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Identification of a novel mutation in the GLUT2 gene in a patient with Fanconi-Bickel syndrome presenting with neonatal diabetes mellitus and galactosaemia.
- Published in:
- 2002
- By:
- Publication type:
- journal article
Rare Case of Accelerated-Phase Chronic Myeloid Leukemia Diagnosed During Treatment for JAK2 V617F–Positive Primary Myelofibrosis.
- Published in:
- Laboratory Medicine, 2022, v. 53, n. 6, p. e140, doi. 10.1093/labmed/lmac011
- By:
- Publication type:
- Article
Emergence of a BCR::ABL1 rearrangement following a uniquely complex clonal evolution pattern in a patient undergoing Fms‐like tyrosine kinase 3 inhibitor therapy for acute myeloid leukemia.
- Published in:
- 2023
- By:
- Publication type:
- Letter to the Editor
Comparison of clinical and laboratory characteristics of nonsecretory multiple myeloma and secretory multiple myeloma in a tertiary care hospital.
- Published in:
- International Journal of Laboratory Hematology, 2022, v. 44, n. 3, p. 582, doi. 10.1111/ijlh.13811
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- Publication type:
- Article
Recent advances in cytogenetic characterization of multiple myeloma.
- Published in:
- International Journal of Laboratory Hematology, 2019, v. 41, n. 1, p. 5, doi. 10.1111/ijlh.12882
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- Publication type:
- Article
Comparison of clinicopathologic findings according to JAK2 V617F mutation in patients with essential thrombocythemia.
- Published in:
- 2009
- By:
- Publication type:
- journal article
A Patient With CD20-positive T-cell Lymphoma Concurrently Exhibiting B-cell Neoplasm-related Genetic Abnormalities Shows Clonal Escape Post CD20-targeting Treatment.
- Published in:
- Annals of Laboratory Medicine, 2023, v. 43, n. 2, p. 200, doi. 10.3343/alm.2023.43.2.200
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- Publication type:
- Article
Bone Marrow Findings in Patients With Ewing Sarcoma/Primitive Neuroectodermal Tumor.
- Published in:
- Annals of Laboratory Medicine, 2021, v. 41, n. 5, p. 499, doi. 10.3343/alm.2021.41.5.499
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- Publication type:
- Article
Immune Checkpoint Programmed Cell Death Protein-1 (PD-1) Expression on Bone Marrow T Cell Subsets in Patients With Plasma Cell Myeloma.
- Published in:
- Annals of Laboratory Medicine, 2021, v. 41, n. 3, p. 259, doi. 10.3343/alm.2021.41.3.259
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- Publication type:
- Article
Clinical, Laboratory, and Bone Marrow Findings of 31 Patients With Waldenström Macroglobulinemia.
- Published in:
- Annals of Laboratory Medicine, 2020, v. 40, n. 3, p. 193, doi. 10.3343/alm.2020.40.3.193
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- Publication type:
- Article
First Case of Double T-Cell Receptor Alpha/Delta Rearrangements of t(11;14) and inv(14) and Subsequent JAK2 Rearrangement in a Patient With T-cell Acute Lymphoblastic Leukemia.
- Published in:
- Annals of Laboratory Medicine, 2020, v. 40, n. 1, p. 76, doi. 10.3343/alm.2020.40.1.76
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- Publication type:
- Article
JL1 Antigen Expression on Bone Marrow Lymphoma Cells from Patients With Non-Hodgkin Lymphoma.
- Published in:
- Annals of Laboratory Medicine, 2020, v. 40, n. 1, p. 1, doi. 10.3343/alm.2020.40.1.1
- By:
- Publication type:
- Article
POEMS Syndrome: Bone Marrow, Laboratory, and Clinical Findings in 24 Korean Patients.
- Published in:
- Annals of Laboratory Medicine, 2019, v. 39, n. 6, p. 561, doi. 10.3343/alm.2019.39.6.561
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- Publication type:
- Article
Two Rare Cases of Therapy-Related Acute Lymphoblastic Leukemia in Patients With Plasma Cell Myeloma.
- Published in:
- 2019
- By:
- Publication type:
- Letter to the Editor
Clinical and Cytogenetic Profiles of Rhabdomyosarcoma with Bone Marrow Involvement in Korean Children: A 15-Year Single-Institution Experience.
- Published in:
- Annals of Laboratory Medicine, 2018, v. 38, n. 2, p. 132, doi. 10.3343/alm.2018.38.2.132
- By:
- Publication type:
- Article
A Case of Primary Bone Marrow Diffuse Large B-cell Lymphoma Presenting With Fibrillar Projections and Hemophagocytic Lymphohistiocytosis.
