[1] |
JI Xiaolu, LIU Jiaojiao, WANG Chunyan, CHEN Jing, FANG Xiaoyan, SHEN Qian, WANG Xiang, XU Hong.
Primary hyperoxaluria type 3 in 8 children: A case series report and literature review
[J]. Chinese Journal of Evidence-Based Pediatrics, 2022, 17(3): 230-234.
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[2] |
XU Xiaolin, HAN Tongxin, CHENG Xiaoling, WANG Xiaoling, MAO Huawei.
Analysis of the fluctuation of blood concentration in children using sirolimus: A case report
[J]. Chinese Journal of Evidence-Based Pediatrics, 2022, 17(3): 235-239.
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[3] |
CHEN Bin, DONG Xinran, WANG Huijun, WU Bingbing, YANG Lin, WANG Xiao, WANG Yaqiong, NI Qi, LI Chuan, ZHOU Wenhao, LU Yulan .
Next generation sequencing data analysis pipeline of Children's Hospital of Fudan University and its clinical application
[J]. Chinese Journal of Evidence-Based Pediatrics, 2022, 17(3): 202-209.
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[4] |
YE Yuanzhen, MAI Jiahui, HU Zhanqi, CHEN Li, LIAO Jianxiang, DUAN Jing.
11 cases of children with epilepsy caused by 16p11.2 deletion: A case series report
[J]. Chinese Journal of Evidence-Based Pediatrics, 2022, 17(2): 144-148.
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[5] |
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[J]. Chinese Journal of Evidence-Based Pediatrics, 2022, 17(2): 155-158.
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[6] |
ZHANG Nan, DUAN Yanlong, ZHOU Chunju, JIN Ling, YANG Jing, HUANG Shuang, ZHANG Meng, ZHANG Yonghong.
6 cases of large B-cell lymphoma with IRF4 gene rearrangement in children:A case series report and literature review
[J]. Chinese Journal of Evidence-Based Pediatrics, 2022, 17(1): 70-74.
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[7] |
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[J]. Chinese Journal of Evidence-Based Pediatrics, 2022, 17(1): 75-78.
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[8] |
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[J]. Chinese Journal of Evidence-Based Pediatrics, 2021, 16(6): 427-430.
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[9] |
ZENG Xingying, WU Huaping, ZENG Miao , YU Xiongying , LIU Zhiqiang.
24 children with early stage progressive muscular dystrophy:A case series report
[J]. Chinese Journal of Evidence-Based Pediatrics, 2021, 16(5): 391-394.
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[10] |
ZHANG Jie, XIE Han, DENG Jiong, XU Han, LIU Xianyu, LIN Zehong, CHANG Xuting, WU Ye.
Perampanel in the treatment of children with drug-resistant epilepsy based on the follow-up of 6-month efficacy:A single-center prospective cohort study
[J]. Chinese Journal of Evidence-Based Pediatrics, 2021, 16(4): 269-274.
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[11] |
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[J]. Chinese Journal of Evidence-Based Pediatrics, 2021, 16(3): 249-251.
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[12] |
CHEN Xiaoqing, HU Liyuan, WANG Laishuan, CHENG Guoqiang, CAO Yun, CHEN Chao, WANG Huijun, ZHOU Wenhao, YANG Lin.
14 cases of Kabuki syndrome caused by KMT2D gene mutation in neonates: A case series report and literature review
[J]. Chinese Journal of Evidence-Based Pediatrics, 2021, 16(2): 136-140.
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[13] |
DENG Dongli, XIAO Feifan, WU Bingbing, SUN Weihua, YANG Lin, LU Wei, ZHOU Wenhao.
41 cases of infants with methylmalonic acidemia: A case series report
[J]. Chinese Journal of Evidence -Based Pediatric, 2020, 15(6): 459-462.
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[14] |
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[J]. Chinese Journal of Evidence -Based Pediatric, 2020, 15(6): 471-475.
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[15] |
LU Xiao-xiao, LU Chun-mei, WANG Lai-shuan, CHENG Guo-qiang, WANG Hui-jun, ZHOU Wen-hao, WU Bing-bing, YANG Lin, WANG Ji-mei.
Retrospective analysis of 28 Chinese newborns with epidermolysis bullosa caused by pathogenic variations of COL7A1 gene
[J]. Chinese Journal of Evidence -Based Pediatric, 2020, 15(3): 210-214.
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