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Research 121–150 of 1000+
- Benefit-Risk Assessment of GLP-1 Receptor Agonists: Implications for Dermatologists and Plastic Surgeons
- A study on common clinical pattern of presentation of skin and hair changes in nutritional deficiencies associated with dietary fallacies in children 1 to 5 years of age
- The Skin and Subcutaneous Tissues
- Multiple Benign Epidermal Inclusion Cysts Clinically Misdiagnosed as Rhinophyma: A Case Report
- Description of skin lesions
- Mucocutaneous Manifestations of Endocrine Disorders
- Stem cells and aberrant signaling of molecular systems in skin aging
- Diseases that Affect the Pinna
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Kaposi varicelliform eruption
- Epidermal mammalian target of rapamycin complex 2 controls lipid synthesis and filaggrin processing in epidermal barrier formation
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- An Infant with Worsening Rash
- TONGUE, RED
- Disorders of Keratinization
- Investigating the role of keratin proteins and microbial associations in hereditary and pathogenic alopecia
- Molecular Genetics of Human Hair Diseases
- Ankyloblepharon-ectodermal dysplasia-clefting syndrome: Surgical and medical management in an infant with bilateral corneal perforations
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Focal palmoplantar callosities in non-Herlitz junctional epidermolysis bullosa
- Effects of natural products on skin inflammation caused by abnormal hormones secreted by the adrenal gland
- Mesenchymal Stem Cells for the Treatment of Skin Diseases
- Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review
- The molecular basis of human keratin disorders
- Desmoglein 4 is regulated by transcription factors implicated in hair shaft differentiation
- Current Genetics in Hair Diseases
- Genetic Hair Disorders: A Review
- A Three-Step Diagnostic Algorithm for Alopecia: Pattern Analysis in Trichoscopy