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Research 30 of 776
- Skin disorders in Parkinson’s disease: potential biomarkers and risk factors
- PATTERN OF SKIN DISEASES IN GERIATRIC PATIENTS ATTENDING TERTIARY CARE CENTRE
- The role of natural killer cells in autoimmune blistering diseases
- Granzyme B in Autoimmune Skin Disease
- Congenital and Hereditary Skin Diseases
- 606 The role of diet in patients with autoimmune blistering disease: A survey of the International Pemphigus and Pemphigoid Foundation
- KERATINS AND SKIN DISORDERS
- Recognition and management of <i>Staphylococcus aureus</i> toxin‐mediated disease
- Cocaine-related bullous disease
- Hair follicle stem cell progeny heal blisters while pausing skin development
- Hair follicle stem cell progeny heal blisters while pausing skin development
- 464 Phenotypic heterogeneity of epidermolysis bullosa associated with the recurrent pathogenic variant p.(Arg2000Trp) in plectin
- A clinical study of geriatric dermatoses
- DEVELOPMENT OF A DESMOCOLLIN-3 ACTIVE MOUSE MODEL RECAPITULATING HUMAN ATYPICAL PEMPHIGUS
- Recently Identified Forms of Epidermolysis Bullosa
- Cutaneous manifestations associated with immune checkpoint inhibitors
- 010 Development of a Desmocollin-3 Active Mouse Model Recapitulating Human Atypical Pemphigus
- In this Issue
- 3D organotypic skin models recapitulate autoantibody-driven pemphigus pathomechanisms and targeted therapeutic response
- Mechanical forces in skin disorders
- Faculty Opinions recommendation of Loss of desmocollin 3 in mice leads to epidermal blistering.
- Skin Development and Disease: A Molecular Perspective
- A Novel In Vivo Active Pemphigus Model Targeting Desmoglein1 and Desmoglein3: A Tool Representing All Pemphigus Variants
- Mice lacking desmocollin 1 show epidermal fragility accompanied by barrier defects and abnormal differentiation
- Heterogeneous disease: A child case of lichen planus pemphigoides triggered by varicella
- Cutaneous Lesions in Systemic Lupus Erythematosus
- Abstracts
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- A case of antilaminin 332 mucous membrane pemphigoid showing a blister on the bulbar conjunctiva and a unique epitope on the α3 subunit
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report