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New HLA Nomenclature (2010) and Its Clinical Application in Koreans

Lee KW, Park MH

Human leukocyte antigen (HLA) gene region encodes a set of HLA molecules functioning critical roles in immune response. Each HLA gene locus shows extensive polymorphism with ever-increasing number of alleles....
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First Report of Brain Abscess Associated with Pseudozyma species in a Patient with Astrocytoma

Hwang S, Kim J, Yoon S, Cha Y, Kim M, Yong D, Chang JH, Jeong SH, Uh Y, Lee K

A yeast-like strain was isolated from the brain abscess of a patient diagnosed with astrocytoma. Morphological and molecular analysis on D1/D2 domain in the 26S rRNA gene and internal transcript...
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Constitutional Pericentric Inversion 9 in Korean Patients with Chronic Myelogenous Leukemia

Suh B, Song J, Kim J, Park TS, Choi JR

BACKGROUND: Although the pericentric inversion of chromosome 9, inv(9)(p11q13), is generally considered a normal variation, it is also associated with solid tumors and several hematologic malignancies such as biphenotypic acute...
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Discrepancy in Genotyping of Apolipoprotein E between Allele-Specific PCR and Fluorescence Resonance Energy Transfer or Sequencing

Park CH, Lee ST, Ki CS, Kim JW

The human apolipoprotein E (APOE) gene contains several single-nucleotide polymorphisms (SNPs) that are distributed across the gene. The genotype of the APOE gene has important implications as a risk factor...
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Comparative Measurement of FVIII Inhibitors in Hemophilia A Patients Using ELISA and the Bethesda Assay

Kim SY, Kang SY, Lee WI

Factor VIII inhibitors are produced during or after coagulation factor VIII (FVIII) therapy in hemophilia A patients. These inhibitors are usually detected by a modified Bethesda assay or an enzymelinked...
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A Case of Partial Trisomy 2p23-pter Syndrome with Trisomy 18p Due to a de novo Supernumerary Marker Chromosome

Lee JH, Cho HS, Lee ES, Jung BC

Partial trisomy 2p is a rare but relatively well-defined syndrome with distinctive clinical features, including marked psychomotor delay, dysmorphic face, and congenital heart disease. The phenotype of trisomy 18p is...
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Analysis of Acquired Resistance Genes in Stenotrophomonas maltophilia

Song JH, Sung JY, Kwon KC, Park JW, Cho HH, Shin SY, Ko YH, Kim JM, Shin KS, Koo SH

BACKGROUND: Stenotrophomonas maltophilia is a gram-negative bacillus and a nosocomial pathogen in immunocompromised patients. Trimethoprim/sulfamethoxazole (TMP/SMX) is the drug of choice for treating S. maltophilia infection; however, resistance to TMP/SMX...
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A Girl with 15q Overgrowth Syndrome and dup(15)(q24q26.3) that Included Telomeric Sequences

Gutierrez-Franco MdlA, Madariaga-Campos MdlL, Vasquez-Velasquez AI, Matute E, Guevara-Yanez R, Rivera H

Distal 15q trisomy or tetrasomy is associated with a characteristic phenotype that includes mild to moderate intellectual disability, abnormal behavior, speech impairment, overgrowth, hyperlaxity, long face, prominent nose, puffy cheeks,...
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Clinical Characteristics and ALB Gene Mutation Analysis of Korean Patients with Bisalbuminemia

Kim YH, Lee YW, Jeon BR, Lee YK, Shin HB, Kang DH, Park SK, Hong DS, Lee ST, Kim JW, Ki CS

BACKGROUND: Bisalbuminemia is a hereditary or an acquired condition characterized by the presence of 2 albumin variants with different mobilities on serum protein electrophoresis (SPE). The clinical significance of bisalbuminemia...
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A Rare Case of Acute Lymphoblastic Leukemia with t(12;17)(p13;q21)

Kim JE, Woo KS, Kim KE, Kim SH, Park JI, Shaffer LG, Han JY

Patients with ALL rarely present with t(12;17)(p13;q21) as the primary clonal abnormality; this abnormality is associated with the expression of myeloid antigens. In this study, we have reported presumably the...
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Bone Marrow Cellularity Measurement by Myelocrit

Chang J, Park H, Chae H, Kim M, Kim Y, Han K

BACKGROUND: The bone marrow (BM) cellularity has been used as a major index for the evaluation of hematologic diseases and malignancies. However, the microscopic evaluation lacks objectivity because of considerable...
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Acquired Amegakaryocytic Thrombocytopenia after Thymectomy in a Case of Pure Red Cell Aplasia Associated with Thymoma

Cho AR, Cha YJ, Kim HR, Park EK, Cha EJ

The association of thymoma with pure red cell aplasia has been well documented, but amegakaryocytic thrombocytopenia is not a recognized paraneoplastic syndrome complicating thymoma. We report a case of thymoma-complicated...
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Measurement of Inflammatory Cytokines in Patients with Rheumatoid Arthritis

Kang SY, Kim MH, Lee WI

BACKGROUND: Inflammatory cytokines such as tumor necrosis factor alpha (TNFalpha) and interleukin (IL)-6 play an important role in pathophysiology of rheumatoid arthritis (RA). We investigated the possibility whether TNFalpha and...
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Comparison of R-mix Virus Culture and Multiplex Reverse Transcriptase-PCR for the Rapid Detection of Respiratory Viruses

Lim G, Park TS, Suh JT, Lee HJ

BACKGROUND: Respiratory viral infections can become epidemic due to high contagiosity. Since there was no rapid diagnostic method for complete diagnosis in the past, diagnosis was solely made on the...
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Clinical Relevance of Time-to-positivity in BACTEC9240 Blood Culture System

Park SH, Shim H, Yoon NS, Kim MN

BACKGROUND: Continuous monitoring systems have allowed determination of the time-to-positivity (TTP). We evaluated the clinical relevance of TTP in the BACTEC9240 system (Becton-Dickinson, USA). METHODS: A total of 2,354 vials...
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Diamond-Blackfan Anemia Confirmed by RPS19 Gene Mutation Analysis: A Case Study and Literature Review of Korean Patients

Chae H, Park J, Kim M, Lim J, Kim Y, Han K, Lee J, Chung NG, Cho B, Kim HK

Diamond-Blackfan anemia (DBA) is a rare congenital erythroid hypoplastic anemia that usually presents early in infancy and is inherited in up to 45% of cases. It is characterized by red...
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Clinical Importance of Morphological Multilineage Dysplasia in Acute Myeloid Leukemia with Myelodysplasia Related Changes

Park SH, Chi HS, Park SJ, Jang S, Park CJ

BACKGROUND: AML with myelodysplasia related changes (AML MRC) is known to show a poor prognosis compared with de novo AML, but controversies exist about the prognostic impact of multilineage dysplasia...
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A Case of Therapy-related ALL with MLL Gene Rearrangement Following Treatment of Breast Cancer

Cho J, Hur M, Moon HW, Yun YM, Lee CH, Lee HG

ALL with MLL gene rearrangement secondary to chemotherapy has been rarely reported. We report a case of therapy-related ALL (t-ALL) with MLL gene rearrangement in a patient who had undergone...
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Comparison of Blood Glucose Measurements Using Samples Obtained from the Forearm, Finger Skin Puncture, and Venous Serum

Park KS, Park MS, Cha YJ, Kim WJ, Choi SS, Kim KO, Cha EJ, Kim KA

BACKGROUND: Blood glucose testing (BGT) at the forearm minimizes the pain experienced during sampling of capillary blood. We compared the BGT results for forearm sampling with those for standard finger...
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