Chui DHK - Search Results

1

The clinical severity of hemoglobin S/Black (^A γδβ)⁰ -thalassemia.

Cancio MI, Aygun B, Chui DHK, Rothman JA, Scott JP, Estepp JH, Hankins JS. Cancio MI, et al. Among authors: chui dhk. Pediatr Blood Cancer. 2017 Nov;64(11):10.1002/pbc.26596. doi: 10.1002/pbc.26596. Epub 2017 Apr 28. Pediatr Blood Cancer. 2017. PMID: 28453928 Free PMC article.

2

Fetal haemoglobin levels and haematological characteristics of compound heterozygotes for haemoglobin S and deletional hereditary persistence of fetal haemoglobin.

Ngo DA, Aygun B, Akinsheye I, Hankins JS, Bhan I, Luo HY, Steinberg MH, Chui DH. Ngo DA, et al. Br J Haematol. 2012 Jan;156(2):259-64. doi: 10.1111/j.1365-2141.2011.08916.x. Epub 2011 Oct 24. Br J Haematol. 2012. PMID: 22017641 Free PMC article.

3

Clinical phenotypes of three children with sickle cell disease caused by HbS/Sicilian (δβ)⁰ -thalassemia deletion.

Aygun B, Bello A, Thompson AA, Davis L, Sun Y, Luo HY, Cui S, Chui DHK. Aygun B, et al. Among authors: chui dhk. Am J Hematol. 2022 Apr;97(4):E156-E158. doi: 10.1002/ajh.26470. Epub 2022 Jan 26. Am J Hematol. 2022. PMID: 35045200 Free article. No abstract available.

4

Fetal hemoglobin in sickle cell anemia.

Akinsheye I, Alsultan A, Solovieff N, Ngo D, Baldwin CT, Sebastiani P, Chui DH, Steinberg MH. Akinsheye I, et al. Blood. 2011 Jul 7;118(1):19-27. doi: 10.1182/blood-2011-03-325258. Epub 2011 Apr 13. Blood. 2011. PMID: 21490337 Free PMC article. Review.

5

Sickle cell disease caused by heterozygosity for Hb S and novel LCR deletion: Report of two patients.

Koenig SC, Becirevic E, Hellberg MS, Li MY, So JC, Hankins JS, Ware RE, McMahon L, Steinberg MH, Luo HY, Chui DH. Koenig SC, et al. Am J Hematol. 2009 Sep;84(9):603-6. doi: 10.1002/ajh.21480. Am J Hematol. 2009. PMID: 19650141 Free article.

6

Sickle cell disease caused by Hb S/Québec-CHORI: treatment with hydroxyurea and response.

Tubman VN, Bennett CM, Luo HY, Chui DH, Heeney MM. Tubman VN, et al. Pediatr Blood Cancer. 2007 Aug;49(2):207-10. doi: 10.1002/pbc.21269. Pediatr Blood Cancer. 2007. PMID: 17551985

7

A Mild Phenotype of Severe β+ Thalassemia in a 16-Month-Old Boy.

Akinbami AO, Sobota AE, Luo HY, Chui DHK, Steinberg MH. Akinbami AO, et al. Among authors: chui dhk. J Pediatr Hematol Oncol. 2018 Apr;40(3):e145-e147. doi: 10.1097/MPH.0000000000001068. J Pediatr Hematol Oncol. 2018. PMID: 29309373

8

Beta-thalassemia intermedia due to compound heterozygosity for two beta-globin gene promoter mutations, including a novel TATA box deletion.

Basran RK, Reiss UM, Luo HY, Ware RE, Chui DH. Basran RK, et al. Pediatr Blood Cancer. 2008 Feb;50(2):363-6. doi: 10.1002/pbc.20916. Pediatr Blood Cancer. 2008. PMID: 16732578

9

Massive splenic infarction in an adolescent with hemoglobin S-HPFH.

Whyte D, Forget B, Chui DH, Luo HY, Pashankar F. Whyte D, et al. Pediatr Blood Cancer. 2013 Jul;60(7):E49-51. doi: 10.1002/pbc.24444. Epub 2012 Dec 31. Pediatr Blood Cancer. 2013. PMID: 23281181

10

Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5' olfactory receptor gene cluster.

Solovieff N, Milton JN, Hartley SW, Sherva R, Sebastiani P, Dworkis DA, Klings ES, Farrer LA, Garrett ME, Ashley-Koch A, Telen MJ, Fucharoen S, Ha SY, Li CK, Chui DH, Baldwin CT, Steinberg MH. Solovieff N, et al. Blood. 2010 Mar 4;115(9):1815-22. doi: 10.1182/blood-2009-08-239517. Epub 2009 Dec 16. Blood. 2010. PMID: 20018918 Free PMC article.

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