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Research 571–600 of 1000+
- Infertility: Evaluation and Initial Management
- Hereditary Hypotrichosis and Localized Morphea: A New Clinical Entity
- An animal study on the effectiveness of platelet-rich plasma as a direct pulp capping agent
- Cronkhite-Canada Syndrome: A Case Report
- Ectodysplasin-A2 induces dickkopf 1 expression in human balding dermal papilla cells overexpressing the ectodysplasin A2 receptor
- Identification of differentially expressed genes in actinic keratosis samples treated with ingenol mebutate gel
- A Case Report of Werner’s Syndrome With a Novel Mutation From India
- Clinical experience on follicular unit extraction megasession for severe androgenetic alopecia
- 1310 Anti-aging effects of retinoid hydroxypinacolone retinoate on skin models
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Glycolytic Dysfunction in Granulosa Cells and Its Contribution to Metabolic Dysfunction in Polycystic Ovary Syndrome
- Development of squamous cell carcinoma from erythroplasia of Queyrat following photodynamic therapy
- Hypothyroidism in Dogs
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- THE PEDIATRICIAN AND THE SEXUALLY ACTIVE ADOLESCENT
- The urine as a diagnostic key for a homozygous EGFR mutation
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Telogen effluvium: a review
- Biotin
- Inconsolable Crying in Infants: Differential Diagnosis in the Pediatric Emergency Department
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Spatial variation and associated genes of total hair follicle density in goats
- Diagnosis and treatment of polycystic ovarian syndrome: an update
- Hereditary vitamin D resistant rickets (HVDRR) case series: phenotype, genotype, conventional treatment, and adjunctive cinacalcet therapy
- Progeria (Hutchinson-Gilford Syndrome): Literature Review and Clinical Case
- Characterization of Primary Cilia and Intraflagellar Transport 20 in the Epidermis
- 1313 Fzd2 controls multiple aspects of epidermal development through distinct signaling mechanisms
- Diuretics
- Diagnosis and management of hair loss in children
- Trichodystrophies: A hair-raising differential diagnosis