- Manifestation and treatment in a cleidocranial dysplasia patient with a RUNX2 (T420I) mutation
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Lee C, Jung HS, Baek JA, Leem DH, Ko SO
- KMID: 2381867
- Maxillofac Plast Reconstr Surg.
- 2015 Nov;37(11):41.
- doi: 10.1186/s40902-015-0042-0
Cleidocranial dysplasia is an autosomal dominant heritable skeletal disorder. The characteristic features of cleidocranial dysplasia (CCD) may include hypoplasia of the clavicle, delayed closure of frontanelles, late tooth eruption, and... -
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- Diagnosis and Treatment of Pediatric Acute Myeloid Leukemia
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Lee JW, Cho B
- KMID: 2168914
- Clin Pediatr Hematol Oncol.
- 2015 Apr;22(1):8-14.
- doi: 10.15264/cpho.2015.22.1.8
Acute myeloid leukemia (AML) is a heterogeneous malignancy that comprises 25-30% of pediatric leukemias in Korea. Several inherited diseases, such as Down syndrome and Fanconi anemia, predispose towards AML leukemogenesis.... -
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- Incidences and Prognostic Impact of c-KIT, WT1, CEBPA, and CBL Mutations, and Mutations Associated With Epigenetic Modification in Core Binding Factor Acute Myeloid Leukemia: A Multicenter Study in a Korean Population
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Park SH, Lee HJ, Kim IS, Kang JE, Lee EY, Kim HJ, Kim YK, Won JH, Bang SM, Kim H, Song MK, Chung JS, Shin HJ
- KMID: 2363200
- Ann Lab Med.
- 2015 May;35(3):288-297.
- doi: 10.3343/alm.2015.35.3.288
BACKGROUND: To identify potential molecular prognostic markers in core binding factor (CBF) AML, we analyzed incidences and prognostic impacts of mutations in c-KIT, WT1, CEBPA, CBL, and a number of... -
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- Derivation and Differentiation of Bone Marrow Mesenchymal Stem Cells from Osteoarthritis Patients
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Gari M, Alsehli H, Gari A, Abbas M, Alkaff M, Abuzinadah M, Al-Sayes F, Gari M, Dallol A, Abuzenadah AM, Gauthaman
- KMID: 2360885
- Tissue Eng Regen Med.
- 2016 Dec;13(6):732-739.
- doi: 10.1007/s13770-016-0013-2
Osteoarthritis (OA) of the knee is a degenerative joint disease caused by the progressive reduction of the articular cartilage surface that leads to reduced joint function. Cartilage degeneration occurs through... -
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