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Research 241–270 of 747
- Loose anagen hair syndrome in two patients with epidermolysis bullosa simplex, Dowling-Meara type
- Scarring alopecia and nail loss in a patient with epidermolysis bullosa acquisita
- Evaluation of Clinical and Oral Findings in Patients with Epidermolysis bullosa
- Diffuse partial woolly hair in a patient with epidermolysis bullosa simplex with mottled pigmentation
- 84: Cannabinoid use for symptom management in epidermolysis bullosa
- 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
- 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
- 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
- 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
- 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