Vinciguerra M - Search Results

1

Celomic Fluid: Laboratory Workflow for Prenatal Diagnosis of Monogenic Diseases.

Giambona A, Vinciguerra M, Leto F, Cassarà F, Tartaglia V, Cigna V, Orlandi E, Picciotto F, Al Qahtani NH, Alsulmi ES, Almandil NB, AbdulAzeez S, Borgio JF, Maggio A. Giambona A, et al. Among authors: vinciguerra m. Mol Diagn Ther. 2022 Mar;26(2):239-252. doi: 10.1007/s40291-022-00577-3. Epub 2022 Feb 17. Mol Diagn Ther. 2022. PMID: 35175567

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: vinciguerra m. Hemoglobin. 2006;30(2):139-48. doi: 10.1080/03630260600642005. Hemoglobin. 2006. PMID: 16798637

3

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: vinciguerra m. Haematologica. 2008 Sep;93(9):1380-4. doi: 10.3324/haematol.12840. Epub 2008 Jul 4. Haematologica. 2008. PMID: 18603555 Free article.

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: vinciguerra m. 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

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: vinciguerra m. 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

6

Iron deficiency does not compromise the diagnosis of high HbA(2) β thalassemia trait.

Passarello C, Giambona A, Cannata M, Vinciguerra M, Renda D, Maggio A. Passarello C, et al. Among authors: vinciguerra m. Haematologica. 2012 Mar;97(3):472-3. doi: 10.3324/haematol.2011.052357. Epub 2011 Nov 18. Haematologica. 2012. PMID: 22102712 Free PMC article. No abstract available.

7

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. Eur J Haematol. 2014;92(5):444-9. doi: 10.1111/ejh.12267. Epub 2014 Mar 15. Eur J Haematol. 2014. PMID: 24401016

8

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. Eur J Haematol. 2015 Apr;94(4):322-9. doi: 10.1111/ejh.12431. Epub 2014 Dec 22. Eur J Haematol. 2015. PMID: 25113778

9

Incidence of haemoglobinopathies in Sicily: the impact of screening and prenatal diagnosis.

Giambona A, Damiani G, Vinciguerra M, Jakil C, Cannata M, Cassarà F, Picciotto F, Schillaci G, Cigna V, Renda D, Leto F, Passarello C, Maggio A. Giambona A, et al. Among authors: vinciguerra m. Int J Clin Pract. 2015 Oct;69(10):1129-38. doi: 10.1111/ijcp.12628. Epub 2015 Feb 27. Int J Clin Pract. 2015. PMID: 25727926

10

Phenotypic evaluations of -223 T>C (HBB:c.-223T>C) nucleotide substitution in the promoter region of β-globin gene.

Giambona A, Passarello C, Cassarà F, Cannata M, Leto F, Vinciguerra M. Giambona A, et al. Among authors: vinciguerra m. Blood Cells Mol Dis. 2015 Oct;55(3):218-9. doi: 10.1016/j.bcmd.2015.06.006. Epub 2015 Jun 26. Blood Cells Mol Dis. 2015. PMID: 26227850 No abstract available.

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