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Research 121–150 of 1000+
- A Standardized In Vitro Framework for Evaluating Hair Care Products: Hair Parameters and Efficacy Performance
- Immunological control of skin development: from homeostasis to developmental pathologies
- Atrichia congenita with papular lesions: A rare cause of pediatric alopecia
- Complete defect in PA-PLA1α secretion function leading to autosomal recessive woolly hair and hypotrichosis: insights from a novel compound heterozygous LIPH variant study in a Chinese pedigree
- Vitamin D: A Bridging Element for Wellness; A Case Study on Vitamin D Deficiency and its Association with Alopecia Areata and Other Conditions
- COVID-19 Infection and Vaccination Effects on Breast Implant Illness: A Case Report
- Effects of taxifolin from enzymatic hydrolysis of Rhododendron mucrotulatum on hair growth promotion
- Swastyayanam of Bhela indriya Sthana - an explorative study
- Aesthetics in Geriatrics Using Plasma and Its Fractions in India
- Skin Disorders in Athletes: Professional and Recreational Sports
- S235: Management of the Anterior Neck in Facial Rejuvenation
- S236: Mandibular Trauma: From the Simple to the Complex and Everything in Between
- Poster session
- Complications in Esthetic Surgery
- Secondary cicatricial and other permanent alopecias
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- A Neonate with Unexplained Hair Loss
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- Female pattern hair loss: therapeutic update
- Australasian Society for Dermatology Research Meeting, May 2006
- Giant axonal neuropathy alters the structure of keratin intermediate filaments in human hair
- Recovery of Transplanted Eyebrow From Radiation-Induced Anagen Effluvium
- Emerging 3D bioprinting applications in plastic surgery
- Severe Monilethrix Associated with Intractable Scalp Pruritus, Posterior Subcapsular Cataract, Brachiocephaly, and Distinct Facial Features: A New Variant of Monilethrix Syndrome?
- Case report: Two individuals with AEBP1-related classical-like EDS: Further clinical characterisation and description of novel AEBP1 variants
- A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene
- A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report
- AAPS and PSRC 2016 Abstract Supplement
- Expert consensus recommendations on appropriate serological testing for the chief complaint of alopecia
- Mutations in the vitamin D receptor gene in four patients with hereditary 1,25-dihydroxyvitamin D-resistant rickets