Chui DH - Search Results

1

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. Among authors: chui dh. Pediatr Blood Cancer. 2007 Aug;49(2):207-10. doi: 10.1002/pbc.21269. Pediatr Blood Cancer. 2007. PMID: 17551985

2

Novel dominant β-thalassemia: Hb Boston-Kuwait [codon 139/140(+T)].

Croteau SE, Luo HY, Lehmann LE, Chui DH, Neufeld EJ. Croteau SE, et al. Among authors: chui dh. Pediatr Blood Cancer. 2013 Oct;60(10):E131-4. doi: 10.1002/pbc.24611. Epub 2013 Jun 15. Pediatr Blood Cancer. 2013. PMID: 23776097

3

Hereditary Persistence of Fetal Hemoglobin Caused by Single Nucleotide Promoter Mutations in Sickle Cell Trait and Hb SC Disease.

Akinbami AO, Campbell AD, Han ZJ, Luo HY, Chui DH, Steinberg MH. Akinbami AO, et al. Among authors: chui dh. Hemoglobin. 2016;40(1):64-5. doi: 10.3109/03630269.2015.1080725. Epub 2015 Sep 15. Hemoglobin. 2016. PMID: 26372199

4

Hemoglobinopathies mimicking Hb S/beta-thalassemia: Hb S/S with alpha-thalassemia and Hb S/Volga.

Luo HY, Heeney M, Wang WC, Eung SH, Ware RE, Steinberg MH, Chui DH. Luo HY, et al. Among authors: chui dh. Am J Hematol. 2006 May;81(5):361-5. doi: 10.1002/ajh.20562. Am J Hematol. 2006. PMID: 16628724 Free article.

5

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. Among authors: chui dh. Pediatr Blood Cancer. 2008 Feb;50(2):363-6. doi: 10.1002/pbc.20916. Pediatr Blood Cancer. 2008. PMID: 16732578

6

A novel sickle hemoglobin: hemoglobin S-south end.

Luo HY, Adewoye AH, Eung SH, Skelton TP, Quillen K, McMahon L, Steinberg MH, Chui DH. Luo HY, et al. Among authors: chui dh. J Pediatr Hematol Oncol. 2004 Nov;26(11):773-6. doi: 10.1097/00043426-200411000-00019. J Pediatr Hematol Oncol. 2004. PMID: 15543018

7

Hemoglobin Kenya composed of alpha- and ((A)gammabeta)-fusion-globin chains, associated with hereditary persistence of fetal hemoglobin.

Wilcox I, Boettger K, Greene L, Malek A, Davis L, Steinberg MH, Luo HY, Chui DH. Wilcox I, et al. Among authors: chui dh. Am J Hematol. 2009 Jan;84(1):55-8. doi: 10.1002/ajh.21308. Am J Hematol. 2009. PMID: 19006227 Free article. Review.

8

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. Among authors: chui dh. Am J Hematol. 2009 Sep;84(9):603-6. doi: 10.1002/ajh.21480. Am J Hematol. 2009. PMID: 19650141 Free article.

9

A 3-bp deletion in the HBS1L-MYB intergenic region on chromosome 6q23 is associated with HbF expression.

Farrell JJ, Sherva RM, Chen ZY, Luo HY, Chu BF, Ha SY, Li CK, Lee AC, Li RC, Li CK, Yuen HL, So JC, Ma ES, Chan LC, Chan V, Sebastiani P, Farrer LA, Baldwin CT, Steinberg MH, Chui DH. Farrell JJ, et al. Among authors: chui dh. Blood. 2011 May 5;117(18):4935-45. doi: 10.1182/blood-2010-11-317081. Epub 2011 Mar 8. Blood. 2011. PMID: 21385855 Free PMC article.

10

Severe fetal and neonatal hemolytic anemia due to a 198 kb deletion removing the complete β-globin gene cluster.

Verhovsek M, Shah NR, Wilcox I, Koenig SC, Barros T, Thornburg CD, Steinberg MH, Luo HY, Chui DH. Verhovsek M, et al. Among authors: chui dh. Pediatr Blood Cancer. 2012 Nov;59(5):941-4. doi: 10.1002/pbc.24094. Epub 2012 Jan 31. Pediatr Blood Cancer. 2012. PMID: 22294483

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