Zhe Xu

发表

Dermoscopy of papular elastorrhexis

Jia-Qing Zhao, Zhe Xu, Bin Wang, 2021, Chinese medical journal.

Characterization of community-associated Staphylococcus aureus from skin and soft-tissue infections: a multicenter study in China

Y. Liu, Zhe Xu, Zhou Yang, 2016, Emerging Microbes & Infections.

Germline Mutation of PLCD1 Contributes to Human Multiple Pilomatricomas through Protein Kinase D/Extracellular Signal–Regulated Kinase1/2 Cascade and TRPV6

P. Yi, X. Zhang, Luoying Zhang, 2020 .

Novel pathogenic variants in the RECQL4 gene causing Rothmund‐Thomson syndrome in three Chinese patients

Zhe Xu, Wen Qin, Zhimiao Lin, 2021, The Journal of dermatology.

A Case of Hailey–Hailey Disease in an Infant with a New ATP2C1 Gene Mutation

Li Li, Zhe Xu, Lin Ma, 2011, Pediatric dermatology.

Heterozygous somatic activating AKT1 mutation in a case of Proteus syndrome with mental retardation

Zhe Xu, Lin Ma, Yu-juan Sun, 2014, The Journal of dermatology.

Calcification of the placenta in a woman with pseudoxanthoma elasticum with a mutation of the ABCC 6 gene

Zhe Xu, Lin Ma, Yu-juan Sun, 2014 .

Mycobacterium smegmatis in Skin Biopsy Specimens from Patients with Suppurative Granulomatous Inflammation

Yi-Wei Tang, Zhe Xu, Xia Zhang, 2013, Journal of Clinical Microbiology.

Mycobacterium smegmatis in skin biopsies from patients with suppurative granulomatous

Yi-Wei Tang, Zhe Xu, Xia Zhang, 2013 .

Pitted Keratolysis, Erythrasma and Erysipeloid

Ying Liu, Zhe Xu, Lin Ma, 2019, Harper's Textbook of Pediatric Dermatology.

Sporadic onset of erythermalgia: A gain‐of‐function mutation in Nav1.7

A. M. Rush, S. Dib-Hajj, S. Waxman, 2006, Annals of neurology.

Congenital ichthyosiform erythroderma with a novel variant in ABCA12 in a Chinese patient

Zhan Qi, Zhe Xu, Lin Ma, 2020, Pediatric investigation.

Novel ABCA12 compound heterozygous mutations identified in a patient with congenital ichthyosiform erythroderma and aortopulmonary window

Zhe Xu, Lin Ma, H. Xing, 2019, European Journal of Dermatology.

DNA polymerase-α regulates type I interferon activation through cytosolic RNA:DNA synthesis

Nan Yan, A. Zinn, H. Mussaffi, 2016, Nature Immunology.

Generalized Pustular Psoriasis in Patients with Interferon Gamma (IFN-γ) Receptor Deficiency and Mycobacterial Infection

Jinrong Liu, Shunying Zhao, Zhe Xu, 2021, Journal of Clinical Immunology.

Hutchinson–Gilford Progeria Syndrome Caused by an LMNA Mutation: A Case Report

Zhe Xu, Lin Ma, Zigang Xu, 2015, Pediatric dermatology.

Detection of mycobacterial and viral DNA in Kikuchi-Fujimoto disease: an analysis of 153 Chinese pediatric cases

Ying Liu, Charles W. Stratton, C. Stratton, 2017, Science China Life Sciences.

Gain-of-Function Mutations in TRPM4 Activation Gate Cause Progressive Symmetric Erythrokeratodermia.

Jie Zheng, D. Bu, Zhe Xu, 2019, The Journal of investigative dermatology.

Large deletions in the NSDHL gene in two patients with CHILD syndrome.

B. Hartmann, R. Happle, J. Fischer, 2015, Acta Dermato-Venereologica.

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

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

Novel MBTPS2 mutation causes a mild phenotype of ichthyosis follicularis with atrichia and photophobia syndrome in a Chinese pedigree

Zhe Xu, Lin Ma, H. Xing, 2018, Journal of dermatology (Print).