Search
for
Sort by
Research 781–810 of 1000+
- Risk factors and lipid metabolism characteristics of early‐onset male androgenetic alopecia: A pilot study
- Topical retinoids: role and place in acne therapy
- 874 Elevated expression of osteopontin splice variants in nonmelanoma skin cancer compared to normal skin and adult keratinocytes
- Influência de micronutrientes na queda de cabelo
- Regulation of Involucrin Gene Expression
- Evaluation of several immune and inflammatory indicators and their association with alopecia areata
- Biomarkers in alopecia Areata: A systematic review and meta-analysis.
- Cardiometabolic Risk Factors in Atorvastatin-Treated Women with Euthyroid Autoimmune Thyroiditis
- Bone Metabolism in Patients with Hidradenitis Suppurativa: A Case-control Study
- The Repair Effect of Lactobacillus Plantarum L30 on Hair Follicles in Alopecia
- Vitamin Deficiency, Dependency, and Toxicity
- Effect of antioxidant supplementation on digestive enzymes in radiation induced intestinal damage in rats
- Hereditary 1,25‐Dihydroxyvitamin D–Resistant Rickets Due to an Opal Mutation Causing Premature Termination of the Vitamin D Receptor
- Clinical and genetic findings in a Chinese family with VDR-associated hereditary vitamin D-resistant rickets
- Pharmaceutical care in the use of vitamin-mineral complexes for women during pregnancy and lactation
- Vitamin D Receptor Gene Polymorphism In Chronic Telogen Effluvium; A Case-Control Study
- An Investigation into the Effects of Water- and Fat-Soluble Vitamins in Alzheimer's and Parkinson's Diseases
- Basic Nutrition for Sports Participation, Part 2: Vitamins and Minerals
- Editorial Board
- Editorial Board
- Coda
- Protection against cyclophosphamide‐induced alopecia and inhibition of mammary tumor growth by topical 1,25‐dihydroxyvitamin D3 in mice
- Review on Herbal Hair Serum
- A Girl with a Novel Splice Site Mutation in <i>VDR</i> Supports the Role of a Ligand-Independent VDR Function on Hair Cycling
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets (HVDRR): clinical heterogeneity and long-term efficacious management of eight patients from four unrelated Arab families with a loss of function <i>VDR</i> mutation
- In This Issue
- Skinspan: A Holistic Roadmap for Extending Skin Longevity With Evidence‐Based Interventions
- Collagen Involvement in Health, Disease, and Medicine
- Spherical Skin Model: Stratified Co‐Culture of Fibroblasts and Keratinocytes on Spherical Beads Toward Compound Screening
- Hutchinson-Gilford progeria syndrome - A brief introduction