
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M. Vinciguerra, C. Passarello, F. Cassarà, F. Leto, M. Cannata, G. Calvaruso, R. Di Maggio, D. Renda, A. Maggio & A. Giambona. (2016)
Co-heredity of silent CAP + 1570 T>C (
HBB
:c*96T>C) defect and severe β-thal mutation: a cause of mild β-thalassemia intermedia
. International Journal of Laboratory Hematology 38:1, pages 17-26.
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A. Giambona, G. Damiani, M. Vinciguerra, C. Jakil, M. Cannata, F. Cassarà, F. Picciotto, G. Schillaci, V. Cigna, D. Renda, F. Leto, C. Passarello & A. Maggio. (2015) Incidence of haemoglobinopathies in Sicily: the impact of screening and prenatal diagnosis. International Journal of Clinical Practice 69:10, pages 1129-1138.
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Margherita Vinciguerra, Cristina Passarello, Filippo Leto, Filippo Cassarà, Monica Cannata, Aurelio Maggio & Antonino Giambona. (2015) Co-inheritance of the rare β hemoglobin variants Hb Yaounde, Hb Görwihl and Hb City of Hope with other alterations in globin genes: impact in genetic counseling. European Journal of Haematology 94:4, pages 322-329.
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Margherita Vinciguerra, Cristina Passarello, Filippo Leto, Filippo Cassarà, Monica Cannata, Aurelio Maggio & Antonino Giambona. (2014)
Identification of three new nucleotide substitutions in the
β
-globin gene: laboratoristic approach and impact on genetic counselling for beta-thalassaemia
. European Journal of Haematology 92:5, pages 444-449.
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Antonino Giambona, Margherita Vinciguerra, Cristina Passarello, Maria A. La Rosa, Giuseppina Lo Giudice, Chiara Di Bella, Maria Amorini, Francesca Iacona, Carmelo Salpietro, Aurelio Maggio & Luciana Rigoli. (2010) Co‐inheritance of Hb Hershey [β70(E14) Ala→Gly] and Hb La Pommeraie [β133(H11)Val→Met] in a Sicilian subject. European Journal of Haematology 84:5, pages 453-457.
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Antonino Giambona, Cristina Passarello, Disma Renda & Aurelio Maggio. (2009) The significance of the hemoglobin A2 value in screening for hemoglobinopathies. Clinical Biochemistry 42:18, pages 1786-1796.
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