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Research 241–270 of 1000+
- Lipid nanocarriers as innovative strategies for hair regrowth
- Subject Index
- Trichodystrophies: A hair-raising differential diagnosis
- Cutaneous changes in patients with chronic renal failure on hemodialysis
- Darier Sign: A Historical Note
- Diseases that Affect the Pinna
- Woodhouse-Sakati Syndrome with Unique Unreported Previous Findings
- Disorders of the skin appendages
- Molecular pathology of skin adnexal tumours
- The Significance of Scalp Involvement in Pemphigus: A Literature Review
- The urine as a diagnostic key for a homozygous EGFR mutation
- Spink5-deficient mice mimic Netherton syndrome through degradation of desmoglein 1 by epidermal protease hyperactivity
- Effects of natural products on skin inflammation caused by abnormal hormones secreted by the adrenal gland
- Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report
- Steatocystoma Multiplex
- TONGUE, RED
- Novel insights into the pathways regulating the canine hair cycle and their deregulation in alopecia X
- Focal palmoplantar callosities in non-Herlitz junctional epidermolysis bullosa
- Epidermal patterning and induction of different hair types during mouse embryonic development
- The Historical Studies Underpinning the Concept of Hair Follicle Neogenesis
- Drug Repurposing for Rare Diseases
- Treatment of pediatric alopecia areata: A systematic review
- Madarosis: A marker of many Maladies
- Cosmetic adverse effects of antiseizure medications; A systematic review
- Exploring Pediatric Dermatology in Skin of Color: Focus on Dermoscopy
- Skin Sceneries of Thyroid Disorders and Impact of Thyroid on Different Skin Diseases: A Scoping Review Focused on Pediatric Patients
- Genomic prediction and genome-wide association studies of morphological traits and distraction index in Korean Sapsaree dogs
- Clinical and Genetic Aspects of Alopecia Areata: A Cutting Edge Review
- Non‐biologic immunosuppressive drugs for inflammatory and autoimmune skin diseases
- Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review