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Research 31–60 of 809
- Patient satisfaction and complications following laser hair removal in ethnic skin
- Hair follicle stem cell progeny heal blisters while pausing skin development
- A case of antilaminin 332 mucous membrane pemphigoid showing a blister on the bulbar conjunctiva and a unique epitope on the α3 subunit
- Pigmented Hair-Thickening Fibers: A Camouflage Technique for Alopecia in Patients with Epidermolysis Bullosa
- Focal palmoplantar callosities in non-Herlitz junctional epidermolysis bullosa
- Severe Marking-Nut Dermatitis
- PATTERN OF SKIN DISEASES IN GERIATRIC PATIENTS ATTENDING TERTIARY CARE CENTRE
- A Novel In Vivo Active Pemphigus Model Targeting Desmoglein1 and Desmoglein3: A Tool Representing All Pemphigus Variants
- Diphenylcyclopropenone Treatment Outcomes for Alopecia Areata
- Case of non-Herlitz junctional epidermolysis bullosa with<i>COL17A1</i>mutation
- 010 Development of a Desmocollin-3 Active Mouse Model Recapitulating Human Atypical Pemphigus
- DEVELOPMENT OF A DESMOCOLLIN-3 ACTIVE MOUSE MODEL RECAPITULATING HUMAN ATYPICAL PEMPHIGUS
- Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review
- Comparative trail on efficacy of topical contact immunotherapy with dinitrochlorobenzene and diphenylcyclopropenone in alopecia areata
- Pathogenesis and clinical features of alopecia in epidermolysis bullosa: A systematic review
- 577 Successful allogeneic epidermal grafting of chronic recessive dystrophic epidermolysis bullosa wounds from hematopoietic cell donors in the outpatient setting
- Skin, Genetic Defects, and Aging
- Znaczenie chorób pęcherzycowych w diagnostyce różnicowej estetycznych problemów twarzy
- 464 Phenotypic heterogeneity of epidermolysis bullosa associated with the recurrent pathogenic variant p.(Arg2000Trp) in plectin
- Acrodermatitis enteropathica – diagnostic challenges
- 307 Phenotypic-genotypic expansion of plectinopathy in a patient with muscular dystrophy and immune-mediated myasthenia gravis
- Congenital and Hereditary Skin Diseases
- Recognition and management of <i>Staphylococcus aureus</i> toxin‐mediated disease
- Mechanical forces in skin disorders
- What's new in the pathogeneses and triggering factors of bullous pemphigoid
- Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex
- Expression of MK6a dominant-negative and C-terminal mutant transgenes in mice has distinct phenotypic consequences in the epidermis and hair follicle
- Alopecia in Epidermolysis Bullosa
- Heterogeneous disease: A child case of lichen planus pemphigoides triggered by varicella
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report