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Research 391–420 of 1000+
- Ectodermal Dysplasia: Variable Expressions
- When Rare Meets Risky: Clouston Syndrome with Cutaneous Squamous Cell Carcinoma
- Familial Frontal Fibrosing Alopecia Occurs Early in Daughters With Affected Mothers: A Case Report and a Review of the Literature
- Type 1 interferon signature and cytotoxic T lymphocyte activation targeted against sweat ducts in inflammatory acquired idiopathic generalized anhidrosis
- Control of lice infestation in horses using a 10 mg/mL deltamethrin topical application
- Cardiovascular Safety Signals of Oral Versus Topical Minoxidil in FAERS: A Disproportionality Analysis (Analytic Cohort 2012–2025)
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- A Comprehensive Review of Acne Vulgaris
- Comparison of Effects on Gene Expression Activity of Low-Molecular-Weight Lychee Fruit Polyphenol (Oligonol®), Adenosine, and Minoxidil in Human Dermal Papilla Cells
- Clinical overview of tinea infection in Ramadi, Iraq
- Multiple Concurrent Pilonidal Sinuses: Case report and Literature review
- Proxalutamide Reduces the Rate of Hospitalization for COVID-19 Male Outpatients: A Randomized Double-Blinded Placebo-Controlled Trial
- Update on hidradenitis suppurativa: connecting the tracts
- Androgenetic Alopecia: Clinical Treatment
- Sweat Hypersensitivity‐Induced Urticaria and Sebaceous Adenitis in an American Saddlebred
- A Systematic Scoping Review and Conceptual Analysis of New-Onset Fibromyalgia Manifestations After Non-Hospitalized COVID-19: Empirics, Definitions, Methodologies, Pathophysiology, Mapping of Literature, and Knowledge Gaps
- The Impact of Chemotherapy on the Nutritional Status of Breast Cancer Patients
- Granular Parakeratosis of the Eccrine Ostium: A Case Report
- Empirical evidence of observer bias in randomized clinical trials: updated and expanded analysis of trials with both blinded and non-blinded outcome assessors
- Frontal fibrosing alopecia: An update on the hypothesis of pathogenesis and treatment
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- E-Poster
- Therapeutic Use of Botulinum Neurotoxins in Dermatology: Systematic Review
- Questionnaire Modifications and Alternative Scoring Methods of the Dermatology Life Quality Index: A Systematic Review
- Skin manifestations associated with systemic diseases – Part I
- The protease corin regulates electrolyte homeostasis in eccrine sweat glands
- Ontogeny of Skin Stem Cells and Molecular Underpinnings
- Expert recommendations on supportive skin care for non‐surgical and surgical procedures
- Epidermal/Dermal Separation Techniques and Analysis of Cell Populations in Human Skin Sheets