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Research 391–420 of 1000+
- Delphi Consensus on Attenuated Androgen Use for Long‐Term Prophylaxis in Hereditary Angioedema: AURA Project
- Male androgenetic alopecia
- Resistance to the Insulin and Elevated Level of Androgen: A Major Cause of Polycystic Ovary Syndrome
- The Effects of Lower vs Higher Cell Number of Platelet-Rich Plasma (PRP) on Hair Density and Diameter in Androgenetic Alopecia (AGA): A Randomized, Double-Blinded, Placebo, Parallel-Group Half-Scalp IRB-Approved Study.
- Study of the international epidemiology of androgenetic alopecia in young caucasian men using photographs from the internet
- A Multimodal Hair-Loss Treatment Strategy Using a New Topical Phytoactive Formulation: A Report of Five Cases
- Trichilemmal cyst of the neck: case report and review of the literature
- H3K9me3 controls epidermis morphogenesis by regulating RNA Pol II dynamics at developmental promoters and enhancers
- Bioactive Compound-Loaded Nanocarriers for Hair Growth Promotion: Current Status and Future Perspectives
- Proceedings of the Ninth World Congress for Hair Research (2015)
- Minoxidil to Treat Androgenetic Alopecia in Men and Women: What is It & How does It Work?
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Current Advanced Therapies Based on Human Mesenchymal Stem Cells for Skin Diseases
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- ABCD1 Gene Mutations: Mechanisms and Management of Adrenomyeloneuropathy
- Hair shaft disorders in children – An update
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- Understanding sex and gender disparities in COVID-19 mortality: a narrative review beyond biology
- Zebrafish Model of Hereditary Pigmentary Disorders
- Effects of Androgen Treatment on Growth in Patients with 5-α-Reductase Type 2 Deficiency
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Regulation of stem cell function by protein ubiquitylation
- Defolliculated (Dfl): A Dominant Mouse Mutation Leading to Poor Sebaceous Gland Differentiation and Total Elimination of Pelage Follicles
- Ichthyosis with confetti: clinics, molecular genetics and management
- The Genetic Architecture of Alopecia Areata
- Transglutaminase 3: The Involvement in Epithelial Differentiation and Cancer
- Atrichia with papular lesions in two Pakistani consanguineous families resulting from mutations in the human hairless gene
- Sex Identification of Feather Color in Geese and the Expression of Melanin in Embryonic Dorsal Skin Feather Follicles