Dowling-Meara Epidermolysis Bullosa Simplex Latest Advances
Find the Latest Research About Dowling-Meara Epidermolysis Bullosa Simplex
Last Updated: 04/28/2026
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Found 744 publications
Dupilumab Use in Severe Epidermolysis Bullosa Simplex.
Journal: JAMA dermatology
Published: February 25, 2026
Supraglottic and Glottic Involvement in Epidermolysis Bullosa Simplex: A Pediatric Case Report and Review of Airway Management.
Journal: Ear, nose, & throat journal
Published: January 27, 2026
Nail Dystrophy Treated With Marigold Therapy in a Patient With Epidermolysis Bullosa Simplex.
Journal: The Australasian journal of dermatology
Published: January 25, 2026
Genetic analysis of a Chinese pedigree affected with Epidermolysis bullosa simplex due to a novel variant of KRT5 gene
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: December 26, 2025
Treatment Landscape for Epidermolysis Bullosa Simplex: A Review of Established and Emerging Therapies.
Journal: Pediatric dermatology
Published: November 12, 2025
A novel variant c.A527G in ITGB4 leads to autosomal dominant epidermolysis bullosa in China.
Journal: Frontiers in medicine
Published: October 16, 2025
Development and Validation of a Scale to Assess Epidermolysis Bullosa Simplex Severity.
Journal: JAMA dermatology
Published: October 15, 2025
Neonatal KLHL24-Associated Epidermolysis Bullosa Simplex: Clinical Presentation and Genetic Confirmation of a Rare Skin Fragility Syndrome.
Journal: Pediatric dermatology
Published: August 11, 2025
The p.Asn176Ser Variant of KRT5 at the Heptad "e" Position of the Helix Initiation Motif Causes Severe Epidermolysis Bullosa Simplex.
Journal: The Journal of dermatology
Published: July 24, 2025
Last Updated: 04/28/2026