Galanello R - Search Results

1

A mutation in the TMPRSS6 gene, encoding a transmembrane serine protease that suppresses hepcidin production, in familial iron deficiency anemia refractory to oral iron.

Melis MA, Cau M, Congiu R, Sole G, Barella S, Cao A, Westerman M, Cazzola M, Galanello R. Melis MA, et al. Among authors: galanello r. Haematologica. 2008 Oct;93(10):1473-9. doi: 10.3324/haematol.13342. Epub 2008 Jul 4. Haematologica. 2008. PMID: 18603562 Free article.

2

H63D mutation in the HFE gene increases iron overload in beta-thalassemia carriers.

Melis MA, Cau M, Deidda F, Barella S, Cao A, Galanello R. Melis MA, et al. Among authors: galanello r. Haematologica. 2002 Mar;87(3):242-5. Haematologica. 2002. PMID: 11869934

3

Iron-deficiency anemia secondary to mutations in genes controlling hepcidin.

Cau M, Melis MA, Congiu R, Galanello R. Cau M, et al. Among authors: galanello r. Expert Rev Hematol. 2010 Apr;3(2):205-16. doi: 10.1586/ehm.10.2. Expert Rev Hematol. 2010. PMID: 21083463 Review.

4

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

Cau M, Galanello R, Giagu N, Melis MA. Cau M, et al. Among authors: galanello r. Blood Cells Mol Dis. 2012 Feb 15;48(2):121-3. doi: 10.1016/j.bcmd.2011.11.007. Epub 2011 Dec 14. Blood Cells Mol Dis. 2012. PMID: 22169218

5

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. Haematologica. 1990 Jul-Aug;75(4):319-22. Haematologica. 1990. PMID: 2276677

6

Frequency of hemochromatosis C282Y and H63D mutations in Sardinia.

Melis MA, Cau M, Congiu R, Ruvoletto L, Cao A, Galanello R. Melis MA, et al. Among authors: galanello r. Genet Test. 2002 Winter;6(4):327-9. doi: 10.1089/10906570260471886. Genet Test. 2002. PMID: 12537659

7

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. Among authors: galanello r. Haematologica. 2011 May;96(5):767-70. doi: 10.3324/haematol.2010.037333. Epub 2011 Jan 27. Haematologica. 2011. PMID: 21273267 Free PMC article.

8

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. Origa R, et al. Among authors: galanello r. Haematologica. 2015 May;100(5):e169-71. doi: 10.3324/haematol.2014.115733. Epub 2015 Jan 16. Haematologica. 2015. PMID: 25596269 Free PMC article. No abstract available.

9

Hemoglobin Sabine [beta 91 (F7) Leu-->Pro]: occurrence in a Sardinian individual with hemolytic anemia and inclusion bodies.

Gasperini D, Galanello R, Melis MA, Iannelli S, Giordano P, Bernini LF, Cao A. Gasperini D, et al. Among authors: galanello r. Haematologica. 1992 Sep-Oct;77(5):381-3. Haematologica. 1992. PMID: 1336469

10

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. Acta Haematol. 1992;88(1):1-6. doi: 10.1159/000204585. Acta Haematol. 1992. PMID: 1414154

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