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Research 211–240 of 775
- 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
- Localized Epidermolysis Bullosa Simplex (Weber-Cockayne type)
- 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
- Dominant dystrophic epidermolysis bullosa: Seven familial cases
- Focal palmoplantar callosities in non-Herlitz junctional epidermolysis bullosa
- 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
- 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
- 312 CRISPR/Cas9-based targeted genome editing for correction of recessive dystrophic epidermolysis bullosa using iPS cells
- Case of non-Herlitz junctional epidermolysis bullosa with<i>COL17A1</i>mutation
- Scarring Alopecia in Localized Dystrophic Epidermolysis Bullosa: A Case Report and a Scoping Review
- 454 Modeling epidermolysis bullosa simplex with cardiomyopathy using KLHL24-mutant pluripotent stem cells.
- Localized variant of junctional epidermolysis bullosa with R795X mutation
- 259 Scalp hair follicle dermal sheath fibroblasts express genes associated with promotion of skin integrity/wound healing and prevention of autoimmune responses in Recessive Dystrophic Epidermolysis Bullosa
- Antiviral drugs prolong survival in murine recessive dystrophic epidermolysis bullosa