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Research 871–900 of 1000+
- Antiandrogen therapy for androgenetic alopecia
- Spontaneous cutaneous adverse drug reaction reports—An analysis of a 10‐year dataset in Singapore
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- [Dermatophytic disease: exuberant hyperkeratosis with cutaneous horns].
- Recent therapeutic developments for acne
- Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response
- The role of multiomics in revealing the mechanism of skin repair and regeneration
- Exploring Variation in Ovine KRTAP19-5 and Its Effect on Fine Wool Fibre Curvature in Chinese Tan Sheep
- [Hormonal profile in men with premature androgenic alopecia].
- Identification and Characterization of Two Se6OMTs from Stephania epigaea Offer Novel Insights into the Biosynthetic Pathway of Cepharanthine
- Alopecia areata in atopic dermatitis: coincidence or regularity?
- Multiple basal cell carcinomas in a patient with myotonic dystrophy type 1
- Acquired 11β-hydroxylase Deficiency by Inhaled Etomidate and its Analogues: A Mimic of Congenital Adrenal Hyperplasia
- Exploring the clinical implications of novel SRD5A2 variants in 46,XY disorders of sex development
- Role of Csdc2 in Regulating Secondary Hair Follicle Growth in Cashmere Goats
- Exome analysis for Cronkhite-Canada syndrome: A case report
- Current and future pharmacotherapy for alopecia areata
- Polyzystisches Ovar-Syndrom (PCOS)
- Challenges associated with the identification of germline variants on myeloid malignancy genomic profiling—a Singaporean experience
- Alopesi Areata ile Depresyon İlişkisi
- Natural Skin Whitening Compounds: Types, Source and Mechanism of Action: A Review
- A Case to Tear One's Hair Out: Trichotillomania in Wilson's Disease
- Novel Androgen Receptor Gene Variant Containing a Premature Termination Codon in a Patient with Androgen Insensitivity Syndrome
- Human Hair as a Testing Substrate in the Era of Precision Medicine: Potential Role of ‘Omics-Based Approaches
- Co-occurrence of monilethrix and Type 1 diabetes mellitus
- Diagnosis and management of hair loss in children
- Highlights of Hair India 2012
- Pharmacogenomic variation and chemotherapy-related toxicity profiles in pediatric patients with cancer in Tanzania: a cross-sectional study
- Comparative Skin Transcriptomics Reveals Key Regulators of Cashmere Fiber Production in Inner Mongolian Goats