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Research 751–780 of 1000+
- Evaluation of vitamin D in pediatric alopecia areata: A case–control study of thirty patients in a tertiary care hospital
- JAK-Inhibitors Beyond the Label: Emerging Applications in Dermatology
- Ophthalmologic Comorbidities in Alopecia Areata
- Real-world evidence in alopecia areata treatment: A narrative review
- Hair Transplantation in Primary Cicatricial Alopecias: A Review and Update
- Zinc transporter ZIP13 G289R variant from Spondylocheirodysplastic Ehlers-Danlos syndrome (SCD-EDS) is associated with abnormal hair quality
- AUTOIMMUNE CICATRICIAL ALOPECIA AND THE ROLE OF TRICHOSCOPY IN ITS DIAGNOSIS: A LITERATURE REVIEW
- Treatment of Lichen Planopilaris and Frontal Fibrosing Alopecia: A Retrospective, Real-Life Analysis in a Tertiary Center in Germany
- Insights into Alopecia Areata: A Systematic Review of Prevalence, Pathogenesis, and Psychological Consequences
- The role of fractional laser‐assisted drug delivery in enhancing the efficacy of topical bimatoprost solution in the treatment of alopecia areata: An intra‐patient comparative randomized clinical trial
- A Prospective Study of Dermoscopic and Ultrastructural Features of Vitiligo-Associated Leukotrichia
- Multi-omics analysis of functional substances and expression verification in cashmere fineness
- Establishing the financial burden of alopecia areata and its predictors
- Alopecias: Practical Tips for the Management of Biopsies and Main Diagnostic Clues for General Pathologists and Dermatopathologists
- Novel association of trichothiodystrophy with autoimmune thyroiditis and autoimmune hemolytic anemia: A case report
- Alopecia areata: a review of diagnosis, pathogenesis and the therapeutic landscape
- Frontal fibrosing alopecia
- Overview of Alopecia Areata
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- Characteristics of Androgenetic Alopecia in Asian
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Conversion of the Nipple to Hair-Bearing Epithelia by Lowering Bone Morphogenetic Protein Pathway Activity at the Dermal-Epidermal Interface
- Ichthyosis with confetti: clinics, molecular genetics and management
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Syphilitic alopecia: uncommon trichoscopic findings
- Inherited epidermolysis bullosa: clinical and therapeutic aspects
- Novel Mutations in X-Linked Dominant Chondrodysplasia Punctata (CDPX2)
- μ-Crystallin, Thyroid Hormone-binding Protein, is Expressed Abundantly in the Murine Inner Root Sheath Cells
- Regenerative Medicine-Based Treatment for Vitiligo: An Overview