Peiguang G. Wang
Hefei, China
Last Updated: 09/26/2026
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Found 18 publications
Serum levels of interleukin-17, -18, -22, and -25 in patients with bullous pemphigoid before and after treatment.
Journal: Frontiers in medicine
Published: January 12, 2025
Multitranscriptome analysis reveals stromal cells in the papillary dermis to promote angiogenesis in psoriasis vulgaris.
Journal: The British journal of dermatology
Published: July 02, 2024
The evaluation of Congo red staining combined with fluorescence microscopy in the diagnosis of primary cutaneous amyloidosis.
Journal: The Journal of dermatology
Published: April 24, 2024
Corrigendum: Case report: Challenges in the diagnosis of a case of Mal de Meleda and a therapeutic attempt of ixekizumab and Adalimumab.
Journal: Frontiers in medicine
Published: November 23, 2022
An intronic splice-site variant in MBTPS2 underlies ichthyosis follicularis with atrichia and photophobia syndrome.
Journal: The Journal of dermatology
Published: June 09, 2022
A novel mutation in SPINK5 gene underlies a case of atypical Netherton syndrome.
Journal: Frontiers in genetics
Published: May 13, 2022
Case Report: Chanarin-Dorfman Syndrome: A Novel Homozygous Mutation in ABHD5 Gene in a Chinese Case and Genotype-Phenotype Correlation Analysis.
Journal: Frontiers in genetics
Published: January 02, 2022
Case Report: Challenges in the Diagnosis of a Case of Mal de Meleda and a Therapeutic Attempt of Ixekizumab and Adalimumab.
Journal: Frontiers in medicine
Published: November 24, 2021
Case Report: A Case of Hailey-Hailey Disease Mimicking Condyloma Acuminatum and a Novel Splice-Site Mutation of ATP2C1 Gene.
Journal: Frontiers in genetics
Published: September 15, 2021
Annular epidermolytic ichthyosis with palmoplantar keratosis: a unique phenotype associated with interfamilial phenotypic heterogeneity.
Journal: European journal of dermatology : EJD
Published: July 16, 2020
Identification of a Novel Mutation in SASH1 Gene in a Chinese Family With Dyschromatosis Universalis Hereditaria and Genotype-Phenotype Correlation Analysis.
Journal: Frontiers in genetics
Published: April 28, 2020
Pathogenic EDA Mutations in Chinese Han Families With Hypohidrotic Ectodermal Dysplasia and Genotype-Phenotype: A Correlation Analysis.
Journal: Frontiers in genetics
Published: June 24, 2019
Last Updated: 09/26/2026