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Research 511–540 of 1000+
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- Genetically modified laboratory mice with sebaceous glands abnormalities
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Congenital Adrenal Hyperplasia
- A Comprehensive Review of Management of Patients with Infertility having Polycystic Ovarian Syndrome
- LPA-producing enzyme PA-PLA<sub>1</sub>α regulates hair follicle development by modulating EGFR signalling
- The Biology and Genomics of Human Hair Follicles: A Focus on Androgenetic Alopecia
- Trichoscopy in genetic hair shaft abnormalities
- T-Cell Reconstitution after Thymus Xenotransplantation Induces Hair Depigmentation and Loss
- Treatment of hereditary hypotrichosis simplex of the scalp with oral minoxidil and growth factors
- The Hirsute Woman: Challenges in Evaluation and Management
- Postmenopausal hyperandrogenism
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review
- The Impact of Botulinum Toxin on Hair Transplantation Outcomes: A Split-scalp Randomized Controlled Trial
- The Impact of Botulinum Toxin on Hair Transplantation Outcomes: A Split-scalp Randomized Controlled Trial
- Trichoscopy and Trichogram
- Preoperative Botulinum Toxin Injection Does Not Improve Hair Transplantation Outcomes: A Split-scalp Randomized Controlled Trial
- The Impact of Botulinum Toxin on Hair Transplantation Outcomes: A Split-scalp Randomized Controlled Trial
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Evaluating 5 alpha reductase inhibitors for the treatment of male androgenic alopecia
- A novel missense mutation (C622G) in the zinc‐finger domain of the human hairless gene associated with congenital atrichia with papular lesions
- SAT-293 Novel Presentation Of A Heterozygous INSR Mutation And Markedly Elevated Testosterone Levels In A Pediatric Patient, A Case Report.
- When the algorithm fails and experience wins: An extraordinary trichoscopic case
- Canine Follicle Stem Cell Candidates Reside in the Bulge and Share Characteristic Features with Human Bulge Cells
- Oral Presentations
- Alopecia areata: Clinical presentation, diagnosis, and unusual cases
- Novel insights into the pathways regulating the canine hair cycle and their deregulation in alopecia X
- Systematic review of mesotherapy: a novel avenue for the treatment of hair loss
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome