Case report: Novel DGUOK variants associated with idiopathic non-cirrhotic portal hypertension in a Han Chinese child

por Li, Jia-Qi, Feng, Jia-Yan, Gong, Ying, Li, Wang-Qiang, Liu, Teng
Publicado 2023

Novel methionyl-tRNA synthetase gene variants/phenotypes in interstitial lung and liver disease: A case report and review of literature

por Abuduxikuer, Kuerbanjiang, Feng, Jia-Yan, Lu, Yi, Xie, Xin-Bao, Chen, Lian, Wang, Jian-She
Publicado 2018

A mutation in PIK3CD gene causing pediatric systemic lupus erythematosus: A case report

por Li, Guo-Min, Liu, Hai-Mei, Guan, Wan-Zhen, Xu, Hong, Wu, Bing-Bing, Feng, Jia-Yan, Sun, Li
Publicado 2019

A novel homozygous mutation in the glycerol-3-phosphate dehydrogenase 1 gene in a Chinese patient with transient infantile hypertriglyceridemia: a case report

por Li, Jia-Qi, Xie, Xin-Bao, Feng, Jia-Yan, Chen, Lian, Abuduxikuer, Kuerbanjiang, Lu, Yi, Li, Yu-Chuan, Wang, Jian-She
Publicado 2018

Neonatal Dubin-Johnson Syndrome and its Differentiation from Biliary Atresia

por Liu, Teng, Zhao, Jing, Feng, Jia-Yan, Lu, Yi, Sheps, Jonathan A., Wang, Ren-Xue, Han, Jun, Ling, Victor, Wang, Jian-She
Publicado 2023

Lupus podocytopathy and antiphospholipid syndrome in a child with SLE: A case report and literature review

por Li, Guo-min, Li, Yi-fan, Zeng, Qiao-qian, Zhang, Xiao-mei, Liu, Hai-mei, Feng, Jia-yan, Shi, Yu, Wu, Bing-bing, Xu, Hong, Sun, Li
Publicado 2022

Defects in myosin VB are associated with a spectrum of previously undiagnosed low γ‐glutamyltransferase cholestasis

por Qiu, Yi‐Ling, Gong, Jing‐Yu, Feng, Jia‐Yan, Wang, Ren‐Xue, Han, Jun, Liu, Teng, Lu, Yi, Li, Li‐Ting, Zhang, Mei‐Hong, Sheps, Jonathan A., Wang, Neng‐Li, Yan, Yan‐Yan, Li, Jia‐Qi, Chen, Lian, Borchers, Christoph H., Sipos, Bence, Knisely, A.S., Ling, Victor, Xing, Qing‐He, Wang, Jian‐She
Publicado 2017