Giordano PC - Search Results

1

Towards a prevention program for β-thalassemia. The molecular spectrum in East Java, Indonesia.

Hernanda PY, Tursilowati L, Arkesteijn SG, Ugrasena ID, Larasati MC, Soeatmadji SM, Giordano PC, Harteveld CL. Hernanda PY, et al. Among authors: giordano pc. Hemoglobin. 2012;36(1):1-6. doi: 10.3109/03630269.2011.642914. Epub 2011 Dec 21. Hemoglobin. 2012. PMID: 22188014

2

A confidential inquiry estimating the number of patients affected with sickle cell disease and thalassemia major confirms the need for a prevention strategy in the Netherlands.

Giordano PC, Bouva MJ, Harteveld CL. Giordano PC, et al. Hemoglobin. 2004;28(4):287-96. doi: 10.1081/hem-200037735. Hemoglobin. 2004. PMID: 15658185

3

Ggamma -37 (A-->T): a new nondeletional hereditary persistence of fetal hemoglobin determinant associated with the rare codon 91 (+T) delta0-thalassemia.

Bouva MJ, Harteveld CL, Bakker-Verweij G, van Delft P, Giordano PC. Bouva MJ, et al. Among authors: giordano pc. Hemoglobin. 2006;30(3):371-7. doi: 10.1080/03630260600755641. Hemoglobin. 2006. PMID: 16840228

4

Hb Lepore-Leiden: a new delta/beta rearrangement associated with a beta-thalassemia minor phenotype.

Harteveld CL, Wijermans PW, Arkesteijn SG, Van Delft P, Kerkhoffs JL, Giordano PC. Harteveld CL, et al. Among authors: giordano pc. Hemoglobin. 2008;32(5):446-53. doi: 10.1080/03630260802173429. Hemoglobin. 2008. PMID: 18932069

5

Frequency of alpha-globin gene triplications and their interaction with beta-thalassemia mutations.

Giordano PC, Bakker-Verwij M, Harteveld CL. Giordano PC, et al. Hemoglobin. 2009;33(2):124-31. doi: 10.1080/03630260902827684. Hemoglobin. 2009. PMID: 19373588

6

Two new alpha1-globin gene point mutations: Hb Nedlands (HBA1:c.86C>T) [alpha28(B9)Ala-->Val] and Hb Queens Park (HBA1:c.98T>A) [alpha32(B13)Met-->Lys].

Phylipsen M, Prior JF, Lim E, Lingam N, Finlayson J, Arkesteijn SG, Harteveld CL, Giordano PC. Phylipsen M, et al. Among authors: giordano pc. Hemoglobin. 2010 Jan;34(2):123-6. doi: 10.3109/03630261003679854. Hemoglobin. 2010. PMID: 20353346

7

Extended molecular spectrum of beta- and alpha-thalassemia in Oman.

Hassan SM, Hamza N, Jaffer Al-Lawatiya F, Jaffer Mohammed A, Harteveld CL, Rajab A, Giordano PC. Hassan SM, et al. Among authors: giordano pc. Hemoglobin. 2010 Jan;34(2):127-34. doi: 10.3109/03630261003673147. Hemoglobin. 2010. PMID: 20353347

8

New and known β-thalassemia determinants masked by known and new δ gene defects [Hb A(2)-Ramallah or δ6(A3)Glu→Gln, GAG>>CAG].

Phylipsen M, Harteveld CL, de Metz M, Gallivan MV, Arkesteijn SG, Luo HY, Chui DH, Giordano PC. Phylipsen M, et al. Among authors: giordano pc. Hemoglobin. 2010;34(5):445-50. doi: 10.3109/03630269.2010.511591. Hemoglobin. 2010. PMID: 20854118

9

Molecular spectrum of α-globin gene defects in the Omani population.

Hassan SM, Harteveld CL, Bakker E, Giordano PC. Hassan SM, et al. Among authors: giordano pc. Hemoglobin. 2014;38(6):422-6. doi: 10.3109/03630269.2014.976414. Epub 2014 Nov 5. Hemoglobin. 2014. PMID: 25370869

10

Broader spectrum of β-thalassemia mutations in Oman: regional distribution and comparison with neighboring countries.

Hassan SM, Harteveld CL, Bakker E, Giordano PC. Hassan SM, et al. Among authors: giordano pc. Hemoglobin. 2015;39(2):107-10. doi: 10.3109/03630269.2015.1009632. Epub 2015 Feb 13. Hemoglobin. 2015. PMID: 25677748

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