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Research 31–60 of 1000+
- Hair loss.
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- Congenital Hair Anomaly in Association with Hypodontia of Permanent Teeth: A Quiz
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Keratin disorders: from gene to therapy
- Hair Shaft Disorders
- Congenital and Hereditary Skin Diseases
- A rare cause of irrevocable childhood alopecia feigning alopecia universalis: Atrichia congenita with papular lesions
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- A case of congenital pili multigemini
- Clinical and molecular genetic studies in hereditary hair loss
- Keratins of the Human Hair Follicle
- Pachyonychia congenita: Sporadic onset with mutation analysis
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Molecular and functional aspects of the hairless (<i>hr</i>) gene in laboratory rodents and humans
- The Efficacy of Topical Minoxidil for Non-Scarring Alopecia: A Systematic Review
- Hairless is a nuclear receptor corepressor essential for skin function
- Alternative uses of dermoscopy in daily clinical practice: An update
- Cómo hacer que dos más dos sumen cinco
- Cantú Syndrome Is Caused by Mutations in ABCC9
- The eye and the skin in endocrine metabolic diseases
- Hairless: A nuclear receptor corepressor essential for skin function
- Ptosis in childhood
- FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
- Alopecia in children
- Differential diagnosis of alopetia in children and adolescents
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Hirsutism and Hypertrichosis
- Adverse Reactions to Oral Retinoids An Update
- Acne as a chronic systemic disease