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Research 181–210 of 1000+
- Molecular Genetics of Alopecias
- Hair loss in children.
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- LAMELLAR ICHTHYOSIS: ONE CASE REPORT
- Ultraviolet-Enhanced Trichoscopy—A New Tool to Assess Pili Annulati
- Congenital atrichia and hypotrichosis
- Oral Manifestations of Hematologic and Nutritional Diseases
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- Clomiphene Citrate versus Letrozole for Ovulation Induction in PCOS: A Comparative Study
- Skin diseases in consequence of endocrine alterations
- The natural history of androgenetic alopecia
- Hair Loss in Children
- Hairless is a nuclear receptor corepressor essential for skin function
- Obesity and the skin
- Acquired scalp alopecia. Part I: A review
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Hair Loss in Children
- Isoallopregnanolone reduces tic‐like behaviours in the D1 CT ‐7 mouse model of Tourette syndrome
- Clinical relevance of hair microscopy in alopecia
- The eye and the skin in endocrine metabolic diseases
- Trichodystrophies: A hair-raising differential diagnosis
- Frontal fibrosing alopecia and ulerythema ophryogenes as two entites that can transist one into another
- Hair follicles and their role in skin health
- Management of congenital ichthyoses: European guidelines of care, part two
- Localisation and regulation of cholesterol transporters in the human hair follicle: mapping changes across the hair cycle
- What does acne genetics teach us about disease pathogenesis?
- Beyond Expectations
- Primary cicatricial alopecias
- Familial Pure Hair–Nail Ectodermal Dysplasia in Yemen: A Father–Son Case Report with Clinical Correlation
- Immunological control of skin development: from homeostasis to developmental pathologies