- Published in:
- 2017
- By:
- Publication type:
- Case Study
A Case of Acute Myeloid Leukemia Concurrent With Untreated Chronic Lymphocytic Leukemia.
- Published in:
- Annals of Laboratory Medicine, 2017, v. 37, n. 4, p. 336, doi. 10.3343/alm.2017.37.4.336
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- Publication type:
- Article
The First Case of Therapy-Related Myelomastocytic Leukemia Based on the WHO 2008 Classification and the Recently Proposed Diagnostic Criteria.
- Published in:
- 2017
- By:
- Publication type:
- Case Study
Familial Hemophagocytic Lymphohistiocytosis Type 2 in a Korean Infant With Compound Heterozygous PRF1 Defects Involving a PRF1 Mutation, c.1091T>G.
- Published in:
- 2017
- By:
- Publication type:
- Case Study
Patient-derived multicellular tumor spheroids towards optimized treatment for patients with hepatocellular carcinoma.
- Published in:
- Journal of Experimental & Clinical Cancer Research (17569966), 2018, v. 37, n. 1, p. N.PAG, doi. 10.1186/s13046-018-0752-0
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- Publication type:
- Article
Identification of the mechanism underlying a human chimera by SNP array analysis.
- Published in:
- American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 9, p. 2119, doi. 10.1002/ajmg.a.35476
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- Publication type:
- Article
Clinical implications and genetic features of clonal cytopenia of undetermined significance compared to lower‐risk myelodysplastic syndrome.
- Published in:
- British Journal of Haematology, 2022, v. 198, n. 4, p. 703, doi. 10.1111/bjh.18273
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- Publication type:
- Article
Clinical and Functional Characteristics of a Novel Heterozygous Mutation of the IGF1R Gene and IGF1R Haploinsufficiency due to Terminal 15q26.2->qter Deletion in Patients with Intrauterine Growth Retardation and Postnatal Catch-Up Growth Failure.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2011, v. 96, n. 1, p. E130, doi. 10.1210/jc.2010-1789
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- Publication type:
- Article
VLA-4 and CXCR4 expression levels show contrasting prognostic impact (favorable and unfavorable, respectively) in acute myeloid leukemia.
- Published in:
- Annals of Hematology, 2015, v. 94, n. 10, p. 1631, doi. 10.1007/s00277-015-2442-8
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- Publication type:
- Article
Monosomal karyotype in acute myeloid leukemia and the role of allogeneic hematopoietic cell transplantation.
- Published in:
- Annals of Hematology, 2015, v. 94, n. 5, p. 795, doi. 10.1007/s00277-014-2286-7
- By:
- Publication type:
- Article
An illustrative case of t(14;19)/BCL3 rearrangement as a karyotypic evolution of chronic lymphocytic leukemia.
- Published in:
- 2013
- By:
- Publication type:
- Journal Article
An illustrative case of t(14;19)/<i>BCL3</i> rearrangement as a karyotypic evolution of chronic lymphocytic leukemia.
- Published in:
- 2013
- By:
- Publication type:
- Letter
Double-hit myeloma with IGH/MYC and IGH/CCND1 translocations.
- Published in:
- 2013
- By:
- Publication type:
- Journal Article
Double-hit myeloma with IGH/ MYC and IGH/ CCND1 translocations.
- Published in:
- 2013
- By:
- Publication type:
- Letter
Differences in PD-1 expression on CD8+ T-cells in chronic myeloid leukemia patients according to disease phase and TKI medication.
- Published in:
- Cancer Immunology, Immunotherapy, 2020, v. 69, n. 11, p. 2223, doi. 10.1007/s00262-020-02617-5
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- Publication type:
- Article
Increased circulating plasma cells detected by flow cytometry predicts poor prognosis in patients with plasma cell myeloma.
- Published in:
- Cytometry. Part B, 2018, v. 94, n. 3, p. 493, doi. 10.1002/cyto.b.21606
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- Publication type:
- Article
Frequency and Clinicopathologic Features of RUNX1 Mutations in Patients With Acute Myeloid Leukemia Not Otherwise Specified.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Distinct features of angioimmunoblastic T-cell lymphoma with bone marrow involvement.
- Published in:
- American Journal of Clinical Pathology, 2009, v. 131, n. 5, p. 640, doi. 10.1309/AJCPQXKCHQH4VAJ5
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- Publication type:
- Article
Cytogenetic classification in Korean multiple myeloma patients: prognostic significance of hyperdiploidy with 47-50 chromosomes and the number of structural abnormalities.
