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Research 11
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- <i>WNT10A</i> , dermatology and dentistry
- Insulin sensitivity, androgens and isotretinoin therapy in women with severe acne
- Insulin resistance is increased in alopecia areata patients
- The use of complementary and alternative medicine among dermatology outpatients in Eastern Turkey
- The mechanism of activated platelet‐rich plasma supernatant promotion of hair growth by cultured dermal papilla cells
- Elastic Staining in Differentiating Between Follicular Streamers and Follicular Scars in Horizontal Scalp Biopsy Sections
- Inherited Disorders of the Hair
- Phototherapy in Childhood
- Selenium Compounds and Their Bioactivities: Molecular Mechanisms and Prospects for Functional Food and Therapeutic Applications