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Research 31–60 of 758
- Epidermolysis Bullosa
- 304 Sephardic Ancestry in Recessive Dystrophic Epidermolysis Bullosa Individuals Carrying the Prevalent c.6527insC Mutation
- Efficacy of a topical formulation of Henna (Lawsonia inermis) on the itch and wound healing in patients with epidermolysis bullosa: A pilot single-arm clinical trial
- 494 Epidermolysis bullosa pruriginosa, muscular dystrophy, and immune-mediated myasthenia gravis in a patient with homozygous nonsense PLEC mutation
- Inherited Epidermolysis Bullosa: A Clinical Case
- Epidermolysis Bullosa Acquisita Occuring In A Patient With Systemic Lupus Erythematosus
- 603 Pathological modeling of epidermolysis bullosa simplex (EBS) using induced pluripotent stem cells (iPSC)
- Pathogenesis and clinical features of alopecia in epidermolysis bullosa: A systematic review
- Epidermolysis bullosa in calves in the United Kingdom
- Systematized Epidermal Nevus with Epidermolytic Hyperkeratosis Improving with Topical Calcipotriol/Betametasone Dipropionate Combination Ointment
- Missense mutation Y449H of the K10 gene in a patient with severe epidermolytic ichthyosis
- Case of epidermolytic ichthyosis (bullous congenial ichthyosiform erythroderma) with a novel L157P mutation in KRT10 complicated by hypercalcemia
- Generalized atrophic benign epidermolysis bullosa.
- Read-Through for Nonsense Mutations in Type XVII Collagen‒Deficient Junctional Epidermolysis Bullosa
- P‐35 Nonlethal junctional epidermolysis bullosa in a dog
- 0873 Modeling junctional epidermolysis bullosa using tissue-engineered skin substitutes
- A homozygous nonsense mutation identified in <i>COL7A1</i> in a family with autosomal recessive dystrophic epidermolysis bullosa
- LB918 Analysis of National Inpatient Sample to characterize admissions for pediatric patients with dystrophic epidermolysis bullosa
- 302 Availability of mRNA Obtained from Peripheral Blood Mononuclear Cells for Mutational Analysis in Dystrophic Epidermolysis Bullosa
- Identification of a novel homozygous LAMB3 mutation in a Chinese male with junctional epidermolysis bullosa and severe urethra stenosis: A case report
- Junctional Epidermolysis Bullosa, Generalized Intermediate Type
- Localized Epidermolysis Bullosa Simplex (Weber-Cockayne type)
- Dominant dystrophic epidermolysis bullosa: Seven familial cases
- Superficial Epidermolytic Ichthyosis—Hypertrichosis as a Clue to Diagnosis
- No Evidence That Human Papillomavirus Is Responsible for the Aggressive Nature of Recessive Dystrophic Epidermolysis Bullosa–Associated Squamous Cell Carcinoma
- 519 Phase I/IIa clinical trial for recessive dystrophic epidermolysis bullosa using genetically corrected autologous keratinocytes
- Focal palmoplantar callosities in non-Herlitz junctional epidermolysis bullosa
- CRISPR/Cas9-Mediated Generation of <i>COL7A1</i>-Deficient Keratinocyte Model of Recessive Dystrophic Epidermolysis Bullosa.
- 572 Defining chronic wound types in recessive dystrophic epidermolysis bullosa patients for clinical outcome assessment
- Histological and molecular restoration of type VII collagen in Recessive dystrophic epidermolysis bullosa mouse skin by topical injection of keratinocyte-like cells differentiated from human adipose-derived mesenchymal stromal cells