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Research 751–780 of 1000+
- Defining the Cellular Environment in the Organ of Corti following Extensive Hair Cell Loss: A Basis for Future Sensory Cell Replacement in the Cochlea
- Peripheral Arterial Disease: Diagnosis and Management
- Difficult and rare forms of acne
- Mucin‐poor follicular mycosis fungoides
- Heterogeneity in the genetic alterations and in the clinical presentation of acrodermatitis enteropathic: Case report and review of the literature
- Novel Mutation in the Hemojuvelin Gene (HJV) in a Patient with Juvenile Hemochromatosis Presenting with Insulin-dependent Diabetes Mellitus, Secondary Hypothyroidism and Hypogonadism
- Porokeratotic Eccrine Ostial and Dermal Duct Nevus: A Report of Rare Late-Onset Solitary Lesion
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Primary cutaneous diffuse large B‑cell lymphoma of the scalp: A case report and brief review of the literature
- Pyoderma gangrenosum presented as generalized pustules in a patient with Crohn’s disease
- #1697882 "A" Vitamin to Consider: Refractory Hypercalcemia from Vitamin A Toxicity
- Twins with psychiatric features and a nonsense HRAS variant affecting transcript processing
- Conventional histopathology and new technologies in cutaneous mucinoses: Old diagnostic criteria and new therapeutic perspectives
- Structural and Immunocytochemical Characterization of Keratinization in Vertebrate Epidermis and Epidermal Derivatives
- Cylindroma as Tumor of Hair Follicle Origin
- Giant axonal neuropathy alters the structure of keratin intermediate filaments in human hair
- Porcine acellular dermal matrix facilitates hair follicle stem cells entering the hair cycle in C57/BL6 mice
- 470 Exploring the possible involvement of skin-resident memory T cells in refractory chronic alopecia areata
- The Role of PPARβ/δ-Related Lipid Metabolism in High-Altitude Adaptation of Yak Coat Based on Proteomics and Metabolomics
- Patients with Compound Heterozygous Mutations in Forkhead Box N1 have a Severe Immunodeficiency while Maintaining Normal Skin and Hair Development
- Studies on basal cell carcinoma with emphasis on the role of the human homologue of the Drosophila patched gene
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Nutritional and Microbial Strategies for Treating Acne, Alopecia, and Atopic Dermatitis
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome
- Synaptic‐like vesicles and candidate transduction channels in mechanosensory terminals
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Abstracts
- Green and Emerging Microextraction Strategies for Bioanalytical Determination of Hormones: Trends, Challenges, and Applications
- Male androgenetic alopecia
- Acrodermatitis Enteropathica: A Case Report Involving a Delayed Diagnosis