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- Hair follicle stem cell progeny heal blisters while pausing skin development
- Hair follicle stem cell progeny heal blisters while pausing skin development
- Skin fragility, diffuse ecchymosis and blisters on a yellowish waxy base
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- Mechanical forces in skin disorders
- A newborn presenting with congenital blistering
- A blistering child: sudden erythema with blisters in a sick girl
- Faculty Opinions recommendation of Loss of desmocollin 3 in mice leads to epidermal blistering.
- The role of Kindlin-1 in skin homeostasis and tumor development
- The role of natural killer cells in autoimmune blistering diseases
- A case of antilaminin 332 mucous membrane pemphigoid showing a blister on the bulbar conjunctiva and a unique epitope on the α3 subunit
- A Neonate with Blisters
- Skin disorders in Parkinson’s disease: potential biomarkers and risk factors
- KERATINS AND SKIN DISORDERS
- Congenital and Hereditary Skin Diseases
- Skin, Genetic Defects, and Aging
- 3D organotypic skin models recapitulate autoantibody-driven pemphigus pathomechanisms and targeted therapeutic response
- 606 The role of diet in patients with autoimmune blistering disease: A survey of the International Pemphigus and Pemphigoid Foundation
- Patient satisfaction and complications following laser hair removal in ethnic skin
- PATTERN OF SKIN DISEASES IN GERIATRIC PATIENTS ATTENDING TERTIARY CARE CENTRE
- Granzyme B in Autoimmune Skin Disease
- Inherited epidermolysis bullosa: clinical and therapeutic aspects
- Subcutaneous emphysema resulting from liquid nitrogen spray
- Laminin 332 Is Indispensable for Homeostatic Epidermal Differentiation Programs
- A Novel In Vivo Active Pemphigus Model Targeting Desmoglein1 and Desmoglein3: A Tool Representing All Pemphigus Variants
- IgG/IgA pemphigus with differing regional presentations
- Hemidesmosomes and Notch signaling regulate epidermal differentiation via delamination
- EBS in Children with De Novo Pathogenic Variants Disturbing Krt14
- Classic Sweet sydrome: A case report
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report