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Research 31–60 of 1000+
- Pathogenesis and clinical features of alopecia in epidermolysis bullosa: A systematic review
- Recently Identified Forms of Epidermolysis Bullosa
- Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa
- Inherited epidermolysis bullosa: clinical and therapeutic aspects
- Identification of a novel homozygous LAMB3 mutation in a Chinese male with junctional epidermolysis bullosa and severe urethra stenosis: A case report
- Poster presentationsSG11 KRT14 pathogenic or likely pathogenic variants beyond epidermolysis bullosa: dermatopathia pigmentosa reticularis
- The importance and use of stem cells in dermatology
- Dermatopathology and molecular genetics
- Keratin disorders: from gene to therapy
- Generalized atrophic benign epidermolysis bullosa.
- Oral Presentations
- Alopecia in Epidermolysis Bullosa
- Read-Through for Nonsense Mutations in Type XVII Collagen‒Deficient Junctional Epidermolysis Bullosa
- Focal palmoplantar callosities in non-Herlitz junctional epidermolysis bullosa
- Stem Cell Therapies for Epidermolysis Bullosa Treatment
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- The dental needs of children with Epidermolysis Bullosa and service delivery: a scoping review
- Junctional Epidermolysis Bullosa, Generalized Intermediate Type
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- Evaluation of Clinical and Oral Findings in Patients with Epidermolysis bullosa
- Epidermolysis Bullosa Simplex Caused by Distal Truncation of BPAG1-e: An Intermediate Generalized Phenotype with Prurigo Papules
- Hair Loss in Autoimmune Cutaneous Bullous Disorders
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- The Genetics of Human Skin Disease
- Advances in skin grafting and treatment of cutaneous wounds
- Life before and beyond blistering: The role of collagen XVII in epidermal physiology
- Keratin gene mutations in disorders of human skin and its appendages
- Characterization of the epidermal-dermal junction in hiPSC-derived skin organoids
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Hair follicle stem cell progeny heal blisters while pausing skin development