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Results: 1-13 |
Results: 13
Different geographic origins of Hb constant spring [alpha(2) codon 142 TAA-> CAA]
Authors: Harteveld, CL Traeger-Synodinos, J Ragusa, A Fichera, M Kanavakis, E Kattamis, C Giordano, P Schiliro, G Bernini, LF
Citation: Cl. Harteveld et al., Different geographic origins of Hb constant spring [alpha(2) codon 142 TAA-> CAA], HAEMATOLOG, 86(1), 2001, pp. 36-38
Molecular spectrum of beta-thalassemia in the Iranian province of hormozgan
Authors: Yavarian, M Harteveld, CL Batelaan, D Bernini, LF Giordano, PC
Citation: M. Yavarian et al., Molecular spectrum of beta-thalassemia in the Iranian province of hormozgan, HEMOGLOBIN, 25(1), 2001, pp. 35-43
Very mild pathology in a case of Hb S/beta(0)-thalassemia in combination with a homozygosity for the alpha-thalassemia 3.7 kb deletion
Authors: Kerkhoffs, JL Harteveld, CL Wijermans, P van Delft, P Haak, HL Bernini, LF Giordano, PC
Citation: Jl. Kerkhoffs et al., Very mild pathology in a case of Hb S/beta(0)-thalassemia in combination with a homozygosity for the alpha-thalassemia 3.7 kb deletion, HEMOGLOBIN, 24(3), 2000, pp. 259-263
Letter to the editor and authors' response: Chromatographic measurements of hemoglobin A(2) in blood samples containing sickle hemoglobin
Authors: Giordano, PC Harteveld, CL
Citation: Pc. Giordano et Cl. Harteveld, Letter to the editor and authors' response: Chromatographic measurements of hemoglobin A(2) in blood samples containing sickle hemoglobin, ANN CLIN L, 30(4), 2000, pp. 430-430
alpha-Thalassaemia as a result of a novel splice donor site mutation of the alpha(1)-globin gene
Authors: Harteveld, CL Beijer, C van Delft, P Zanardini, R Bernini, LF Giordano, PC
Citation: Cl. Harteveld et al., alpha-Thalassaemia as a result of a novel splice donor site mutation of the alpha(1)-globin gene, BR J HAEM, 110(3), 2000, pp. 694-698
A complex haemoglobinopathy diagnosis in a family with both beta(0)- and alpha(0/+)-thalassaemia homozygosity
Authors: Giordano, PC Harteveld, CL Bok, LA van Delft, P Batelaan, D Beemer, FA Bernini, LF
Citation: Pc. Giordano et al., A complex haemoglobinopathy diagnosis in a family with both beta(0)- and alpha(0/+)-thalassaemia homozygosity, EUR J HUM G, 7(2), 1999, pp. 163-168
Hb Aghia Sophia [alpha 62(E11)Val -> 0 (alpha 1)], an "in-frame" deletion causing alpha-thalassemia
Authors: Traeger-Synodinos, J Harteveld, CL Kanavakis, E Giordano, PC Kattamis, C Bernini, LF
Citation: J. Traeger-synodinos et al., Hb Aghia Sophia [alpha 62(E11)Val -> 0 (alpha 1)], an "in-frame" deletion causing alpha-thalassemia, HEMOGLOBIN, 23(4), 1999, pp. 317-324
The second case of dominant beta-thalassemia induced by the codon 127 (CAG-> TAG) described as a De Novo mutation in a Dutch boy
Authors: Van Weel, M Harteveld, CL Bernini, LF Brouwers, TM Giordano, PC
Citation: M. Van Weel et al., The second case of dominant beta-thalassemia induced by the codon 127 (CAG-> TAG) described as a De Novo mutation in a Dutch boy, HEMOGLOBIN, 23(4), 1999, pp. 389-393
Hb Nijkerk: a new mutation at codons 138/139 of the beta-globin gene inducing severe hemolytic anemia in a Dutch girl
Authors: van den Berg, HM Bruin, MCA Batelaan, D van Delft, P van Zwieten, R Roos, D Harteveld, CL Bernini, LF Giordano, PC
Citation: Hm. Van Den Berg et al., Hb Nijkerk: a new mutation at codons 138/139 of the beta-globin gene inducing severe hemolytic anemia in a Dutch girl, HEMOGLOBIN, 23(2), 1999, pp. 135-144
Haplotype analysis of two new, independent cases of Hb Osu-Christiansborg
Authors: Giordano, PC Harteveld, CL Bernini, LF Doorduijn, JK Geenen, AA Kok, PJM Versteegh, FGA
Citation: Pc. Giordano et al., Haplotype analysis of two new, independent cases of Hb Osu-Christiansborg, HEMOGLOBIN, 23(2), 1999, pp. 193-195
Haemoglobinopathy analyses in the Netherlands: a report of an in vitro globin chain biosynthesis survey using a rapid, modified method
Authors: Giordano, PC Van Delft, P Batelaan, D Harteveld, CL Bernini, LF
Citation: Pc. Giordano et al., Haemoglobinopathy analyses in the Netherlands: a report of an in vitro globin chain biosynthesis survey using a rapid, modified method, CLIN LAB H, 21(4), 1999, pp. 247-255
alpha-thalassaemia
Authors: Bernini, LF Harteveld, CL
Citation: Lf. Bernini et Cl. Harteveld, alpha-thalassaemia, BAIL CLIN H, 11(1), 1998, pp. 53-90
Phenotype variability of the dominant beta-thalassemia induced in four Dutch families by the rare cd121 (G -> T) mutation
Authors: Giordano, PC Harteveld, CL Michiels, JJ Terpstra, W Schelfhout, LJDM Appel, IM Batelaan, D van Delft, P Plug, RJ Bernini, LF
Citation: Pc. Giordano et al., Phenotype variability of the dominant beta-thalassemia induced in four Dutch families by the rare cd121 (G -> T) mutation, ANN HEMATOL, 77(6), 1998, pp. 249-255
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