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Coexistence of Genetic Diseases Is a New Clinical Challenge: Three Unrelated Cases of Dual Diagnosis.
Genes (Basel). 2023 Feb 14;14(2):484. doi: 10.3390/genes14020484.
Genes (Basel). 2023.
PMID: 36833411
Free PMC article.
Genotoxic effect of iron overload and disease complications in transfused β thalassaemic patients.
Ferro E, Visalli G, La Rosa MA, Piraino B, Civa R, Randazzo Papa G, Di Pietro A.
Ferro E, et al. Among authors: civa r.
Mutagenesis. 2017 Mar 1;32(2):275-281. doi: 10.1093/mutage/gew062.
Mutagenesis. 2017.
PMID: 27932515
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Oxidative damage and genotoxicity biomarkers in transfused and untransfused thalassemic subjects.
Ferro E, Visalli G, Civa R, La Rosa MA, Randazzo Papa G, Baluce B, D'Ascola DG, Piraino B, Salpietro C, Di Pietro A.
Ferro E, et al. Among authors: civa r.
Free Radic Biol Med. 2012 Nov 15;53(10):1829-37. doi: 10.1016/j.freeradbiomed.2012.08.592. Epub 2012 Sep 6.
Free Radic Biol Med. 2012.
PMID: 22995637
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The role of anaemia in oxidative and genotoxic damage in transfused β-thalassaemic patients.
Ferro E, Visalli G, La Rosa MA, Civa R, Papa GR, D'Ascola DG, Roccamo G, Piraino B, Salpietro C, Di Pietro A.
Ferro E, et al. Among authors: civa r.
Hematology. 2017 Apr;22(3):183-191. doi: 10.1080/10245332.2016.1244034. Epub 2016 Nov 1.
Hematology. 2017.
PMID: 27801288
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Fibroscan: a new noninvasive method for evaluation of liver dysfunction in Turner syndrome.
Messina MF, Squadrito G, Valenzise M, Maimone S, Iannelli S, Arrigo T, Cacciola I, Civa R, D'agata V, Raimondo G, De Luca F.
Messina MF, et al. Among authors: civa r.
Eur J Clin Invest. 2011 Feb;41(2):183-8. doi: 10.1111/j.1365-2362.2010.02397.x. Epub 2010 Oct 21.
Eur J Clin Invest. 2011.
PMID: 20964679
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Neurocognitive profile in Turner's syndrome is not affected by growth impairment.
Messina MF, Zirilli G, Civa R, Rulli I, Salzano G, Aversa T, Valenzise M.
Messina MF, et al. Among authors: civa r.
J Pediatr Endocrinol Metab. 2007 Jun;20(6):677-84. doi: 10.1515/jpem.2007.20.6.677.
J Pediatr Endocrinol Metab. 2007.
PMID: 17663292
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Unbalanced segregation of a complex four-break 5q23-31 insertion in the 5p13 band in a malformed child.
Giardino D, Finelli P, Amico FP, Gottardi G, Civa R, Corona G, Nocera G, Larizza L.
Giardino D, et al. Among authors: civa r.
Eur J Hum Genet. 2004 Jun;12(6):455-9. doi: 10.1038/sj.ejhg.5201150.
Eur J Hum Genet. 2004.
PMID: 15054394
Review.
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