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Research 661–690 of 822
- Common Skin Disorders in Pediatric Skin of Color
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Hair restoration surgery: challenges and solutions
- Genetic Hair Disorders: A Review
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- A Comprehensive Review of Mammalian Pigmentation: Paving the Way for Innovative Hair Colour-Changing Cosmetics
- Follicular Unit Extraction (FUE) Hair Transplant: Curves Ahead
- Loss of ‘Epidermal Melanin Unit’ Integrity in Human Skin During Melanoma-Genesis
- Trichoscopic Signs in Dermatomyositis, Systemic Lupus Erythematosus, and Systemic Sclerosis: A Comparative Study of 150 Patients
- Alopecia areata and subsequent Marie Antoinette syndrome following COVID-19 infection and vaccination: A case report
- The anti‐apoptotic Bcl‐2 protein regulates hair follicle stem cell function
- Diphencyprone Induced Vitiligo: A Case Report
- Exploring the dermatological applications of human mesenchymal stem cell secretome: a comprehensive review
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Trichotillomania: What Do We Know So Far?
- Making the head: Caspases in life and death
- Evaluation of cardiovascular disease risk factors in patients with mycosis fungoides
- Expert recommendations on supportive skin care for non‐surgical and surgical procedures
- Hair Graying Regulators Beyond Hair Follicle
- Clinical recognition and management of alopecia in women of color,
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- Assessment, reliability, and validity of trichoscopy in the evaluation of alopecia in women
- Keloid scars arising after follicular unit extraction hair transplantation
- A Novel Atypical Presentation of Frontal Fibrosing Alopecia Involving the Frontoparietal Scalp
- Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families
- Research Techniques Made Simple: Zebrafish Models for Human Dermatologic Disease
- Hair microscopy: an easy adjunct to diagnosis of systemic diseases in children
- Trichoscopic Findings in Androgenetic Alopecia
- Nutritional Dermatoses in the Hospitalized Patient