Search
for
Sort by
Research 301–330 of 1000+
- Loose anagen hair syndrome: Treatment with systemic minoxidil characterised by marked hair colour change
- Hutchinson-Gilford syndrome: History, causes, phenotype and research advances
- Keratins of the Human Hair Follicle
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Comparative Anatomy of Mouse and Human Nail Units
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
- Skin Development and Disease: A Molecular Perspective
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Acne Syndromes and Mosaicism
- Systemic Comorbidities in Central Centrifugal Cicatricial Alopecia: A Systematic Review and Meta-analysis
- Madarosis: A marker of many Maladies
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Skin and hair abnormalities of Cantu syndrome: A congenital hypertrichosis due to a genetic alteration mimicking the pharmacological effect of minoxidil
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- Management OF Patients with Polycystic Ovary Syndrom
- Monilethrix Treated with Minoxidil
- Rabson-Mendenhall syndrome: two case reports and a brief review of the literature
- A rare pediatric case of loose anagen hair syndrome
- Polycystic Ovarian Syndrome: The Androgenized Adolescent
- Loose anagen hair syndrome
- Atlas of Geriatric Dermatology
- Genetic, hormonal and metabolic aspects of PCOS: an update
- A Case of Familial Male-limited Precocious Puberty with a Novel Mutation
- Keratosis pilaris atrophicans faciei: An observational, descriptive, retrospective clinical study
- Syndromes of Severe Insulin Resistance (SSIRs)
- The pharmacology of methotrexate
- Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy