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- Focal palmoplantar callosities in non-Herlitz junctional epidermolysis bullosa
- Semidominant Inheritance in Epidermolytic Ichthyosis
- Therapeutic Use of Botulinum Neurotoxins in Dermatology: Systematic Review
- Botulinum Toxin Off-Label Use in Dermatology: A Review
- Cutaneous Manifestations of Eating Disorders
- Cutaneous Manifestations of Eating Disorders
- Author Index
- Building Models for Keratin Disorders
- PA05 A rare case of cardiocutaneous syndrome in a young child
- 410 Oral dysbiosis in palmoplantar pustulosis patients with arthro-osteosis
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- RSPO1-mutated keratinocytes from palmoplantar keratoderma display impaired differentiation, alteration of cell–cell adhesion, EMT-like phenotype and invasiveness properties: implications for squamous cell carcinoma susceptibility in patients with 46XX disorder of sexual development
- Palmoplantar pustulosis–like eruption following tofacitinib therapy for juvenile idiopathic arthritis
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- DSP c.6310delA p.(Thr2104Glnfs*12) associates with arrhythmogenic cardiomyopathy, increased trabeculation, curly hair, and palmoplantar keratoderma
- Successful Treatment of Adalimumab-Induced Paradoxical Skin Reactions in Pustulotic Arthro-Osteitis With Guselkumab
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- When Rare Meets Risky: Clouston Syndrome with Cutaneous Squamous Cell Carcinoma
- Scalp Involvement in Primary Cutaneous Lymphomas—An Update on Clinical Presentation, Diagnostics, and Management
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations
- Papillon–Lefèvre Syndrome: A Rare Case Report of Two Brothers and Review of the Literature
- 413 DC-HIL+ myeloid-derived suppressor cells are elevated in the peripheral blood and lesional skin of cutaneous lupus patients
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- 414 A fitst-in-human study of BLZ-100 (tozuleristide) demonstrates tolerability and fluorescence contrast in skin cancer
- 412 High amphiregulin expression is a high-risk feature of acute graft-versus-host disease of the skin
- Dermatoscopy of hair shaft disorders
- Psoriatic Skin Lesions Induced by Certolizumab Pegol
- Symmetrical acrokeratoderma: A peculiar entity in China? Clinicopathologic and immunopathologic study of 34 new cases
- Cutaneous Side Effects of Chemotherapy and Radiotherapy
- Thyroid Autoimmunity in Patients with Skin Disorders