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Research 151–180 of 1000+
- Molecular and functional aspects of the hairless (<i>hr</i>) gene in laboratory rodents and humans
- Woolly hair generalizado: caso clínico e revisão da literatura
- Cantú Syndrome Is Caused by Mutations in ABCC9
- Alternative uses of dermoscopy in daily clinical practice: An update
- Hairless is a nuclear receptor corepressor essential for skin function
- Hair Loss in Children
- Hair follicles and their role in skin health
- Clinical relevance of hair microscopy in alopecia
- Alopecia in children
- Novel small‐insertion mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis
- Hair Loss in Children
- Genetic Defects of Female Sexual Differentiation
- Cómo hacer que dos más dos sumen cinco
- The Efficacy of Topical Minoxidil for Non-Scarring Alopecia: A Systematic Review
- A Review on-Types and Treatment of Alopecia
- FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
- Hirsutism in Women.
- Differential diagnosis of alopetia in children and adolescents
- The hair in childhood and old age
- Keratins of the Human Hair Follicle
- Is thyrotropin-releasing hormone a novel neuroendocrine modulator of keratin expression in human skin?
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Steroidogenesis of the testis – new genes and pathways
- Polycystic Ovary Syndrome and NC-CAH: Distinct Characteristics and Common Findings. A Systematic Review
- Hirsutism in Children: A Comprehensive Review of Etiology, Clinical Evaluation and Contemporary Management
- Clinical and molecular genetic studies in hereditary hair loss
- Hairless: A nuclear receptor corepressor essential for skin function
- Congenital Hair Anomaly in Association with Hypodontia of Permanent Teeth: A Quiz
- 7745 Hirsutism in young girls, Beyond PCOS
- An Approach to the Patient With Hirsutism