Harteveld CL - Search Results

1

The first report of hemoglobin E in combination with the highly unstable alpha-globin variant Hb Adana: The importance of molecular confirmation.

Achour A, de Grouw E, van Erp F, Arkesteijn S, Schaap R, Huurne JT, Bisoen S, Verschuren M, Harteveld CL. Achour A, et al. Among authors: harteveld cl. Int J Lab Hematol. 2019 Jun;41(3):e76-e78. doi: 10.1111/ijlh.12965. Epub 2019 Jan 20. Int J Lab Hematol. 2019. PMID: 30663218 Free PMC article. No abstract available.

2

Hb Kurdistan [alpha 47(CE5)Asp-->Tyr], a new alpha chain variant in combination with beta (0)-thalassemia.

Giordano PC, Harteveld CL, Streng H, Oosterwijk JC, Heister JG, Amons R, Bernini LF. Giordano PC, et al. Among authors: harteveld cl. Hemoglobin. 1994 Jan;18(1):11-8. doi: 10.3109/03630269409014141. Hemoglobin. 1994. PMID: 8195005

3

Hb Utrecht [alpha 2 129(H12)Leu-->Pro], a new unstable alpha 2-chain variant associated with a mild alpha-thalassaemic phenotype.

Harteveld CL, Giordano PC, Losekoot M, Heister JG, Batelaan D, van Delft P, Bruin MC, Bernini LF. Harteveld CL, et al. Br J Haematol. 1996 Sep;94(3):483-5. doi: 10.1046/j.1365-2141.1996.d01-1828.x. Br J Haematol. 1996. PMID: 8790146

4

Hb Malmö [beta-97(FG-4)His-->Gln] leading to polycythemia in a Dutch family.

Giordano PC, Harteveld CL, Brand A, Willems LN, Kluin-Nelemans HC, Plug RJ, Batelaan DN, Bernini LF. Giordano PC, et al. Among authors: harteveld cl. Ann Hematol. 1996 Oct;73(4):183-8. doi: 10.1007/s002770050225. Ann Hematol. 1996. PMID: 8890707

5

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

6

Hb Groene Hart: a new Pro-->Ser amino acid substitution at position 119 of the alpha1-globin chain is associated with a mild alpha-thalassemia phenotype.

Harteveld CL, van Delft P, Plug R, Versteegh FG, Hagen B, van Rooijen I, Kok PJ, Wajcman H, Kister J, Giordano PC. Harteveld CL, et al. Hemoglobin. 2002 Aug;26(3):255-60. doi: 10.1081/hem-120015029. Hemoglobin. 2002. PMID: 12403490

7

Molecular spectrum of alpha-thalassemia in the Iranian population of Hormozgan: three novel point mutation defects.

Harteveld CL, Yavarian M, Zorai A, Quakkelaar ED, van Delft P, Giordano PC. Harteveld CL, et al. Am J Hematol. 2003 Oct;74(2):99-103. doi: 10.1002/ajh.10385. Am J Hematol. 2003. PMID: 14508795 Free article.

8

Hb Buffalo [alpha89(FG1)His-->Gln (alpha1)], observed solely and in the presence of an Hb S [beta6(A3)Glu-->Val] heterozygosity.

Harteveld CL, Van Delft P, Akkermans N, Arkesteijn S, Van Rooijen-Nijdam IH, Kok PJ, Versteegh FG, Giordano PC. Harteveld CL, et al. Hemoglobin. 2004 Aug;28(3):223-7. doi: 10.1081/hem-200029150. Hemoglobin. 2004. PMID: 15481890

9

Hb zoeterwoude [beta23(B5)Val-->Ala)]: a new beta-globin variant found in association with erythrocytosis.

Harteveld CL, Groeneveld JH, van Dam B, Van Delft P, Akkerman N, Arkesteijn S, Giordano PC. Harteveld CL, et al. Hemoglobin. 2005;29(1):11-7. Hemoglobin. 2005. PMID: 15768551

10

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: harteveld cl. Hemoglobin. 2005;29(1):43-50. Hemoglobin. 2005. PMID: 15768554

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