Xingyuan Jiang

发表

Effect of Methylene Blue on White Matter Injury after Ischemic Stroke

Weiguang Zhang, Chunhua Chen, Quancheng Cheng, 2021, Oxidative medicine and cellular longevity.

Bi-allelic Variants in LSS Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2.

Mao-ying Lin, Zhimiao Lin, Mingyang Lee, 2022, The Journal of investigative dermatology.

Two cases of Chanarin‐Dorfman syndrome with novel and recurrent mutations in the ABHD5 gene

Zhimiao Lin, Huijun Wang, Bo Yu, 2021, International journal of dermatology.

Somatic frameshift mutation in PIK3CA causes CLOVES syndrome by provoking PI3K/AKT/mTOR pathway

Wen Qin, Lin Ma, Zhimiao Lin, 2021, Hereditas.

Differential Diagnostic Models Between Vasovagal Syncope and Psychogenic Pseudosyncope in Children

Junbao Du, Selena Y. Chen, C. Tao, 2020, Frontiers in Neurology.

Variants in KLK11, affecting signal peptide cleavage of kallikrein-related peptidase 11, cause an autosomal-dominant cornification disorder.

Zhimiao Lin, Mingyang Lee, Huijun Wang, 2022, The British journal of dermatology.

Epidermolysis Bullosa Pruriginosa Treated With Baricitinib.

Zhimiao Lin, Mingyang Lee, Huijun Wang, 2021, JAMA dermatology.

Biallelic mutations in LSS in autosomal‐recessive mutilating palmoplantar keratoderma

Shengru Zhou, Zhimiao Lin, Xingyuan Jiang, 2023, Experimental dermatology.

Narrowing the Genomic Region of Autosomal-Dominant Congenital Generalized Hypertrichosis Terminalis.

Zhe Xu, Zhimiao Lin, Huijun Wang, 2021, JAMA dermatology.

Incompletely penetrant TRPM4‐associated progressive symmetric erythrokeratodermia responses to methotrexate

Zhimiao Lin, Huijun Wang, Xingyuan Jiang, 2022, The Journal of dermatology.