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Research 451–480 of 1000+
- Exploring the Gut Microbiome and Metabolome in Individuals with Alopecia Areata Disease
- Premature graying of hairs: Ayurveda perspective
- Female doping: observations from a data lake study in the Hospital District of Helsinki and Uusimaa, Finland
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations
- A Rare Case of Keratosis Follicularis Spinulosa Decalvans Affecting a Female Child
- Moniletherix
- The malignant capacity of skin tumours induced by expression of a mutant H-ras transgene depends on the cell type targeted
- Netherton's syndrome: A syndrome of elevated IgE and characteristic skin and hair findings
- Testosterone and doping control
- Sebaceous Gland Atrophy in Psoriasis: An Explanation for Psoriatic Alopecia?
- Methotrexate for maintenance of remission in ulcerative colitis
- Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Nonscarring alopecia in systemic lupus erythematosus: A cross-sectional study with trichoscopic, histopathologic, and immunopathologic analyses
- Genetic Hair Disorders: A Review
- Profibrotic Subsets of SPP1+ Macrophages and POSTN+ Fibroblasts Contribute to Fibrotic Scarring in Acne Keloidalis
- Cow placenta extract promotes murine hair growth through enhancing the insulin - like growth factor-1
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review
- Mitochondrial-related genes as prognostic and metastatic markers in breast cancer: insights from comprehensive analysis and clinical models
- β-Catenin Signaling Evokes Hair Follicle Senescence by Accelerating the Differentiation of Hair Follicle Mesenchymal Progenitors
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome
- Dermoscopy: A rapid bedside tool to assess monilethrix
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Clinical, biochemical and mutational findings in biotinidase deficiency among Malaysian population
- What is behind the ‘swarm of bees’ in alopecia areata
- Ectodysplasin A (EDA) Signaling: From Skin Appendage to Multiple Diseases
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia