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Direct LDL Cholesterol Assay vs. Estimated Equations in Patients With Hypertriglyceridemia or Low LDL Cholesterol Levels

Rodríguez-Domínguez J, Piedra-Aguilera , Martínez-Bujidos M, Malumbres-Serrano S, Morales-Indiano C, Fernández-Prendes C

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A Severe Infection Caused by a White Colony-Producing Strain of Clostridioides difficile RTC41/ST588

Park SY, Kim H, Lee Y

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Usefulness of Component-Resolved Diagnosis of Pollen-Food Allergy Syndrome

Lee MW, Lee HJ, Moon S, Shin KH

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The First Case of Pulmonary Mucormycosis Caused by Lichtheimia ornata

Lee J, Lee DG, Lee R, Yoon JH, Beck KS, Yoo IY, Park YJ

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Detection of a High-Dose Hook Effect and Evaluation of Dilutions of Urine Myoglobin Specimens Using a Serum Myoglobin Assay

Hunsaker JJH, La’ulu SL, Zupan E, Patel D, Pandya V, Rudolf JW

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Comparative Analysis of AB vs. ABO-specific Plasma for Desensitization in Blood Group O Recipients: An In Vitro Study

Lim YA

Neutralizing capacity measurement (NCM) of soluble ABH substances (SAS) in plasma was assessed to guide the selection of the appropriate ABO group of fresh-frozen plasma (FFP) for plasma exchange (PE)...
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Comparison of Measurable Residual Disease in Pediatric B-Lymphoblastic Leukemia Using Multiparametric Flow Cytometry and Next-Generation Sequencing

Hwang SM, Oh I, Kwon SR, Lee JS, Seong MW

Measurable residual disease (MRD) testing, a standard procedure in B-lymphoblastic leukemia (B-ALL) diagnostics, is assessed using multiparametric flow cytometry (MFC) and next-generation sequencing (NGS) analysis of immunoglobulin gene rearrangements. We...
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NUP214 Rearrangements in Leukemia Patients: A Case Series From a Single Institution

Choi YJ, Min YK, Lee ST, Choi JR, Shin S

Background: The three best-known NUP214 rearrangements found in leukemia (SET:: NUP214, NUP214::ABL1, and DEK::NUP214) are associated with treatment resistance and poor prognosis. Mouse experiments have shown that NUP214 rearrangements alone are...
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Guide to Rho(D) Immune Globulin in Women With Molecularly Defined Asian-type DEL (c.1227G>A)

Jeong IH, Yu S, Kim TY, Oh SY, Cho D

Rh hemolytic disease of the fetus and newborn is a potential risk for D-negative mothers who produce anti-D during pregnancy, which can lead to morbidity and mortality in subsequent pregnancies....
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TSHR Variant Screening and Phenotype Analysis in 367 Chinese Patients With Congenital Hypothyroidism

Zhang HY, Wu FY, Li XS, Tu PH, Zhang CX, Yang RM, Cui RJ, Wu CY, Fang Y, Yang L, Song HD, Zhao SX

Background: Genetic defects in the human thyroid-stimulating hormone (TSH) receptor (TSHR) gene can cause congenital hypothyroidism (CH). However, the biological functions and comprehensive genotype–phenotype relationships for most TSHR variants associated...
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Manufacturing Cell and Gene Therapies: Challenges in Clinical Translation

Lee NK, Chang JW

The safety and efficacy of both cell and gene therapies have been demonstrated in numerous preclinical and clinical trials. Chimeric antigen receptor T (CAR-T) cell therapy, which leverages the technologies...
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Comparison of Optical Genome Mapping With Conventional Diagnostic Methods for Structural Variant Detection in Hematologic Malignancies

Shim Y, Koo YK, Shin S, Lee ST, Lee KA, Choi JR

Background: Structural variants (SVs) are currently analyzed using a combination of conventional methods; however, this approach has limitations. Optical genome mapping (OGM), an emerging technology for detecting SVs using a...
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