Satta S - Search Results

1

IFNL3 polymorphisms and HCV infection in patients with beta thalassemia.

Origa R, Marceddu G, Danjou F, Perseu L, Satta S, Demartis FR, Piga A, Longo F, Lai ME, Vacquer S, Galanello R. Origa R, et al. Among authors: satta s. Ann Hepatol. 2015 May-Jun;14(3):389-95. Ann Hepatol. 2015. PMID: 25864220 Free article.

2

Hb Sassari [alpha 126(H9)Asp-->His] results from a GAC-->CAC mutation in the alpha 1-globin gene.

Paglietti E, Barella S, Satta S, Perra C, Cao A, Galanello R. Paglietti E, et al. Among authors: satta s. Hemoglobin. 1998 Jan;22(1):65-7. doi: 10.3109/03630269809071518. Hemoglobin. 1998. PMID: 9494049 No abstract available.

3

Globin chain synthesis analysis by high performance liquid chromatography in the screening of thalassemia syndromes.

Galanello R, Satta S, Pirroni MG, Travi M, Maccioni L. Galanello R, et al. Among authors: satta s. Hemoglobin. 1998 Sep-Nov;22(5-6):501-8. doi: 10.3109/03630269809071547. Hemoglobin. 1998. PMID: 9859933

4

Homozygosity for nondeletion delta-beta(0) thalassemia resulting in a silent clinical phenotype.

Galanello R, Barella S, Satta S, Maccioni L, Pintor C, Cao A. Galanello R, et al. Among authors: satta s. Blood. 2002 Sep 1;100(5):1913-4. Blood. 2002. PMID: 12176917 Free article.

5

Hb Belfast [beta15(A12)Trp-->Arg]: definition of the clinical and hematological phenotype.

Galanello R, Perseu L, Barella S, Satta S, Fais A, Era B, Corda M. Galanello R, et al. Among authors: satta s. Hemoglobin. 2004 Aug;28(3):217-22. doi: 10.1081/hem-120040219. Hemoglobin. 2004. PMID: 15481889

6

Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia.

Uda M, Galanello R, Sanna S, Lettre G, Sankaran VG, Chen W, Usala G, Busonero F, Maschio A, Albai G, Piras MG, Sestu N, Lai S, Dei M, Mulas A, Crisponi L, Naitza S, Asunis I, Deiana M, Nagaraja R, Perseu L, Satta S, Cipollina MD, Sollaino C, Moi P, Hirschhorn JN, Orkin SH, Abecasis GR, Schlessinger D, Cao A. Uda M, et al. Among authors: satta s. Proc Natl Acad Sci U S A. 2008 Feb 5;105(5):1620-5. doi: 10.1073/pnas.0711566105. Epub 2008 Feb 1. Proc Natl Acad Sci U S A. 2008. PMID: 18245381 Free PMC article.

7

Glutathione S-transferase gene polymorphism and cardiac iron overload in thalassaemia major.

Origa R, Satta S, Matta G, Galanello R. Origa R, et al. Among authors: satta s. Br J Haematol. 2008 Jul;142(1):143-5. doi: 10.1111/j.1365-2141.2008.07175.x. Epub 2008 May 8. Br J Haematol. 2008. PMID: 18477036 Free article. No abstract available.

8

Amelioration of Sardinian beta0 thalassemia by genetic modifiers.

Galanello R, Sanna S, Perseu L, Sollaino MC, Satta S, Lai ME, Barella S, Uda M, Usala G, Abecasis GR, Cao A. Galanello R, et al. Among authors: satta s. Blood. 2009 Oct 29;114(18):3935-7. doi: 10.1182/blood-2009-04-217901. Epub 2009 Aug 20. Blood. 2009. PMID: 19696200 Free PMC article.

9

Red cell pyruvate kinase deficiency in Southern Sardinia.

Perseu L, Giagu N, Satta S, Sollaino MC, Congiu R, Galanello R. Perseu L, et al. Among authors: satta s. Blood Cells Mol Dis. 2010 Dec 15;45(4):280-3. doi: 10.1016/j.bcmd.2010.08.006. Epub 2010 Sep 25. Blood Cells Mol Dis. 2010. PMID: 20870434

10

Compound heterozygosity for KLF1 mutations associated with remarkable increase of fetal hemoglobin and red cell protoporphyrin.

Satta S, Perseu L, Moi P, Asunis I, Cabriolu A, Maccioni L, Demartis FR, Manunza L, Cao A, Galanello R. Satta S, et al. Haematologica. 2011 May;96(5):767-70. doi: 10.3324/haematol.2010.037333. Epub 2011 Jan 27. Haematologica. 2011. PMID: 21273267 Free PMC article.

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