Giordano PC - Search Results

1

Beta-thalassemia intermedia from southern Iran: IVS-II-1 (G-->A) is the prevalent thalassemia intermedia allele.

Karimi M, Yarmohammadi H, Farjadian S, Zeinali S, Moghaddam Z, Cappellini MD, Giordano PC. Karimi M, et al. Among authors: giordano pc. Hemoglobin. 2002 May;26(2):147-54. doi: 10.1081/hem-120005452. Hemoglobin. 2002. PMID: 12144057

2

Multi centric origin of Hb D-Punjab [beta121(GH4)Glu-->Gln, GAA>CAA].

Yavarian M, Karimi M, Paran F, Neven C, Harteveld CL, Giordano PC. Yavarian M, et al. Among authors: giordano pc. Hemoglobin. 2009;33(6):399-405. doi: 10.3109/03630260903344598. Hemoglobin. 2009. PMID: 19958184

3

Spectrum and haplotypes of the HFE hemochromatosis gene in Iran: H63D in beta-thalassemia major and the first E277K homozygous.

Karimi M, Yavarian M, Delbini P, Harteveld CL, Farjadian S, Fiorelli G, Giordano PC. Karimi M, et al. Among authors: giordano pc. Hematol J. 2004;5(6):524-7. doi: 10.1038/sj.thj.6200553. Hematol J. 2004. PMID: 15570296

4

Molecular basis of Hb H disease in southwest Iran.

Yavarian M, Karimi M, Zorai A, Harteveld CL, Giordano PC. Yavarian M, et al. Among authors: giordano pc. Hemoglobin. 2005;29(1):43-50. Hemoglobin. 2005. PMID: 15768554

5

Response to hydroxyurea treatment in Iranian transfusion-dependent beta-thalassemia patients.

Yavarian M, Karimi M, Bakker E, Harteveld CL, Giordano PC. Yavarian M, et al. Among authors: giordano pc. Haematologica. 2004 Oct;89(10):1172-8. Haematologica. 2004. PMID: 15477200 Clinical Trial.

6

Segmental duplications involving the alpha-globin gene cluster are causing beta-thalassemia intermedia phenotypes in beta-thalassemia heterozygous patients.

Harteveld CL, Refaldi C, Cassinerio E, Cappellini MD, Giordano PC. Harteveld CL, et al. Among authors: giordano pc. Blood Cells Mol Dis. 2008 May-Jun;40(3):312-6. doi: 10.1016/j.bcmd.2007.11.006. Epub 2008 Jan 14. Blood Cells Mol Dis. 2008. PMID: 18249014

7

Molecular spectrum of beta-thalassemia in the Iranian Province of Hormozgan.

Yavarian M, Harteveld CL, Batelaan D, Bernini LF, Giordano PC. Yavarian M, et al. Among authors: giordano pc. Hemoglobin. 2001 Feb;25(1):35-43. doi: 10.1081/hem-100103068. Hemoglobin. 2001. PMID: 11300348

8

Mosaic segmental uniparental isodisomy and progressive clonal selection: a common mechanism of late onset β-thalassemia major.

Harteveld CL, Refaldi C, Giambona A, Ruivenkamp CA, Hoffer MJ, Pijpe J, De Knijff P, Borgna-Pignatti C, Maggio A, Cappellini MD, Giordano PC. Harteveld CL, et al. Among authors: giordano pc. Haematologica. 2013 May;98(5):691-5. doi: 10.3324/haematol.2012.065219. Epub 2012 Sep 14. Haematologica. 2013. PMID: 22983591 Free PMC article.

9

Adult onset of a Thalassemia intermedia genotype in association with a -alpha-3.7 homozygosity. Hb G-Accra [beta73(e17)Asp-->Asn] in combination with beta- and alpha-thalassemia in the same family.

van der Padt A, Bouva M, Auwerda JJ, Dees A, Harteveld CL, Giordano PC. van der Padt A, et al. Among authors: giordano pc. Hemoglobin. 2005;29(4):269-76. doi: 10.1080/03630260500310554. Hemoglobin. 2005. PMID: 16370487

10

The rare codon 24 (T>A) (beta+) mutation in association with the common codon 39 (C> T) (beta0) mutation causes transfusion-dependent beta-thalassemia in a Moroccan patient.

Agouti I, Bennani M, Levy N, Giordano P, Badens C. Agouti I, et al. Hemoglobin. 2009;33(2):150-4. doi: 10.1080/03630260902861998. Hemoglobin. 2009. PMID: 19373592

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