Harteveld CL - Search Results

1

Prevention of Thalassaemias and Other Haemoglobin Disorders: Volume 1: Principles [Internet].

Angastiniotis M, Eleftheriou A, Galanello R, Harteveld CL, Petrou M, Traeger-Synodinos J, Giordano P, Jauniaux E, Modell B, Serour G, authors. Old J, editor. Angastiniotis M, et al. Among authors: harteveld cl. 2nd edition. Nicosia (Cyprus): Thalassaemia International Federation; 2013. 2nd edition. Nicosia (Cyprus): Thalassaemia International Federation; 2013. PMID: 24672827 Free Books & Documents. Review.

2

Homozygous beta+ thalassaemia owing to a mutation in the cleavage-polyadenylation sequence of the human beta globin gene.

Losekoot M, Fodde R, Harteveld CL, van Heeren H, Giordano PC, Went LN, Bernini LF. Losekoot M, et al. Among authors: harteveld cl. J Med Genet. 1991 Apr;28(4):252-5. doi: 10.1136/jmg.28.4.252. J Med Genet. 1991. PMID: 1856830 Free PMC article.

3

Prenatal diagnosis of homozygous alpha zero-thalassemia by an immunological method.

Bernini LF, Kanhai HH, Losekoot M, Giordano P, Harteveld CL. Bernini LF, et al. Among authors: harteveld cl. Ann N Y Acad Sci. 1994 Sep 7;731:193-6. doi: 10.1111/j.1749-6632.1994.tb55769.x. Ann N Y Acad Sci. 1994. PMID: 7944118 No abstract available.

4

A novel polyadenylation signal mutation in the alpha 2-globin gene causing alpha thalassaemia.

Harteveld CL, Losekoot M, Haak H, Heister GA, Giordano PC, Bernini LF. Harteveld CL, et al. Br J Haematol. 1994 May;87(1):139-43. doi: 10.1111/j.1365-2141.1994.tb04883.x. Br J Haematol. 1994. PMID: 7947237

5

A case of non-beta-globin gene linked beta thalassaemia in a Dutch family with two additional alpha-gene defects: the common -alpha3.7 deletion and the rare IVS1-116 (A-->G) acceptor splice site mutation.

Giordano PC, Harteveld CL, Haak HL, Batelaan D, van Delft P, Plug RJ, Emonts M, Zanardini R, Bernini LF. Giordano PC, et al. Among authors: harteveld cl. Br J Haematol. 1998 Nov;103(2):370-6. doi: 10.1046/j.1365-2141.1998.00999.x. Br J Haematol. 1998. PMID: 9827907 Free article.

6

A complex haemoglobinopathy diagnosis in a family with both beta zero- and alpha (zero/+)-thalassaemia homozygosity.

Giordano PC, Harteveld CL, Bok LA, van Delft P, Batelaan D, Beemer FA, Bernini LF. Giordano PC, et al. Among authors: harteveld cl. Eur J Hum Genet. 1999 Feb-Mar;7(2):163-8. doi: 10.1038/sj.ejhg.5200281. Eur J Hum Genet. 1999. PMID: 10196699

7

Hb Aghia Sophia [alpha62(E11)Val-->0 (alpha1)], an "in-frame" deletion causing alpha-thalassemia.

Traeger-Synodinos J, Harteveld CL, Kanavakis E, Giordano PC, Kattamis C, Bernini LF. Traeger-Synodinos J, et al. Among authors: harteveld cl. Hemoglobin. 1999 Nov;23(4):317-24. doi: 10.3109/03630269909090747. Hemoglobin. 1999. PMID: 10569720

8

The second case of dominant beta-thalassemia induced by the codon 127 (CAG-->TAG) described as a de novo mutation in a Dutch boy.

Van Weel M, Harteveld CL, Bernini LF, Brouwers TM, Giordano PC. Van Weel M, et al. Among authors: harteveld cl. Hemoglobin. 1999 Nov;23(4):389-93. doi: 10.3109/03630269909090757. Hemoglobin. 1999. PMID: 10569730 No abstract available.

9

Haemoglobinopathy analyses in the Netherlands: a report of an in vitro globin chain biosynthesis survey using a rapid, modified method.

Giordano PC, Van Delft P, Batelaan D, Harteveld CL, Bernini LF. Giordano PC, et al. Among authors: harteveld cl. Clin Lab Haematol. 1999 Aug;21(4):247-56. doi: 10.1046/j.1365-2257.1999.00197.x. Clin Lab Haematol. 1999. PMID: 10583326

10

alpha-thalassaemia as a result of a novel splice donor site mutation of the alpha1-globin gene.

Harteveld CL, Beijer C, van Delft P, Zanardini R, Bernini LF, Giordano PC. Harteveld CL, et al. Br J Haematol. 2000 Sep;110(3):694-8. doi: 10.1046/j.1365-2141.2000.02225.x. Br J Haematol. 2000. PMID: 10997982 Free article.

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