- Published in:
- European Journal of Haematology, 2014, v. 92, n. 4, p. 313, doi. 10.1111/ejh.12257
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- Publication type:
- Article
The Rho-associated kinase inhibitor fasudil can replace Y-27632 for use in human pluripotent stem cell research.
- Published in:
- PLoS ONE, 2020, v. 15, n. 5, p. 1, doi. 10.1371/journal.pone.0233057
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- Publication type:
- Article
Pathological roles of the VEGF/SphK pathway in Niemann-Pick type C neurons.
- Published in:
- Nature Communications, 2014, v. 5, n. 11, p. 5514, doi. 10.1038/ncomms6514
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- Publication type:
- Article
Clinicopathologic characteristics and clinical outcome of multiple myeloma with del(17p): A retrospective analysis of single center experience for 12 years.
- Published in:
- Clinical Lymphoma, Myeloma & Leukemia, 2019, v. 19, p. e60, doi. 10.1016/j.clml.2019.09.093
- By:
- Publication type:
- Article
The CCR5 (−2135C/T) Polymorphism may be Associated with the Development of Kawasaki Disease in Korean Children.
- Published in:
- Journal of Clinical Immunology, 2009, v. 29, n. 1, p. 22, doi. 10.1007/s10875-008-9218-z
- By:
- Publication type:
- Article
Two cases of post-liver transplant acute myeloid leukemia in Korean adults: review of bibliographies and comparison with post-renal transplant acute myeloid leukemia.
- Published in:
- 2008
- By:
- Publication type:
- Letter
Clinical characteristics and disease progression of retinitis pigmentosa associated with PDE6B mutations in Korean patients.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41598-020-75902-z
- By:
- Publication type:
- Article
Is Whole Exome Sequencing Clinically Practical in the Management of Pediatric Crohn's Disease?
- Published in:
- Gut & Liver, 2015, v. 9, n. 6, p. 767, doi. 10.5009/gnl15176
- By:
- Publication type:
- Article
Genomic Profile of Chronic Lymphocytic Leukemia in Korea Identified by Targeted Sequencing.
- Published in:
- PLoS ONE, 2016, v. 11, n. 12, p. 1, doi. 10.1371/journal.pone.0167641
- By:
- Publication type:
- Article
Endocrine dysfunctions in children with Williams- Beuren syndrome.
- Published in:
- Annals of Pediatric Endocrinology & Metabolism, 2016, v. 21, n. 1, p. 15, doi. 10.6065/apem.2016.21.1.15
- By:
- Publication type:
- Article
Turner syndrome presented with tall stature due to overdosage of the SHOX gene.
- Published in:
- 2015
- By:
- Publication type:
- Case Study
Current Status of Clinical Diagnosis and Genetic Analysis of Hereditary Hemorrhagic Telangiectasia in South Korea: Multicenter Case Series and a Systematic Review.
- Published in:
- Neurointervention, 2019, v. 14, n. 2, p. 91, doi. 10.5469/neuroint.2019.00150
- By:
- Publication type:
- Article
Molecular cytogenetic and clinical characterization of a patient with a 5.6-Mb deletion in 7p15 including HOXA cluster.
- Published in:
- American Journal of Medical Genetics. Part A, 2011, v. 155A, n. 3, p. 642, doi. 10.1002/ajmg.a.33860
- By:
- Publication type:
- Article
De Novo Interstitial Deletion of 3q22.3-q25.2 Encompassing FOXL2, ATR, ZIC1, and ZIC4 in a Patient With Blepharophimosis/Ptosis/Epicanthus Inversus Syndrome, Dandy-Walker Malformation, and Global Developmental Delay.
- Published in:
- Journal of Child Neurology, 2011, v. 26, n. 5, p. 615, doi. 10.1177/0883073810384996
- By:
- Publication type:
- Article
Ontogeny of natural killer cells and T cells by analysis of BCR–ABL rearrangement from patients with chronic myelogenous leukaemia.
- Published in:
- British Journal of Haematology, 2000, v. 111, n. 1, p. 216, doi. 10.1046/j.1365-2141.2000.02341.x
- By:
- Publication type:
- Article
Diverse Genetic Landscape of Suspected Retinitis Pigmentosa in a Large Korean Cohort.
- Published in:
- Genes, 2021, v. 12, n. 5, p. 675, doi. 10.3390/genes12050675
- By:
- Publication type:
- Article
Genetic Profile and Associated Characteristics of 150 Korean Patients with Retinitis Pigmentosa.
- Published in:
- Journal of Ophthalmology, 2021, p. 1, doi. 10.1155/2021/5067271
- By:
- Publication type:
- Article