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Research 61–90 of 77
- Chronic overlapping pain conditions and nociplastic pain
- Lifestyle Factors Involved in the Pathogenesis of Alopecia Areata
- The atypical ‘hippocampal’ glutamate receptor coupled to phospholipase D that controls stretch‐sensitivity in primary mechanosensory nerve endings is homomeric purely metabotropic GluK2
- Calcium in Root Hair Growth
- Cellular Senescence and Aging in Myotonic Dystrophy
- Wound Healing Effects of New Cream Formulations with Herbal Ingredients
- Effects of natural products on skin inflammation caused by abnormal hormones secreted by the adrenal gland
- Faces of the Face
- Calcium in Root Hair Growth
- A pilot study to explore postpartum body image and resumed menstruation
- Black hair dye dermatitis: Still a major skin problem and commonly mimicking chronic actinic dermatitis
- Programmed nanozyme hydrogel enabling spatiotemporal modulation of wound healing achieves skin regeneration after biofilm infection
- Beyond the usual: a case of acrodermatitis enteropathica clinically resembling erythrokeratoderma variabilis
- Saponins of Paris polyphylla for the Improvement of Acne: Anti-Inflammatory, Antibacterial, Antioxidant and Immunomodulatory Effects
- Precision Dermatology: A Review of Molecular Biomarkers and Personalized Therapies
- An overview of animal models induced by glucocorticoids
- Systemic Antifungals
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- The fundamentals of WNT10A
- Inherited Disorders of the Hair
- Trichoscopy in Hair Shaft Disorders
- <i>WNT10A</i> , dermatology and dentistry
- Hypotrichosis in a child with olmsted syndrome
- Molecular pathology of skin adnexal tumours
- Diseases of Periocular Hair
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Decades of progressive red and yellow nodules
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders