日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

The Effect of Malnutrition, Inflammatory Biomarkers, and Stress-Induced Hyperglycemia on the Glomerular Filtration Rate in Renal Dysfunction

营养不良、炎症生物标志物和应激性高血糖对肾功能障碍患者肾小球滤过率的影响

Jang, Woori; Fujii, Noriyoshi; Fujii, Tatsuyoshi; Choi, Jong Weon

Case report: Development of central precocious puberty in a girl with late-diagnosed simple virilizing congenital adrenal hyperplasia complicated with Williams syndrome

病例报告:一名患有晚期诊断的单纯性男性化先天性肾上腺皮质增生症并合并威廉姆斯综合征的女孩出现中枢性性早熟

Joo, Eun Young; Yoo, Myung Ji; Kim, Su Jin; Jang, Woori; Lee, Ji-Eun

Clinical efficacy of multigene panels in the management of congenital hypothyroidism with gland in situ

多基因检测在原位甲状腺功能减退症治疗中的临床疗效

Park, Jisun; Joo, Eun Young; Yoo, Myung Ji; Kim, Su-Jin; Jang, Woori; Lee, Ji-Eun

Targeted Panel Sequencing Identifies an Intronic c.5225-3C>G Variant of the FBN1 Gene Causing Sporadic Marfan Syndrome with Annuloaortic Ectasia.

靶向测序发现 FBN1 基因内含子 c.5225-3C>G 变异导致散发性马凡综合征伴主动脉环扩张

Kim Kyung Hwa, Kim Tae Yun, Kim Soon Jin, Cho Yong Gon, Park Joonhong, Jang Woori

Potent synthetic and endogenous ligands for the adopted orphan nuclear receptor Nurr1

针对孤儿核受体 Nurr1 的有效合成和内源性配体

Yongwoo Jang, Woori Kim, Pierre Leblanc, Chun-Hyung Kim, Kwang-Soo Kim

A Neonate with Autosomal Dominant Pseudohypoaldosteronism Type 1 Due to a Novel Microdeletion of the NR3C2 Gene at 4q31.23

一名新生儿因 4q31.23 处 NR3C2 基因的新型微缺失而患有 1 型常染色体显性遗传性假性醛固酮增多症

Kim, Su Jin; Park, Dasom; Jang, Woori; Lee, Juyoung

Seroprevalence of Neutralizing Antibodies against Japanese Encephalitis Virus among Adolescents and Adults in Korea: A Prospective Multicenter Study

韩国青少年和成人中和日本脑炎病毒抗体血清阳性率:一项前瞻性多中心研究

Kwak, Byung Ok; Kwon, Young Se; Hong, Young Jin; Nahm, Chung Hyun; Jang, Woori; Uh, Young; Cho, Yong Gon; Kim, Jimyung; Kim, Myungshin; Kim, Dong Hyun

Cytokine clusters as potential diagnostic markers of disease activity and renal involvement in systemic lupus erythematosus

细胞因子簇作为系统性红斑狼疮疾病活动性和肾脏受累的潜在诊断标志物

Park, Joonhong; Jang, Woori; Park, Hye Sun; Park, Ki Hyun; Kwok, Seung-Ki; Park, Sung-Hwan; Oh, Eun-Jee

CDKN2B downregulation and other genetic characteristics in T-acute lymphoblastic leukemia

T细胞急性淋巴细胞白血病中CDKN2B下调及其他遗传特征

Jang, Woori; Park, Joonhong; Kwon, Ahlm; Choi, Hayoung; Kim, Jiyeon; Lee, Gun Dong; Han, Eunhee; Jekarl, Dong Wook; Chae, Hyojin; Han, Kyungja; Yoon, Jae-Ho; Lee, Seok; Chung, Nack-Gyun; Cho, Bin; Kim, Myungshin; Kim, Yonggoo

Chromosomal Microarray Analysis as a First-Tier Clinical Diagnostic Test in Patients With Developmental Delay/Intellectual Disability, Autism Spectrum Disorders, and Multiple Congenital Anomalies: A Prospective Multicenter Study in Korea

染色体微阵列分析作为发育迟缓/智力障碍、自闭症谱系障碍和多发性先天性异常患者的一线临床诊断检测:一项韩国前瞻性多中心研究

Jang, Woori; Kim, Yonggoo; Han, Eunhee; Park, Joonhong; Chae, Hyojin; Kwon, Ahlm; Choi, Hayoung; Kim, Jiyeon; Son, Jung Ok; Lee, Sang Jee; Hong, Bo Young; Jang, Dae Hyun; Han, Ji Yoon; Lee, Jung Hyun; Kim, So Young; Lee, In Goo; Sung, In Kyung; Moon, Yeonsook; Kim, Myungshin; Park, Joo Hyun