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Pediatric Transplantation|April 9, 2022
Successful haploidentical hematopoietic stem cell transplantation (HSCT) and durable engraftment by repeated donor lymphocyte infusions for a Chinese patient with transfusion-dependent hemoglobin (Hb) Hammersmith and massive splenomegalyWilson Y K Chan, Nelson C N Chan, Jason C C So, et al.
Frontiers in Oncology|April 10, 2024
Case report: Therapy-related myeloid neoplasms in three pediatric cases with medulloblastomaLi Shun Mak, Xiuling Li, Wilson Y K Chan, et al.
American Journal of Hematology|August 4, 2009
Sickle cell disease caused by heterozygosity for Hb S and novel LCR deletion: Report of two patientsSara C Koenig, Esmira Becirevic, Miriam S C Hellberg, et al.
Journal of Medical Microbiology|March 5, 2011
Pneumococcal native aortic valve endocarditis with mycotic abdominal aortic aneurysm, paraspinal and iliopsoas abscesses and pneumonia revealing a multiple myelomaJasper F W Chan, Gloria Y Y Hwang, Sophia Lamb, et al.
Blood Cells, Molecules & Diseases|August 12, 2008
BCL11A is a major HbF quantitative trait locus in three different populations with beta-hemoglobinopathiesAmanda E Sedgewick, Nadia Timofeev, Paola Sebastiani, et al.
Annals of Hematology|December 6, 2018
Next-generation sequencing with a 54-gene panel identified unique mutational profile and prognostic markers in Chinese patients with myelofibrosisHarinder Gill, Ho-Wan Ip, Rita Yim, et al.
American Journal of Hematology|February 13, 2008
Variation and heritability of Hb F and F-cells among beta-thalassemia heterozygotes in Hong KongGeoffrey T Gibney, Carolien I M Panhuysen, Jason C C So, et al.
Blood|March 10, 2011
A 3-bp deletion in the HBS1L-MYB intergenic region on chromosome 6q23 is associated with HbF expressionJohn J Farrell, Richard M Sherva, Zhi-Yi Chen, et al.
Science Advances|November 25, 2015
Pim kinases modulate resistance to FLT3 tyrosine kinase inhibitors in FLT3-ITD acute myeloid leukemiaAlexa S Green, Thiago T Maciel, Marie-Anne Hospital, et al.
American Journal of Hematology|March 23, 2019
Distinct mutation spectrum, clinical outcome and therapeutic responses of typical complex/monosomy karyotype acute myeloid leukemia carrying TP53 mutationsGarret M K Leung, Chunxiao Zhang, Nelson K L Ng, et al.
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