Passarello C - Search Results

1

Hb Southern Italy: coexistence of two missence mutations (the Hb Sun Prairie alpha2 130 Ala --> Pro and Hb Caserta alpha2 26 Ala --> Thr) in a single HBA2 gene.

Passarello C, Giambona A, Prossomariti L, Ammirabile M, Pucci P, Renda D, Pagano L, Maggio A. Passarello C, et al. Br J Haematol. 2008 Oct;143(1):138-42. doi: 10.1111/j.1365-2141.2008.07319.x. Epub 2008 Aug 4. Br J Haematol. 2008. PMID: 18691171 Free article.

2

Hb Marineo [beta70(E14)Ala-->Val]: a silent hemoglobin variant with a mutation within the heme pocket.

Giambona A, Vinciguerra M, Cassarà F, Li Muli R, Leto F, Passarello C, Wajcman H, Maggio A. Giambona A, et al. Among authors: passarello c. Hemoglobin. 2006;30(2):139-48. doi: 10.1080/03630260600642005. Hemoglobin. 2006. PMID: 16798637

3

Analysis of delta-globin gene alleles in the Sicilian population: identification of five new mutations.

Giambona A, Passarello C, Ruggeri G, Renda D, Teresi P, Anzà M, Maggio A. Giambona A, et al. Among authors: passarello c. Haematologica. 2006 Dec;91(12):1681-4. Haematologica. 2006. PMID: 17145605

4

Co-inheritance of Hb Hershey [beta70(E14) Ala-->Gly] and Hb La Pommeraie [beta133(H11)Val-->Met] in a Sicilian subject.

Giambona A, Vinciguerra M, Passarello C, La Rosa MA, Lo Giudice G, Di Bella C, Amorini M, Iacona F, Salpietro C, Maggio A, Rigoli L. Giambona A, et al. Among authors: passarello c. Eur J Haematol. 2010 May;84(5):453-7. doi: 10.1111/j.1600-0609.2010.01414.x. Epub 2010 Jan 5. Eur J Haematol. 2010. PMID: 20059533

5

Identification of three new nucleotide substitutions in the β-globin gene: laboratoristic approach and impact on genetic counselling for beta-thalassaemia.

Vinciguerra M, Passarello C, Leto F, Cassarà F, Cannata M, Maggio A, Giambona A. Vinciguerra M, et al. Among authors: passarello c. Eur J Haematol. 2014;92(5):444-9. doi: 10.1111/ejh.12267. Epub 2014 Mar 15. Eur J Haematol. 2014. PMID: 24401016

6

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.

Vinciguerra M, Passarello C, Leto F, Cassarà F, Cannata M, Maggio A, Giambona A. Vinciguerra M, et al. Among authors: passarello c. Eur J Haematol. 2015 Apr;94(4):322-9. doi: 10.1111/ejh.12431. Epub 2014 Dec 22. Eur J Haematol. 2015. PMID: 25113778

7

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.

Vinciguerra M, Passarello C, Cassarà F, Leto F, Cannata M, Calvaruso G, Di Maggio R, Renda D, Maggio A, Giambona A. Vinciguerra M, et al. Among authors: passarello c. Int J Lab Hematol. 2016 Feb;38(1):17-26. doi: 10.1111/ijlh.12433. Epub 2015 Sep 29. Int J Lab Hematol. 2016. PMID: 26418075

8

Significance of borderline hemoglobin A2 values in an Italian population with a high prevalence of beta-thalassemia.

Giambona A, Passarello C, Vinciguerra M, Li Muli R, Teresi P, Anzà M, Ruggeri G, Renda D, Maggio A. Giambona A, et al. Among authors: passarello c. Haematologica. 2008 Sep;93(9):1380-4. doi: 10.3324/haematol.12840. Epub 2008 Jul 4. Haematologica. 2008. PMID: 18603555 Free article.

9

The significance of the hemoglobin A(2) value in screening for hemoglobinopathies.

Giambona A, Passarello C, Renda D, Maggio A. Giambona A, et al. Among authors: passarello c. Clin Biochem. 2009 Dec;42(18):1786-96. doi: 10.1016/j.clinbiochem.2009.06.026. Epub 2009 Jul 8. Clin Biochem. 2009. PMID: 19591816 Review.

10

The genetic heterogeneity of β-globin gene defects in Sicily reflects the historic population migrations of the island.

Giambona A, Vinciguerra M, Cannata M, Cassarà F, Fiorentino G, Leto F, Gioco PL, Renda D, Passarello C, Maggio A. Giambona A, et al. Among authors: passarello c. Blood Cells Mol Dis. 2011 Apr 15;46(4):282-7. doi: 10.1016/j.bcmd.2011.01.006. Epub 2011 Feb 24. Blood Cells Mol Dis. 2011. PMID: 21353607

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