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Research 61–90 of 1000+
- Granzyme B in Autoimmune Skin Disease
- KERATINS AND SKIN DISORDERS
- Treatment of alopecia areata with squaric acid dibutylester
- A clinical study of geriatric dermatoses
- The Role of Therapy in Impairing Quality of Life in Dermatological Patients: A Multinational Study
- Cutaneous manifestations associated with immune checkpoint inhibitors
- Patient satisfaction and complications following laser hair removal in ethnic skin
- Fixed-Drug Eruption due to Dextromethorphan
- Pigmented Hair-Thickening Fibers: A Camouflage Technique for Alopecia in Patients with Epidermolysis Bullosa
- PATTERN OF SKIN DISEASES IN GERIATRIC PATIENTS ATTENDING TERTIARY CARE CENTRE
- Severe Marking-Nut Dermatitis
- Diphenylcyclopropenone Treatment Outcomes for Alopecia Areata
- 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
- Case of non-Herlitz junctional epidermolysis bullosa with<i>COL17A1</i>mutation
- Clinical Considerations of Bioequivalence for Topical Dermatologic Drugs
- 464 Phenotypic heterogeneity of epidermolysis bullosa associated with the recurrent pathogenic variant p.(Arg2000Trp) in plectin
- 307 Phenotypic-genotypic expansion of plectinopathy in a patient with muscular dystrophy and immune-mediated myasthenia gravis
- 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
- Congenital and Hereditary Skin Diseases
- Skin, Genetic Defects, and Aging
- Mechanical forces in skin disorders
- Dermatosurgical techniques for repigmentation of vitiligo
- What's new in the pathogeneses and triggering factors of bullous pemphigoid
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- Superficial Epidermolytic Ichthyosis—Hypertrichosis as a Clue to Diagnosis
- IgG/IgA pemphigus with differing regional presentations
- Hemidesmosomes and Notch signaling regulate epidermal differentiation via delamination