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Research 121–150 of 1000+
- What does acne genetics teach us about disease pathogenesis?
- Hair Loss in Children
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II
- Male fertility and skin diseases
- Evaluation of SALT score severity in correlation with trichoscopic findings in alopecia areata: a study of 303 patients
- Diseases of Periocular Hair
- Hair loss and its management in children
- Darier Sign: A Historical Note
- Role of the Wnt signaling pathway in keratoacanthoma
- Trichodystrophies: A hair-raising differential diagnosis
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- Hair Loss in Children
- Disorders of the skin appendages
- Journal Watch
- LITERATURE REVIEW
- Mesenchymal–epithelial interactions during hair follicle morphogenesis and cycling
- The British Society for Rheumatology guideline for the management of systemic lupus erythematosus in adults
- A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features
- Alopecia Areata: A tissue specific autoimmune disease of the hair follicle
- Molecular biology of hair morphogenesis: Development and cycling
- Biology of the wool follicle: an excursion into a unique tissue interaction system waiting to be re‐discovered
- Acne-associated syndromes: models for better understanding of acne pathogenesis
- Olfactory receptor OR2AT4 regulates human hair growth
- Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen
- Congenital hair loss disorders: Rare, but not too rare
- Tissue resident and follicular Treg cell differentiation is regulated by CRAC channels
- The spectrum of hair loss in patients with mycosis fungoides and Sézary syndrome