Cannata M - Search Results

1

Analytical evaluation of the Tosoh HLC-723 G7 automated HPLC analyzer for hemoglobin A2 and F determination.

Paleari R, Cannata M, Leto F, Maggio A, Demartis FR, Desogus MF, Galanello R, Mosca A. Paleari R, et al. Among authors: cannata m. Clin Biochem. 2005 Feb;38(2):159-65. doi: 10.1016/j.clinbiochem.2004.10.017. Clin Biochem. 2005. PMID: 15642279

2

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: cannata m. Clin Chem Lab Med. 2007;45(1):88-92. doi: 10.1515/CCLM.2007.002. Clin Chem Lab Med. 2007. PMID: 17243922

3

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

4

Coinheritance of a Rare Nucleotide Substitution on the β-Globin Gene and Other Known Mutations in the Globin Clusters: Management in Genetic Counseling.

Vinciguerra M, Passarello C, Leto F, Crivello A, Fustaneo M, Cassarà F, Cannata M, Maggio A, Giambona A. Vinciguerra M, et al. Among authors: cannata m. Hemoglobin. 2016 Aug;40(4):231-5. doi: 10.1080/03630269.2016.1188400. Epub 2016 Jun 3. Hemoglobin. 2016. PMID: 27258795

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: cannata 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

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

7

Hb San Cataldo [β144(HC1)Lys→Thr; HBB: C.434A > C]: A New Hemoglobin Variant with Increased Affinity for Oxygen.

Vinciguerra M, Passarello C, Cassarà F, Leto F, Cannata M, Crivello A, Di Salvo V, Maggio A, Giambona A. Vinciguerra M, et al. Among authors: cannata m. Hemoglobin. 2016 Aug;40(4):223-7. doi: 10.1080/03630269.2016.1182550. Epub 2016 Jun 2. Hemoglobin. 2016. PMID: 27250824

8

Phenotypic evaluations of HBB:c.93-23T>C, a nucleotide substitution in the IVS I nt 108 of β-globin gene.

Vinciguerra M, Cassarà F, Cannata M, Renda D, Calvaruso G, Leto F, Passarello C, Maggio A, Giambona A. Vinciguerra M, et al. Among authors: cannata m. J Clin Pathol. 2017 Aug 9:jclinpath-2017-204651. doi: 10.1136/jclinpath-2017-204651. Online ahead of print. J Clin Pathol. 2017. PMID: 28794124

9

Phenotypic Evaluation of a Novel Nucleotide Substitution (HBD: c.442T>C) on the δ-Globin Gene.

Cassarà F, Vinciguerra M, Cannata M, Marchese G, Passarello C, Leto F, Maggio A, Giambona A. Cassarà F, et al. Among authors: cannata m. Hemoglobin. 2017 May;41(3):220-222. doi: 10.1080/03630269.2017.1371036. Hemoglobin. 2017. PMID: 28840768

10

Co-inheritance of HBB:c.-106G > C, a rare single nucleotide variation at position -56 relative to transcription initiation site, with other known mutations in the globin clusters.

Vinciguerra M, Passarello C, Cassarà F, Leto F, Cannata M, Ferro E, Anzà D, Calvaruso G, Maggio A, Giambona A. Vinciguerra M, et al. Among authors: cannata m. Hematology. 2018 Jul;23(6):368-372. doi: 10.1080/10245332.2017.1403737. Epub 2017 Nov 20. Hematology. 2018. PMID: 29157184 Free article.

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