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Items: 17

1.

Differences in the erythropoiesis-hepcidin-iron store axis between hemoglobin H disease and β-thalassemia intermedia.

Origa R, Cazzola M, Mereu E, Danjou F, Barella S, Giagu N, Galanello R, Swinkels DW.

Haematologica. 2015 May;100(5):e169-71. doi: 10.3324/haematol.2014.115733. Epub 2015 Jan 16. No abstract available.

2.

A decisional algorithm to start iron chelation in patients with beta thalassemia.

Danjou F, Cabantchik ZI, Origa R, Moi P, Marcias M, Barella S, Defraia E, Dessì C, Foschini ML, Giagu N, Leoni GB, Morittu M, Galanello R.

Haematologica. 2014 Mar;99(3):e38-40. doi: 10.3324/haematol.2013.098202. No abstract available.

3.

Responsiveness to oral iron and ascorbic acid in a patient with IRIDA.

Cau M, Galanello R, Giagu N, Melis MA.

Blood Cells Mol Dis. 2012 Feb 15;48(2):121-3. doi: 10.1016/j.bcmd.2011.11.007. Epub 2011 Dec 14.

PMID:
22169218
4.

Delayed fetal hemoglobin switching in subjects with KLF1 gene mutation.

Satta S, Perseu L, Maccioni L, Giagu N, Galanello R.

Blood Cells Mol Dis. 2012 Jan 15;48(1):22-4. doi: 10.1016/j.bcmd.2011.10.003. Epub 2011 Nov 16.

PMID:
22093801
5.

Red cell pyruvate kinase deficiency in Southern Sardinia.

Perseu L, Giagu N, Satta S, Sollaino MC, Congiu R, Galanello R.

Blood Cells Mol Dis. 2010 Dec 15;45(4):280-3. doi: 10.1016/j.bcmd.2010.08.006. Epub 2010 Sep 25.

PMID:
20870434
6.

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.

Haematologica. 2009 Oct;94(10):1445-8. doi: 10.3324/haematol.2009.005728.

7.

Liver iron concentrations and urinary hepcidin in beta-thalassemia.

Origa R, Galanello R, Ganz T, Giagu N, Maccioni L, Faa G, Nemeth E.

Haematologica. 2007 May;92(5):583-8.

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.

Br J Haematol. 2007 Jan;136(2):326-32. Epub 2006 Nov 27.

PMID:
17129226
9.

[Histological picture of liver disease in thalassemia intermedia].

Mancosu MG, Galanello R, Ambu R, De Virgiliis S, Giagu N, Cao A, Faa G.

Pathologica. 2000 Aug;92(4):241-8. Italian.

PMID:
11029884
10.

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.

Haematologica. 1999 Feb;84(2):103-5.

11.

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.

Br J Haematol. 1997 Nov;99(2):433-6.

PMID:
9375768
12.

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.

Blood. 1994 Jan 15;83(2):561-5.

PMID:
7506955
13.

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.

Acta Haematol. 1992;88(1):1-6.

PMID:
1414154
14.

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.

Haematologica. 1990 Jul-Aug;75(4):319-22.

PMID:
2276677
15.

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.

Blood. 1989 Aug 1;74(2):823-7.

PMID:
2473806
16.

Hematological phenotype of carriers of deletion alpha-thalassemia according to the alpha-globin genotype.

Galanello R, Paglietti E, Giagu N, Melis MA, Scalas MT, Cao A.

Haematologica. 1985 May-Jun;70(3):191-8. No abstract available.

PMID:
3932145
17.

Molecular mechanism accounting for milder types of thalassemia major.

Furbetta M, Tuveri T, Rosatelli C, Angius A, Falchi AM, Cossu P, Meloni A, Giagu N, Cao A.

J Pediatr. 1983 Jul;103(1):35-9.

PMID:
6191017

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