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Research 30 of 844
- 162 A review of the clinical and histopathological characteristics of patients with subepidermal blistering disorders presenting to a tertiary care centre in India
- KERATINS AND SKIN DISORDERS
- Skin disorders in Parkinson’s disease: potential biomarkers and risk factors
- Mechanical forces in skin disorders
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- 606 The role of diet in patients with autoimmune blistering disease: A survey of the International Pemphigus and Pemphigoid Foundation
- PATTERN OF SKIN DISEASES IN GERIATRIC PATIENTS ATTENDING TERTIARY CARE CENTRE
- Congenital and Hereditary Skin Diseases
- Care of the newborn with ichthyosis
- A clinical study of geriatric dermatoses
- 307 Phenotypic-genotypic expansion of plectinopathy in a patient with muscular dystrophy and immune-mediated myasthenia gravis
- Heterogeneous disease: A child case of lichen planus pemphigoides triggered by varicella
- Alopecia developed in a transitional case from pemphigus foliaceus to pemphigus vulgaris
- 3D organotypic skin models recapitulate autoantibody-driven pemphigus pathomechanisms and targeted therapeutic response
- Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex
- A Comprehensive Review on Trichogram and Trichoscopy in Dermatology
- Clinical Patterns and Frequency of Dermatological Manifestations Associated with Pregnancy
- A newborn presenting with congenital blistering
- A case of antilaminin 332 mucous membrane pemphigoid showing a blister on the bulbar conjunctiva and a unique epitope on the α3 subunit
- Abstracts
- The role of Kindlin-1 in skin homeostasis and tumor development
- Znaczenie chorób pęcherzycowych w diagnostyce różnicowej estetycznych problemów twarzy
- A blistering child: sudden erythema with blisters in a sick girl
- Keratin gene mutations in disorders of human skin and its appendages
- Role of nutritional supplements in selected dermatological disorders: A review
- Inherited epidermolysis bullosa: clinical and therapeutic aspects
- Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review
- Skin Development and Disease: A Molecular Perspective
- Case of non-Herlitz junctional epidermolysis bullosa with<i>COL17A1</i>mutation
- Acrodermatitis enteropathica – diagnostic challenges