Huan Xing
Beijing, China
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 16 publications
Off-label use of dupilumab in the management of pediatric urticaria vasculitis: A promising therapeutic choice.
Journal: Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology
Published: November 14, 2024
Consumer Preferences and Willingness to Pay for High-Quality Vegetable Oils: A Cross-Sectional Analysis of Chinese Residents.
Journal: Foods (Basel, Switzerland)
Published: March 11, 2024
Segmental hypopigmentation and unilateral fibrous patches: an unusual presentation of tuberous sclerosis complex with a novel TSC2 mutation.
Journal: International journal of dermatology
Published: June 26, 2023
Successful treatment of urticarial vasculitis with omalizumab in children: a case series.
Journal: Clinical and experimental dermatology
Published: January 22, 2023
Pityriasis versicolor on the scalp: An unusual distribution of a common disease.
Journal: Pediatric investigation
Published: November 11, 2022
Novel pathogenic variants in KIT gene in three Chinese piebaldism patients.
Journal: Frontiers in medicine
Published: September 09, 2022
Primary localized cutaneous amyloidosis presenting only as hypopigmented patches: A case report.
Journal: The Journal of dermatology
Published: January 12, 2022
Epidermodysplasia verruciformis mimicking pityriasis versicolor.
Journal: Pediatric investigation
Published: December 23, 2021
Multiple hypomelanotic macules in an infant cannot be ignored.
Journal: Pediatric investigation
Published: December 30, 2020
Facet-dependent decoration of TiO2 mesocrystals on TiO2 microcrystals for enhanced photoactivity.
Journal: Nanotechnology
Published: September 25, 2019
Novel ABCA12 compound heterozygous mutations identified in a patient with congenital ichthyosiform erythroderma and aortopulmonary window.
Journal: European journal of dermatology : EJD
Published: December 12, 2018
Novel MBTPS2 mutation causes a mild phenotype of ichthyosis follicularis with atrichia and photophobia syndrome in a Chinese pedigree.
Journal: The Journal of dermatology
Published: October 09, 2018
Last Updated: 09/26/2026