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Research 61–90 of 1000+
- The physical and physiological effects of vacuum massage on the different skin layers: a current status of the literature
- Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: a case report and review of the literature
- Hair follicle-derived mesenchymal cells support undifferentiated growth of embryonic stem cells
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Aged Skin Cells Nurture Stem Cells toward Regeneration
- 0952 Spatial transcriptomics reveal compartmentalized dysregulation of lipid metabolism in acne vulgaris
- Rare and Underappreciated Causes of Polycystic Ovarian Syndrome
- 53607 Common Contact Allergens Implicated in Frontal Fibrosing Alopecia Found in Over-the-Counter Hair Growth Serums and Solutions
- Polycystic Ovary Syndrome and NC-CAH: Distinct Characteristics and Common Findings. A Systematic Review
- Diagnostic Challenges and Treatment Strategies in Neutrophilic Cicatricial Alopecias: A Narrative Review from Conventional Therapies to New Therapeutic Targets
- Prevalence and Metabolic Characterization of Polycystic Ovary Syndrome in a Cohort of Patients Diagnosed with Spina Bifida: Study Protocol
- Androgens and Hirsutism in a Large Cohort of Portuguese Women
- Comedonal and Cystic Fibrofolliculomas in Birt-Hogg-Dube Syndrome
- Polycystic Ovary Syndrome
- Thyroid hormone action on skin.
- Oligomenorrhoea in Exercising Women
- Free androgen index (FAI)’s relations with oxidative stress and insulin resistance in polycystic ovary syndrome
- 075 Clinical investigation of JAK inhibitor Tofacitinib in scarring alopecias
- TREATMENT OF KERATOSIS PILARIS: A NARRATIVE LITERATURE REVIEW OF TOPICAL, PROCEDURAL, AND VARIANT-SPECIFIC THERAPIES
- Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot
- New Insights into Testosterone Biosynthesis: Novel Observations from HSD17B3 Deficient Mice
- A Comprehensive Approach in Diagnosing the Polycystic Ovary Syndrome
- Single-cell RNA-seq highlights heterogeneity in human primary Wharton’s jelly mesenchymal stem/stromal cells cultured in vitro
- Complex X chromosome rearrangement associated with multiorgan autoimmunity
- Frontal fibrosing alopecia and lichen planopilaris in HLA-identical mother and daughter
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Adverse Reactions to Biologic Medications Used in Allergy and Immunology Diseases
- Clinical Usefulness of Non-Invasive Metabolic-Associated Fatty Liver Disease Risk Assessment Methods in Patients with Full-Blown Polycystic Ovary Syndrome in Relation to the MRI Examination with the Ideal IQ Sequence