Detalhe da pesquisa
1.
Analysis of clinical and genomic profiles of therapy-related myeloid neoplasm in Korea.
Hum Genomics
; 17(1): 13, 2023 02 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-36814285
2.
Telomere integrated scoring system of myelodysplastic syndrome.
J Clin Lab Anal
; 37(3): e24839, 2023 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-36658792
3.
Application of Interphase Fluorescent in Situ Hybridization: a Screening Tool for the Diagnosis of Microdeletion Syndrome.
Clin Lab
; 68(4)2022 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35443603
4.
Successful Treatment of Pediatric Epstein-Barr Virus-positive Aggressive Natural Killer-Cell Leukemia.
J Pediatr Hematol Oncol
; 41(5): e336-e337, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29889803
5.
The risk of second primary malignancy is increased in differentiated thyroid cancer patients with a cumulative (131)I dose over 37 GBq.
Clin Endocrinol (Oxf)
; 83(1): 117-23, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25115234
6.
Fluorescence in situ hybridization panel for monitoring of minimal residual disease in patients with double minute chromosomes.
Blood Cells Mol Dis
; 52(4): 208-13, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24211232
7.
Chromosome 13 deletion and hypodiploidy on conventional cytogenetics are robust prognostic factors in Korean multiple myeloma patients: web-based multicenter registry study.
Ann Hematol
; 93(8): 1353-61, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24671365
8.
Multiple Primary Cancers With Hematologic Malignancies and Germline Predisposition: A Case Series.
Ann Lab Med
; 44(5): 446-449, 2024 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38449380
9.
Quantitative comparison of CDKN2B methylation in pediatric and adult myelodysplastic syndromes.
Acta Haematol
; 130(2): 115-21, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23571652
10.
Cryptic KMT2A/MLLT10 fusion detected by next-generation sequencing in a case of pediatric acute megakaryoblastic leukemia.
Cancer Genet
; 276-277: 36-39, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37478796
11.
Hema-seq reveals genomic aberrations in a rare simultaneous occurrence of hematological malignancies.
Cell Rep Methods
; 3(10): 100617, 2023 Oct 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-37852254
12.
Polymorphisms in genes that regulate cyclosporine metabolism affect cyclosporine blood levels and clinical outcomes in patients who receive allogeneic hematopoietic stem cell transplantation.
Biol Blood Marrow Transplant
; 18(1): 37-43, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-21896346
13.
Sequential vincristine, adriamycin, dexamethasone (VAD) followed by bortezomib, thalidomide, dexamethasone (VTD) as induction, followed by high-dose therapy with autologous stem cell transplant and consolidation therapy with bortezomib for newly diagnosed multiple myeloma: results of a phase II trial.
Ann Hematol
; 91(2): 249-56, 2012 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-21789621
14.
Impact of vitamin D receptor gene polymorphisms on clinical outcomes of HLA-matched sibling hematopoietic stem cell transplantation.
Clin Transplant
; 26(3): 476-83, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22035017
15.
Clinical and Genomic Profiles of Korean Patients with MECOM Rearrangement and the t(3;21)(q26.2;q22.1) Translocation.
Ann Lab Med
; 42(5): 590-596, 2022 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35470277
16.
Genetic profile of primary plasma cell leukemia in Korea: comparison with plasma cell myeloma.
Leuk Lymphoma
; 63(2): 385-394, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34592901
17.
Increased Apoptotic Activity in Low-Risk Myelodysplastic Syndrome.
J Clin Med
; 11(15)2022 Aug 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35956220
18.
The importance of critically short telomere in myelodysplastic syndrome.
Biomark Res
; 10(1): 79, 2022 Nov 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-36357941
19.
Novel THPO variant in hereditary thrombocytopenia: A potential candidate variant for predisposition to myeloid neoplasm.
PLoS One
; 17(12): e0271624, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36534659
20.
Heterogeneous genetic landscape of congenital neutropenia in Korean patients revealed by whole exome sequencing: genetic, phenotypic and histologic correlations.
Sci Rep
; 12(1): 7515, 2022 05 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35525891