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Research 271–300 of 1000+
- Cantú Syndrome Is Caused by Mutations in ABCC9
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Ptosis in childhood
- A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene
- Single and repeated dose of finasteride topical solution in subjects with androgenetic alopecia: A pharmacokinetic and pharmacodynamic study
- Global and exponential stabilization of a chemotactic alopecia areata model with signal-dependent diffusion and sensitivity
- Dacomitinib-Induced Paronychia Associated With PRIDE Syndrome in a Patient With Non-Small Cell Lung Cancer
- 원저 : 원형탈모증의 cyclosporine 병합치료
- Therapeutic Effect of Superficial Scalp Hypothermia on Chemotherapy-Induced Alopecia in Breast Cancer Survivors
- Long-pulsed 1064 nm Nd:YAG laser treatment for ingrown toenails and pincer nails
- Clinical Case Notes. Retinoblastoma, microphthalmia and the chromosome 13q deletion syndrome
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- PRIDE syndrome with lumbosacral hypertrichosis
- Transcriptomics analysis reveals molecular alterations underpinning spaceflight dermatology
- A cross-sectional study of clinical, dermoscopic, histopathological, and molecular patterns of scalp melanoma in patients with or without androgenetic alopecia
- Significant Correction of Disease after Postnatal Administration of Recombinant Ectodysplasin A in Canine X-Linked Ectodermal Dysplasia
- Management of congenital ichthyoses: European guidelines of care, part two
- Prevalence and associated factors of skin diseases in aged nursing home residents: a multicentre prevalence study
- Cutaneous Blood Flow.
- Subject Index
- Network-Based Drug Repositioning: Approaches, Resources, and Research Directions
- When Rare Meets Risky: Clouston Syndrome with Cutaneous Squamous Cell Carcinoma
- Case Report: 8 years old boy with neurofibromatosis type one and Alopecia from KING ABDULAZIZ MEDICAL CITY OF THE NATIONAL GUARD. Saudi Arabia
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- Hirsutism-A Comprehensive Update of Embryology, Aetiopathogenesis and Therapeutic Approach
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- An Autophagy-Related Kinase Is Essential for the Symbiotic Relationship between <i>Phaseolus vulgaris</i> and Both Rhizobia and Arbuscular Mycorrhizal Fungi
- Enhancing Permeation of Drug Molecules Across the Skin via Delivery in Nanocarriers: Novel Strategies for Effective Transdermal Applications
- Novel Mutations in X-Linked Dominant Chondrodysplasia Punctata (CDPX2)
- RoPod, a customizable toolkit for non-invasive root imaging, reveals cell type-specific dynamics of plant autophagy