Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Kelvin C. K. Cheng"'
Autor:
Nelson C. N. Chan, Terry H. Y. Wong, Kelvin C. K. Cheng, Natalie P. H. Chan, Margaret H. L. Ng
Publikováno v:
Hemoglobin. 45:387-391
Publikováno v:
Hemoglobin. 45(6)
Prenatal screening of β-thalassemia (β-thal) carriers is based on the hallmark phenotype of microcytosis and raised Hb A
Autor:
June S Lau, Bonnie Kho, Joycelyn Sim, Arthur Kwok Leung Cheung, Margaret H.L. Ng, Jason C. C. So, Nicole Y Saw, Chi K Lau, Shek Y Lin, Anskar Y.H. Leung, Wing F Tang, Ho W Ip, Sze P Tsui, Tsan H Luk, Lai P Siu, Yok L. Kwong, Sze F Yip, Nelson K. L. Ng, Chi H Lin, Chunxiao Zhang, Cheuk H Man, Chun H Au, Harold K. K. Lee, Kelvin C K Cheng, Edmond S. K. Ma, Kit Fai Wong, Grace H W Cheng, Tsun Leung Chan, Stephen S. Y. Lam, Asif Javed, Suet Yi Leung
Publikováno v:
Blood Cancer Journal, Vol 10, Iss 10, Pp 1-5 (2020)
Blood Cancer Journal
Blood Cancer Journal
Autor:
Anskar Y.H. Leung, Ning Yang, Ho W Ip, Bonnie Kho, Jason C. C. So, Kelvin C K Cheng, Edmond S. K. Ma, Nelson K. L. Ng, Tsun Leung Chan, Shek Y Lin, Sze F Yip, Sze P Tsui, Margaret H.L. Ng, Stephen S. Y. Lam, Chunxiao Zhang, Harold K. K. Lee, June S. M. Lau, Kit Fai Wong, Tsan H Luk, Lisa L. P. Siu, Garret M. K. Leung, Yok L. Kwong, Chi K Lau, Chun H Au
Publikováno v:
American journal of hematology. 94(6)
The present study aimed to define a subtype of complex/monosomal karyotype (CK/MK) acute myeloid leukemia (AML) by its distinct clinical features, p53 signaling and responses to p53 targeting agents. Ninety-eight young adults (range: 21-60 years; med
Autor:
Michelle F W Chiu, Rico F Y Leung, Nelson C N Chan, Natalie P. H. Chan, Sequence S. H. Tang, Kin-Mang Lau, Margaret H.L. Ng, Rosalind Lie, Kelvin C K Cheng, King-Ho Chow
Publikováno v:
Hemoglobin. 41(4-6)
We report a novel HBB: c.114G>C mutation in a Chinese family. This mutation resulted in a β37(C3)Trp→Cys amino acid substitution and was synonymous with Hb Kent, a hemoglobin (Hb) variant that was reported exclusively in patients of European desce
Publikováno v:
Hemoglobin. 40(6)
Genetic association studies showed that Hb F is under the influence of major quantitative trait loci (QTL) in β-thalassemia (β-thal) carriers. Single nucleotide polymorphisms (SNPs) at three major QTLs, BCL11A, HBS1L-MYB intergenic region and XmnI-
Autor:
Tommy W.F. Tang, Anskar Y.H. Leung, Chi Kuen Lau, Sze Fai Yip, Bonnie Kho, Kelvin C K Cheng, Edmond S. K. Ma, Tsan-Hei Luk, Jason C. C. So, Chun Hang Au, Kit Fai Wong, Christopher Chan, Sy Lin, Yok-Lam Kwong, Lisa L. P. Siu, Harold K. K. Lee, Szeman June Lau, Chunxiao Zhang, Ho-Wan Ip, Margaret H.L. Ng, Sze Pui Tsui
Publikováno v:
Blood. 132:5267-5267
Background. Acute myeloid leukaemia (AML) is a group of heterogeneous diseases with distinct clinicopathologic, cytogenetic and genetic features, sharing in common an abnormal increase in myeloblasts in blood or bone marrow (BM). Induction and consol
Autor:
Nelson C N Chan, Johnny K F Ma, Vivien Mak, Stephen C C Choy, Kelvin C K Cheng, Joyce H. Y. Kwong, Natalie P. H. Chan, Margaret H.L. Ng, Kate F.S. Leung, Michael L. G. Wong, Carmen K M Ng, Harold K. K. Lee, Daniel H F Fong, Ka Lok Luke Chan
Publikováno v:
Blood. 132:4900-4900
Introduction: Non-transfusion dependent thalassemia (NTDT) includes HbH disease, β-thalassemia intermedia (β-TI) and HbE/β-thalassemia. The transfusion requirements of patients with NTDT are variable and they are all at risk of developing iron ove
Autor:
Kelvin C K Cheng, Wai-Shan Wong, Chi Kong Li, Ki Wai Chik, Matthew M. K. Shing, Suk Hang Cheng, Margaret H.L. Ng, Kin-Mang Lau, Natalie P. H. Chan
Publikováno v:
Leukemia Research. 31:235-238
We describe a case of coexisting BCR-ABL negative myeloproliferative disorder and precursor T-cell lymphoblastic lymphoma associated with t(8;13) involving FGFR1 at 8p11 in a 14-year-old boy who presented with generalized lymphadenopathy and an abdom