Yoo Sukdong相关文献与解析，生知库 | 链接生命科学的每一步

Yoo, Sukdong; Kim, Kihun; Son, Eunjeong; Song, Tae-Jin; Kim, Hyun-Woo; Shin, Kihyuk; Ko, Dai Sik; Cho, Su-Yeon; Kwon, Yujin; Kim, Won Kyu; Kim, Yun Hak

癫痫

神经科学

发表日期：2026

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Allogenic mitochondria transfer improves cardiac function in iPS-cell-differentiated cardiomyocytes of a patient with Barth syndrome.

异体线粒体移植改善巴特综合征患者 iPS 细胞分化的心肌细胞的心脏功能

期刊:Experimental and Molecular Medicine

影响因子:12.9

doi:10.1038/s12276-025-01472-7

Kim Ye Seul, Yoo Sukdong, Jung Yoon Ji, Yoon Jung Won, Kwon Yong Seong, Lee Nayeon, Cheon Chong Kun, Kim Jae Ho

Comparison of growth hormone therapy response according to the presence of growth hormone deficiency in children born small for gestational age with short stature in Korea: a retrospective cohort study

韩国出生时胎龄偏小且身材矮小的儿童，根据是否存在生长激素缺乏症比较生长激素治疗反应：一项回顾性队列研究

期刊:BMC Pediatrics

影响因子:2

doi:10.1186/s12887-024-05339-0

Jo, Ha Young; Jang, Hyun Ji; Cheon, Chong Kun; Yoon, Ju Young; Yoo, Sukdong; Lee, Jung Hyun; Lee, Jeong Eun; Kim, Ye Jin; Kim, Sejin; Kim, Hyun-Ji; Choi, Im Jeong; Kwak, Min Jung

免疫/内分泌

发表日期：2025

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Global prevalence of autoimmune diseases in turner syndrome: a systematic review and meta-analysis

特纳综合征患者自身免疫性疾病的全球患病率：系统评价和荟萃分析

期刊:

影响因子:

doi:10.1080/07853890.2025.2573143

Hwang, Seongbeen; Park, Yonghee; Moon, Hyunoh; Kim, Kihun; Yoo, Sukdong; Cho, Su-Yeon; Kwon, Yujin; Kim, Won Kyu; Kim, Yun Hak

Identification of a novel mutation of the SHOX gene in a patient with Leri-Weill dyschondrosteosis accompanied by growth hormone deficiency

在一名患有 Leri-Weill 软骨发育不良并伴有生长激素缺乏症的患者中，鉴定出一种新的 SHOX 基因突变。

期刊:Annals of Pediatric Endocrinology & Metabolism

影响因子:3.3

doi:10.6065/apem.2346236.118

Kang, Jaebeen; Kim, Min-Ji; Yoo, Sukdong; Cheon, Chong Kun

A novel compound heterozygous variant of the COL11A1 gene in a patient with fibrochondrogenesis type I: the first case in Korea

韩国首例I型纤维软骨发育不全患者携带COL11A1基因新型复合杂合变异体

期刊:Annals of Pediatric Endocrinology & Metabolism

影响因子:3.3

doi:10.6065/apem.2346150.075

Jeon, Jaesung; Kim, Minji; Yoo, Sukdong; Kim, Yoomi; Cheon, Chong Kun

The impacts of COVID-19 on childhood obesity: prevalence, contributing factors, and implications for management

COVID-19 对儿童肥胖的影响：患病率、影响因素及管理启示

期刊:Annals of Pediatric Endocrinology & Metabolism

影响因子:3.3

doi:10.6065/apem.2346094.047

Kim, Min-Ji; Kim, Minji; Yoon, Ju Young; Cheon, Chong Kun; Yoo, Sukdong

The first case of novel variants of the FSHR mutation causing primary amenorrhea in 2 siblings in Korea

韩国首例由FSHR基因突变新变异体引起的原发性闭经病例报告，两名姐妹均来自韩国

期刊:Annals of Pediatric Endocrinology & Metabolism

影响因子:3.3

doi:10.6065/apem.2142116.058

Yoo, Sukdong; Yoon, Ju Young; Keum, Changwon; Cheon, Chong Kun

FSH

发表日期：2023

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Clinical relevance of targeted exome sequencing in patients with rare syndromic short stature

靶向外显子组测序在罕见综合征性矮小症患者中的临床意义

期刊:Orphanet Journal of Rare Diseases

影响因子:3.5

doi:10.1186/s13023-021-01937-8

Kamil, Gilyazetdinov; Yoon, Ju Young; Yoo, Sukdong; Cheon, Chong Kun

发表日期：2021

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Maternal smoking during pregnancy and childhood seizure: a systematic review and meta-analysis

孕期母亲吸烟与儿童癫痫：系统评价和荟萃分析

Allogenic mitochondria transfer improves cardiac function in iPS-cell-differentiated cardiomyocytes of a patient with Barth syndrome.

异体线粒体移植改善巴特综合征患者 iPS 细胞分化的心肌细胞的心脏功能

Comparison of growth hormone therapy response according to the presence of growth hormone deficiency in children born small for gestational age with short stature in Korea: a retrospective cohort study

韩国出生时胎龄偏小且身材矮小的儿童，根据是否存在生长激素缺乏症比较生长激素治疗反应：一项回顾性队列研究

Global prevalence of autoimmune diseases in turner syndrome: a systematic review and meta-analysis

特纳综合征患者自身免疫性疾病的全球患病率：系统评价和荟萃分析

Identification of a novel mutation of the SHOX gene in a patient with Leri-Weill dyschondrosteosis accompanied by growth hormone deficiency

在一名患有 Leri-Weill 软骨发育不良并伴有生长激素缺乏症的患者中，鉴定出一种新的 SHOX 基因突变。

A novel compound heterozygous variant of the COL11A1 gene in a patient with fibrochondrogenesis type I: the first case in Korea

韩国首例I型纤维软骨发育不全患者携带COL11A1基因新型复合杂合变异体

The impacts of COVID-19 on childhood obesity: prevalence, contributing factors, and implications for management

COVID-19 对儿童肥胖的影响：患病率、影响因素及管理启示

The first case of novel variants of the FSHR mutation causing primary amenorrhea in 2 siblings in Korea

韩国首例由FSHR基因突变新变异体引起的原发性闭经病例报告，两名姐妹均来自韩国

Clinical relevance of targeted exome sequencing in patients with rare syndromic short stature

靶向外显子组测序在罕见综合征性矮小症患者中的临床意义