Luo HY - Search Results

1

Hb A2 Hong Kong - A novel δ-globin variant in a Chinese family masks the diagnosis of β-thalassemia trait.

So CC, Chan AY, Luo HY, Verhovsek M, Chui DH, Ling SC, Chan LC. So CC, et al. Among authors: luo hy. Hemoglobin. 2011;35(2):162-5. doi: 10.3109/03630269.2011.557172. Hemoglobin. 2011. PMID: 21417575

2

Hb Hope [beta136(H14)Gly-->Asp (GGT-->GAT)]: interactions with Hb S [beta6(A3)Glu-->Val (GAG-->GTG)], other variant hemoglobins and thalassemia.

Ingle J, Adewoye A, Dewan R, Okoli M, Rollins L, Eung SH, Luo HY, Chui DH, Steinberg MH. Ingle J, et al. Among authors: luo hy. Hemoglobin. 2004;28(4):277-85. doi: 10.1081/hem-200037801. Hemoglobin. 2004. PMID: 15658184 Review.

3

New and known β-thalassemia determinants masked by known and new δ gene defects [Hb A(2)-Ramallah or δ6(A3)Glu→Gln, GAG>>CAG].

Phylipsen M, Harteveld CL, de Metz M, Gallivan MV, Arkesteijn SG, Luo HY, Chui DH, Giordano PC. Phylipsen M, et al. Among authors: luo hy. Hemoglobin. 2010;34(5):445-50. doi: 10.3109/03630269.2010.511591. Hemoglobin. 2010. PMID: 20854118

4

Identification of the first mutation in a BRE motif of the β-globin gene and its inheritance with two other α-globin gene mutations in a Lebanese family.

Inati A, Abbas HA, Al-Danaf J, Souaid M, Kahale M, Koussa S, Abou Nasr T, Davis L, Luo HY, Chui DH. Inati A, et al. Among authors: luo hy. Hemoglobin. 2013;37(2):171-5. doi: 10.3109/03630269.2013.772523. Hemoglobin. 2013. PMID: 23470150

5

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: luo hy. Pediatr Blood Cancer. 2013 Oct;60(10):E131-4. doi: 10.1002/pbc.24611. Epub 2013 Jun 15. Pediatr Blood Cancer. 2013. PMID: 23776097

6

Hb Youngstown [β101(G3)Glu → Ala; HBB: c.305A > C]: An unstable hemoglobin variant causing severe hemolytic anemia.

Edward HL, Pisani LA, Rodriguez-Romero WE, Chaves-Villalobos J, Garcia-Quesada J, Harris NS, Luo HY, Steinberg MH, Forget BG, Chui DH. Edward HL, et al. Among authors: luo hy. Hemoglobin. 2014;38(6):381-4. doi: 10.3109/03630269.2014.971960. Epub 2014 Oct 27. Hemoglobin. 2014. PMID: 25347256

7

The first report of a homozygous codons 9/10 (+T) β-thalassemia mutation in a Turkish patient.

Unal S, Chui DH, Luo HY, Okur H, Oymak Y, Gumruk F. Unal S, et al. Among authors: luo hy. Hemoglobin. 2015;39(1):66-8. doi: 10.3109/03630269.2014.982255. Epub 2015 Jan 9. Hemoglobin. 2015. PMID: 25572182

8

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: luo hy. Hemoglobin. 2016;40(1):64-5. doi: 10.3109/03630269.2015.1080725. Epub 2015 Sep 15. Hemoglobin. 2016. PMID: 26372199

9

Diverse hematological phenotypes of β-thalassemia carriers.

Luo HY, Chui DH. Luo HY, et al. Ann N Y Acad Sci. 2016 Mar;1368(1):49-55. doi: 10.1111/nyas.13056. Epub 2016 Apr 28. Ann N Y Acad Sci. 2016. PMID: 27123947 Review.

10

Hb Presbyterian (HBB: c.327C>G) in a Nicaraguan Family.

Pernudy-Ubau A, Salinas-Molina J, Requenez Y, Ortiz-Lopez M, Puller AC, García-Rosales K, Rodríguez-Estrada A, Rodríguez-Romero W, Mejía-Baltodano G, Luo HY, Chui DHK. Pernudy-Ubau A, et al. Among authors: luo hy. Hemoglobin. 2017 Jan;41(1):50-52. doi: 10.1080/03630269.2017.1302949. Epub 2017 Apr 11. Hemoglobin. 2017. PMID: 28395541

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