Renda D - Search Results

1

Clinical and hematological responses to hydroxyurea in Sicilian patients with Hb S/beta-thalassemia.

Rigano P, Rodgers GP, Renda D, Renda MC, Aquino A, Maggio A. Rigano P, et al. Among authors: renda d, renda mc. Hemoglobin. 2001 Feb;25(1):9-17. doi: 10.1081/hem-100103065. Hemoglobin. 2001. PMID: 11300353 Clinical Trial.

2

Chronic Administration of Hydroxyurea (HU) Benefits Caucasian Patients with Sickle-Beta Thalassemia.

Di Maggio R, Hsieh MM, Zhao X, Calvaruso G, Rigano P, Renda D, Tisdale JF, Maggio A. Di Maggio R, et al. Among authors: renda d. Int J Mol Sci. 2018 Feb 28;19(3):681. doi: 10.3390/ijms19030681. Int J Mol Sci. 2018. PMID: 29495591 Free PMC article.

3

Clinical and hematological response to hydroxyurea in a patient with Hb Lepore/beta-thalassemia.

Rigano P, Manfré L, La Galla R, Renda D, Renda MC, Calabrese A, Calzolari R, Maggio A. Rigano P, et al. Among authors: renda d, renda mc. Hemoglobin. 1997 May;21(3):219-26. doi: 10.3109/03630269708997382. Hemoglobin. 1997. PMID: 9140718

4

Desensitization to hydroxycarbamide following long-term treatment of thalassaemia intermedia as observed in vivo and in primary erythroid cultures from treated patients.

Rigano P, Pecoraro A, Calzolari R, Troia A, Acuto S, Renda D, Pantalone GR, Maggio A, Di Marzo R. Rigano P, et al. Among authors: renda d. Br J Haematol. 2010 Dec;151(5):509-15. doi: 10.1111/j.1365-2141.2010.08397.x. Epub 2010 Oct 19. Br J Haematol. 2010. PMID: 20955403 Free article. Clinical Trial.

5

Deferiprone versus deferoxamine in sickle cell disease: results from a 5-year long-term Italian multi-center randomized clinical trial.

Calvaruso G, Vitrano A, Di Maggio R, Ballas S, Steinberg MH, Rigano P, Sacco M, Telfer P, Renda D, Barone R, Maggio A; Investigators of the Multicenter Randomized Clinical Trial of Deferiprone versus Deferoxamine in Sickle-Cell-Disease. Calvaruso G, et al. Among authors: renda d. Blood Cells Mol Dis. 2014 Dec;53(4):265-71. doi: 10.1016/j.bcmd.2014.04.004. Epub 2014 May 9. Blood Cells Mol Dis. 2014. PMID: 24814618 Clinical Trial.

6

HBB: c.316-125A>G and HBB: c.316-42delC: Phenotypic Evaluations of Two Rare Changes in the Second Intron of the HBB Gene.

Vinciguerra M, Cannata M, Cassarà F, Passarello C, Leto F, Calvaruso G, Renda D, Maggio A, Giambona A. Vinciguerra M, et al. Among authors: renda d. Hemoglobin. 2017 Jul-Nov;41(4-6):234-238. doi: 10.1080/03630269.2017.1397014. Epub 2017 Nov 24. Hemoglobin. 2017. PMID: 29171316

7

Oral supplements of vitamin E improve measures of oxidative stress in plasma and reduce oxidative damage to LDL and erythrocytes in beta-thalassemia intermedia patients.

Tesoriere L, D'Arpa D, Butera D, Allegra M, Renda D, Maggio A, Bongiorno A, Livrea MA. Tesoriere L, et al. Among authors: renda d, d arpa d. Free Radic Res. 2001 May;34(5):529-40. doi: 10.1080/10715760100300461. Free Radic Res. 2001. PMID: 11378535 Clinical Trial.

8

Cardiac complications in thalassemia: noninvasive detection methods and new directions in the clinical management.

Mancuso L, Panzarella G, Bartolotta TV, Midiri M, Renda D, Maggio A. Mancuso L, et al. Among authors: renda d. Expert Rev Cardiovasc Ther. 2003 Sep;1(3):439-52. doi: 10.1586/14779072.1.3.439. Expert Rev Cardiovasc Ther. 2003. PMID: 15030271 Review.

9

Analysis of delta-globin gene alleles in the Sicilian population: identification of five new mutations.

Giambona A, Passarello C, Ruggeri G, Renda D, Teresi P, Anzà M, Maggio A. Giambona A, et al. Among authors: renda d. Haematologica. 2006 Dec;91(12):1681-4. Haematologica. 2006. PMID: 17145605

10

Hb Southern Italy: coexistence of two missence mutations (the Hb Sun Prairie alpha2 130 Ala --> Pro and Hb Caserta alpha2 26 Ala --> Thr) in a single HBA2 gene.

Passarello C, Giambona A, Prossomariti L, Ammirabile M, Pucci P, Renda D, Pagano L, Maggio A. Passarello C, et al. Among authors: renda d. Br J Haematol. 2008 Oct;143(1):138-42. doi: 10.1111/j.1365-2141.2008.07319.x. Epub 2008 Aug 4. Br J Haematol. 2008. PMID: 18691171 Free article.

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