Search
for
Sort by
Research 181–210 of 1000+
- The Role of the Slc39a Family of Zinc Transporters in Zinc Homeostasis in Skin
- Protoporphyrin IX: the Good, the Bad, and the Ugly
- Actualités du SOPK
- Cytostatics and immunosuppressive drugs
- Stress and the skin: Significance of emotional factors in dermatology
- Keratinic amyloid deposition in canine hair follicle tumors
- Premature graying of hairs: Ayurveda perspective
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- HAIR AND SYSTEMATIC DISEASE
- Follikelhormone
- Phospholipase A<sub>2</sub> inhibition as potential therapy for inflammatory skin diseases
- Treatment of frontal fibrosing alopecia: literature review 2020-2025
- New food supplement cures alopecia
- Medium-dose prednisolone pulse therapy in alopecia areata
- Topical minoxidil in early male pattern baldness
- Lipid profile in androgenetic alopecia
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- Autistic-undisciplined thinking in the practice of medical trichology
- Characterization of Human Keratin-Associated Protein 1 Family Members
- Effects of AiQingHua oil on microcirculation disturbance and alopecia mice model
- Lack of the Vitamin D Receptor is Associated with Reduced Epidermal Differentiation and Hair Follicle Growth
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- Androgenetic alopecia in men
- Discovery of New Drug Therapies Based on the Study of Adverse Reactions
- The Effect of Drugs on Hair
- 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
- FLCN regulates transferrin receptor 1 transport and iron homeostasis
- Sustained clinical and psychosocial reversal of advanced male androgenetic alopecia through individualized classical homeopathy at Dr Batra’s homeopathy clinic: A longitudinal case report
- 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
- The Functional Diversity of Epidermal Keratins Revealed by the Partial Rescue of the Keratin 14 Null Phenotype by Keratin 16