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Research 841–870 of 1000+
- Ptosis in childhood
- Suppression of Vitamin D Receptor and Induction of Retinoid X Receptor α Expression During Squamous Differentiation of Cultured Keratinocytes
- The effect of dietary modulation of sulfur amino acids on cystathionine β synthase–deficient mice
- Estimating the risk of irreversible post-SSRI sexual dysfunction (PSSD) due to serotonergic antidepressants
- The Fate of Epidermal Tight Junctions in the stratum corneum: Their Involvement in the Regulation of Desquamation and Phenotypic Expression of Certain Skin Conditions
- Integrated Lipidomics in the Secreted Phospholipase A2 Biology
- Erosive Pustular Dermatosis: A Manifestation of Immunosenescence A Report of 8 Cases
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- Clinical, biochemical and mutational findings in biotinidase deficiency among Malaysian population
- Essential Role of STAT3 Signaling in Hair Follicle Homeostasis
- Monilethrix in three generations
- Sexual function in women with androgen excess disorders: classic forms of congenital adrenal hyperplasia and polycystic ovary syndrome
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- “Structural imprinting” of the cutaneous immune effector function
- Society for Endocrinology Clinical Practice Guideline for the Evaluation of Androgen Excess in Women
- Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families
- Inflammatory loops in the epithelial–immune microenvironment of the skin and skin appendages in chronic inflammatory diseases
- Ichthyosis follicularis alopecia and photophobia syndrome:Transient improvement with oral isotretinoin
- Acquired 11β-hydroxylase Deficiency by Inhaled Etomidate and its Analogues: A Mimic of Congenital Adrenal Hyperplasia
- A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report
- Novel Compound Heterozygous Variants in the CDC6 Gene in a Russian Patient with Meier-Gorlin Syndrome
- Successful plasmapheresis and immunoglobulin treatment for severe lipid storage myopathy: Doing the right thing for the wrong reason
- Congenital atrichia associated with nevus flammeus: A rare association
- Repurposing With Purpose: Treatment of Bachmann–Bupp Syndrome With Eflornithine and Implications for Other Polyaminopathies
- Anatomy and Biology of Hair at Different Ages
- Rapid Characterization of the Functional and Pharmacological Consequences of Cantú Syndrome K<sub>ATP</sub>Channel Mutations in Intact Cells
- Morphologic Markers of Acute and Chronic Stress in Child Abuse
- ILC3s as central regulators of mucosal homeostasis and disease pathogenesis (Review)
- Single-Cell Omics Advances in Understanding Tissue Development and Complex Trait Formation in Sheep and Goats
- Immunomodulatory roles of regulatory T cells in cutaneous wound healing: mechanisms and therapeutic opportunities