Leto F - Search Results

1

Fetal aneuploidy diagnosed at celocentesis for early prenatal diagnosis of congenital hemoglobinopathies.

Giambona A, Leto F, Passarello C, Vinciguerra M, Cigna V, Schillaci G, Picciotto F, Lauricella S, Nicolaides KH, Makrydimas G, Damiani G, Maggio A. Giambona A, et al. Among authors: leto f. Acta Obstet Gynecol Scand. 2018 Mar;97(3):312-321. doi: 10.1111/aogs.13287. Epub 2018 Jan 24. Acta Obstet Gynecol Scand. 2018. PMID: 29292496 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: leto f. Hemoglobin. 2006;30(2):139-48. doi: 10.1080/03630260600642005. Hemoglobin. 2006. PMID: 16798637

3

External quality assessment of hemoglobin A2 measurement: data from an Italian pilot study with fresh whole blood samples and commercial HPLC systems.

Paleari R, Giambona A, Cannata M, Leto F, Maggio A, Mosca A; IFCC Working Group Standardization of HbA2. Paleari R, et al. Among authors: leto f. Clin Chem Lab Med. 2007;45(1):88-92. doi: 10.1515/CCLM.2007.002. Clin Chem Lab Med. 2007. PMID: 17243922

4

Embryo-fetal erythroid megaloblasts in the human coelomic cavity.

Renda MC, Giambona A, Fecarotta E, Leto F, Makrydimas G, Renda D, Damiani G, Jakil MC, Picciotto F, Piazza A, Valtieri M, Maggio A. Renda MC, et al. Among authors: leto f. J Cell Physiol. 2010 Nov;225(2):385-9. doi: 10.1002/jcp.22269. J Cell Physiol. 2010. PMID: 20533375

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: leto f. 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

Feasibility of DNA diagnosis of haemoglobinopathies on coelocentesis.

Giambona A, Makrydimas G, Leto F, Damiani G, Jakil MC, Picciotto F, Renda D, Fiorino R, Renda MC, Schillaci G, Gueli-Alletti D, Nicolaides KH, Maggio A. Giambona A, et al. Among authors: leto f. Br J Haematol. 2011 Apr;153(2):268-72. doi: 10.1111/j.1365-2141.2011.08621.x. Epub 2011 Mar 8. Br J Haematol. 2011. PMID: 21385172 Free article.

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. Among authors: leto f. 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. Among authors: leto f. 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: leto f. 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: leto f. 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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