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Research 721–750 of 1000+
- Bazi Bushen capsule alleviates skin photoaging by targeting the KEAP1–NRF2 pathway
- Platelet-Rich Concentrates in the Management of Lichen Planus—A Comprehensive Review
- Effectiveness and tolerance of medicated shampoo containing selenium sulfide and salicylic acid in patients with seborrheic dermatitis
- A scientometric study on research trends and characteristics of discoid lupus erythematosus
- A Retrospective Evaluation of the Laboratory Findings of Dermatology Patients Whose Biotin Levels Were Checked
- Alopecia in Patients with Collagen VI-Related Myopathies: A Novel/Unrecognized Scalp Phenotype
- Trichoscopy as an essential diagnostic technique for hair and scalp disorders in skin of color: A case-control study
- Cronkhite-Canada Syndrome: A Case Report and Literature Review of Gastrointestinal Polyposis Syndrome
- Dermatologic Manifestations of Mitochondrial Dysfunction: A Review of the Literature
- Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness
- Hair follicles modulate skin barrier function
- Eyebrow and Eyelash Alopecia: A Clinical Review
- Trichoscopic Findings in Androgenetic Alopecia
- Trichoscopy pattern in alopecia areata: A systematic review and meta‐analysis
- Utility of trichoscopy
- Recent Advances in Understanding of the Etiopathogenesis, Diagnosis, and Management of Hair Loss Diseases
- Validity and Advantages of Three-Dimensional High-Frequency Ultrasound in Dermatological Evaluation
- Clinical and Trichoscopic Graded Live Visual Scale for Androgenetic Alopecia
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- A Novel Epithelial Keratin, hK6irs1, is Expressed Differentially in All Layers of the Inner Root Sheath, Including Specialized Huxley Cells (Flügelzellen) of the Human Hair Follicle
- Cellular senescence in skin‐related research: Targeted signaling pathways and naturally occurring therapeutic agents
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Genetic Hair Disorders: A Review
- Poster Presentations
- Topical Treatment for Scarring and Non-Scarring Alopecia: An Overview of the Current Evidence
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Mechanisms of autophagy and their implications in dermatological disorders
- Clinical recognition and management of alopecia in women of color,
- A Three-Step Diagnostic Algorithm for Alopecia: Pattern Analysis in Trichoscopy
- Lichen Planopilaris Responsive to a Novel Phytoactive Botanical Treatment: A Case Series