Luo HY - Search Results

1

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

2

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. Am J Hematol. 2006 May;81(5):361-5. doi: 10.1002/ajh.20562. Am J Hematol. 2006. PMID: 16628724 Free article.

3

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. J Pediatr Hematol Oncol. 2004 Nov;26(11):773-6. doi: 10.1097/00043426-200411000-00019. J Pediatr Hematol Oncol. 2004. PMID: 15543018

4

Hemoglobin Titusville, a low oxygen affinity variant hemoglobin, in a family of Northern European background.

Luo HY, Irving I, Prior J, Lim E, Eung SH, Skelton TP, Erber WN, Steinberg MH, Chui DH. Luo HY, et al. Am J Hematol. 2004 Dec;77(4):384-6. doi: 10.1002/ajh.20209. Am J Hematol. 2004. PMID: 15551405 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: luo hy. Pediatr Blood Cancer. 2008 Feb;50(2):363-6. doi: 10.1002/pbc.20916. Pediatr Blood Cancer. 2008. PMID: 16732578

6

Sickle cell disease due to compound heterozygosity for Hb S and a novel 7.7-kb beta-globin gene deletion.

Andersson BA, Wering ME, Luo HY, Basran RK, Steinberg MH, Smith HP, Chui DH. Andersson BA, et al. Among authors: luo hy. Eur J Haematol. 2007 Jan;78(1):82-5. doi: 10.1111/j.1600-0609.2006.00771.x. Epub 2006 Oct 13. Eur J Haematol. 2007. PMID: 17038017

7

Hemoglobin SE disease: a concise review.

Masiello D, Heeney MM, Adewoye AH, Eung SH, Luo HY, Steinberg MH, Chui DH. Masiello D, et al. Among authors: luo hy. Am J Hematol. 2007 Jul;82(7):643-9. doi: 10.1002/ajh.20847. Am J Hematol. 2007. PMID: 17278112 Free article. Review.

8

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: luo hy. Pediatr Blood Cancer. 2007 Aug;49(2):207-10. doi: 10.1002/pbc.21269. Pediatr Blood Cancer. 2007. PMID: 17551985

9

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: luo hy. Am J Hematol. 2009 Jan;84(1):55-8. doi: 10.1002/ajh.21308. Am J Hematol. 2009. PMID: 19006227 Free article. Review.

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: luo hy. 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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