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- Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa
- 464 Phenotypic heterogeneity of epidermolysis bullosa associated with the recurrent pathogenic variant p.(Arg2000Trp) in plectin
- Pathogenesis and clinical features of alopecia in epidermolysis bullosa: A systematic review
- Inherited epidermolysis bullosa: clinical and therapeutic aspects
- Epidermolysis bullosa in animals: a review
- Dermatologia e Procedimentos Estéticos Ed. XXVII
- Líquen plano pilar e alopecia frontal fibrosante: correlação dos achados clínicos e dermatoscópicos com o grau de inflamação do exame histopatológico
- Avaliação do impacto da redução significativa de peso pela dieta cetogênica de muito baixa caloria nos parâmetros metabólicos, inflamatórios, hormonais e seminais de homens obesos
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- Dermatopathology and molecular genetics
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Alopecia in Epidermolysis Bullosa
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Research Techniques Made Simple: Zebrafish Models for Human Dermatologic Disease
- Epidermolysis Bullosa Simplex Caused by Distal Truncation of BPAG1-e: An Intermediate Generalized Phenotype with Prurigo Papules
- Epidermolysis Bullosa Simplex Keratinocytes Show Disturbed Mitochondrial Positioning and Activity
- Localized Epidermolysis Bullosa Simplex (Weber-Cockayne type)
- Keratin disorders: from gene to therapy
- Recessive Epidermolysis Bullosa Simplex Phenotype Reproduced in Vitro
- Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex
- Stem Cell Therapies for Epidermolysis Bullosa Treatment
- Characterization of the epidermal-dermal junction in hiPSC-derived skin organoids
- Assessment of Clients' Perceptions and Satisfaction With Eyebrow Mesotherapy Treatment
- Skin, Genetic Defects, and Aging
- DENOUEMENT—CONTINUED FROM P. 661
- Marine Health-Promoting Compounds: Recent Trends for Their Characterization and Human Applications
- Keratins and skin disease