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Research 121–150 of 1000+
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Expansion of the spectrum of ITGB6-related disorders to adolescent alopecia, dentogingival abnormalities and intellectual disability
- Characterization of X‐linked hypohidrotic ectodermal dysplasia (XL‐HED) hair and sweat gland phenotypes using phototrichogram analysis and live confocal imaging
- Identifying novel strategies for treating human hair loss disorders: Cyclosporine A suppresses the Wnt inhibitor, SFRP1, in the dermal papilla of human scalp hair follicles
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- Healing hair naturally: A focus on herbal treatment for hair disorders
- 1435 Dynamic morphogen-p63 chromatin interactions that guide epigenetic changes and p63 activity in surface ectoderm commitment
- Clinical Case Notes. Lipoid proteinosis: a rare disorder with pathognomonic lid lesions
- Steroid 5α-Reductase as a Novel Therapeutic Target for Schizophrenia and Other Neuropsychiatric Disorders
- Breakdown of Immune Tolerance in AIRE-Deficient Rats Induces a Severe Autoimmune Polyendocrinopathy–Candidiasis–Ectodermal Dystrophy–like Autoimmune Disease
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- A mutation in the hair matrix and cuticle keratin KRTHB5 gene causes ectodermal dysplasia of hair and nail type
- Dermatopathology and molecular genetics
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Ankyloblepharon-ectodermal dysplasia-clefting syndrome: Surgical and medical management in an infant with bilateral corneal perforations
- The Autoimmune Regulator (AIRE), Which Is Defective in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy Patients, Is Expressed in Human Epidermal and Follicular Keratinocytes and Associates With the Intermediate Filament Protein Cytokeratin 17
- Hair Shaft Disorders
- Alopecia areata in a patient with WNT10A heterozygous ectodermal dysplasia
- Molecular Dissection of Mesenchymal–Epithelial Interactions in the Hair Follicle
- Diagnosis and Management of Alopecia in Children
- Hair loss in children.
- Nutritional Disorders of the Hair and Their Management
- Stem Cell Use to Treat Dermatological Disorders
- Third World Congress of the International Academy of Cosmetic Dermatology
- FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
- Hair Loss in Children
- Hypohidrotic Ectodermal Dysplasia with c.28delG Mutation in Ectodysplasin A Gene and Severe Atopic Dermatitis Treated Successfully with Tofacitinib
- Plakophilin 1 suppresses keratinocyte innate immune responses through DExD/H helicases
- Control of pelage hair follicle development and cycling by complex interactions between follistatin and activin