Giagu N - Search Results

1

Hyperbilirubinaemia in heterozygous beta-thalassaemia is related to co-inherited Gilbert's syndrome.

Galanello R, Perseu L, Melis MA, Cipollina L, Barella S, Giagu N, Turco MP, Maccioni O, Cao A. Galanello R, et al. Among authors: giagu n. Br J Haematol. 1997 Nov;99(2):433-6. doi: 10.1046/j.1365-2141.1997.3703182.x. Br J Haematol. 1997. PMID: 9375768 Free article.

2

Iron stores and iron deficiency anemia in children heterozygous for beta-thalassemia.

Galanello R, Turco MP, Barella S, Giagu N, Dessì C, Cornacchia G, Cao A. Galanello R, et al. Among authors: giagu n. Haematologica. 1990 Jul-Aug;75(4):319-22. Haematologica. 1990. PMID: 2276677

3

Co-inherited Gilbert's syndrome: a factor determining hyperbilirubinemia in homozygous beta-thalassemia.

Galanello R, Cipollina MD, Dessì C, Giagu N, Lai E, Cao A. Galanello R, et al. Among authors: giagu n. Haematologica. 1999 Feb;84(2):103-5. Haematologica. 1999. PMID: 10091405 Clinical Trial.

4

Association of α globin gene quadruplication and heterozygous β thalassemia in patients with thalassemia intermedia.

Sollaino MC, Paglietti ME, Perseu L, Giagu N, Loi D, Galanello R. Sollaino MC, et al. Among authors: giagu n. Haematologica. 2009 Oct;94(10):1445-8. doi: 10.3324/haematol.2009.005728. Haematologica. 2009. PMID: 19794088 Free PMC article.

5

HbH disease in Sardinia: molecular, hematological and clinical aspects.

Galanello R, Aru B, Dessì C, Addis M, Paglietti E, Melis MA, Cocco S, Massa P, Giagu N, Barella S, et al. Galanello R, et al. Among authors: giagu n. Acta Haematol. 1992;88(1):1-6. doi: 10.1159/000204585. Acta Haematol. 1992. PMID: 1414154

6

Molecular analysis of beta zero-thalassemia intermedia in Sardinia.

Galanello R, Dessi E, Melis MA, Addis M, Sanna MA, Rosatelli C, Argiolu F, Giagu N, Turco MP, Cacace E, et al. Galanello R, et al. Among authors: giagu n. Blood. 1989 Aug 1;74(2):823-7. Blood. 1989. PMID: 2473806 Free article.

7

Serum erythropoietin and erythropoiesis in high- and low-fetal hemoglobin beta-thalassemia intermedia patients.

Galanello R, Barella S, Turco MP, Giagu N, Cao A, Dore F, Liberato NL, Guarnone R, Barosi G. Galanello R, et al. Among authors: giagu n. Blood. 1994 Jan 15;83(2):561-5. Blood. 1994. PMID: 7506955 Free article.

8

Clinical and molecular analysis of haemoglobin H disease in Sardinia: haematological, obstetric and cardiac aspects in patients with different genotypes.

Origa R, Sollaino MC, Giagu N, Barella S, Campus S, Mandas C, Bina P, Perseu L, Galanello R. Origa R, et al. Among authors: giagu n. Br J Haematol. 2007 Jan;136(2):326-32. doi: 10.1111/j.1365-2141.2006.06423.x. Epub 2006 Nov 27. Br J Haematol. 2007. PMID: 17129226 Free 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: giagu n. 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

Delayed fetal hemoglobin switching in subjects with KLF1 gene mutation.

Satta S, Perseu L, Maccioni L, Giagu N, Galanello R. Satta S, et al. Among authors: giagu n. Blood Cells Mol Dis. 2012 Jan 15;48(1):22-4. doi: 10.1016/j.bcmd.2011.10.003. Epub 2011 Nov 16. Blood Cells Mol Dis. 2012. PMID: 22093801

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