Giambona A - Search Results

1

Rasburicase-induced Methemoglobinemia: A Case Report and Literature Review.

Pirrone I, Farruggia P, Cacciatore F, Giambona A, Guarina A, Marcello AP, Mosa C, Scalzo S, D'Angelo P. Pirrone I, et al. Among authors: giambona a. J Pediatr Hematol Oncol. 2021 Aug 1;43(6):e886-e890. doi: 10.1097/MPH.0000000000001979. J Pediatr Hematol Oncol. 2021. PMID: 33122582 Review.

2

Early prenatal diagnosis of Hb Lepore Boston-Washington and β-thalassemia on fetal celomatic DNA.

Giambona A, Leto F, Cassarà F, Tartaglia V, Marchese G, Orlandi E, Cigna V, Picciotto F, Maggio A, Vinciguerra M. Giambona A, et al. Int J Lab Hematol. 2022 Aug;44(4):796-802. doi: 10.1111/ijlh.13837. Epub 2022 Mar 25. Int J Lab Hematol. 2022. PMID: 35333433

3

Early prenatal diagnosis of hemoglobinopathies by celocentesis is ready for use in routine clinical practice.

Giambona A, Leto F, Cassarà F, Tartaglia V, Marchese G, Orlandi E, Cigna V, Picciotto F, Maggio A, Vinciguerra M. Giambona A, et al. Int J Lab Hematol. 2023 Feb;45(1):e19-e20. doi: 10.1111/ijlh.13961. Epub 2022 Sep 4. Int J Lab Hematol. 2023. PMID: 36059154 No abstract available.

4

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: giambona a. 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

5

Embryo-fetal erythroid cell selection from celomic fluid allows earlier prenatal diagnosis of hemoglobinopathies.

Giambona A, Damiani G, Leto F, Jakil C, Renda D, Cigna V, Schillaci G, Picciotto F, Nicolaides KH, Passarello C, Makrydimas G, Maggio A. Giambona A, et al. Prenat Diagn. 2016 Apr;36(4):375-81. doi: 10.1002/pd.4793. Epub 2016 Mar 29. Prenat Diagn. 2016. PMID: 26891446

6

Coheredity of a new silent mutation: c.-29G>T, with a severe β-thal mutation in a patient with β-thalassemia intermediate.

Vinciguerra M, Passarello C, Cassarà F, Leto F, Cannata M, Calvaruso G, Renda D, Maggio A, Giambona A. Vinciguerra M, et al. Among authors: giambona a. Int J Lab Hematol. 2018 Apr;40(2):e17-e20. doi: 10.1111/ijlh.12777. Epub 2018 Feb 5. Int J Lab Hematol. 2018. PMID: 29405650 No abstract available.

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: giambona a. Hemoglobin. 2016 Aug;40(4):223-7. doi: 10.1080/03630269.2016.1182550. Epub 2016 Jun 2. Hemoglobin. 2016. PMID: 27250824

8

Evaluation of the BeTha gene 1 kit for the qualitative detection of the eight most common Mediterranean beta-thalassemia mutations.

Ugozzoli LA, Lowery JD, Reyes AA, Lin CI, Re A, Locati F, Galanello R, Macioni L, Maggio A, Giambona A, Loutradi A, Boussiou M, Wallace RB. Ugozzoli LA, et al. Among authors: giambona a. Am J Hematol. 1998 Nov;59(3):214-22. doi: 10.1002/(sici)1096-8652(199811)59:3<214::aid-ajh6>3.0.co;2-z. Am J Hematol. 1998. PMID: 9798659 Free article.

9

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

10

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. 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

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