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- Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa
- Inherited epidermolysis bullosa: clinical and therapeutic aspects
- Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review
- Alopecia in Epidermolysis Bullosa
- Stem Cell Therapies for Epidermolysis Bullosa Treatment
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- Oral Presentations
- The dental needs of children with Epidermolysis Bullosa and service delivery: a scoping review
- Evaluation of Clinical and Oral Findings in Patients with Epidermolysis bullosa
- Identification of a novel homozygous LAMB3 mutation in a Chinese male with junctional epidermolysis bullosa and severe urethra stenosis: A case report
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