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Research 961–990 of 1000+
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review
- Pediatric adrenocortical carcinoma complicated by uric acid nephrolithiasis: a unique case report
- Familial Frontal Fibrosing Alopecia Occurs Early in Daughters With Affected Mothers: A Case Report and a Review of the Literature
- Natural phenylethanoid glycoside forsythoside A alleviates androgenetic alopecia by selectively inhibiting TRPV3 channels in mice
- Sequencing KRT71 as a candidate gene for hair shape variation in dromedary camels
- Alopecia universalis with IL-12-RB1 and STAT4 mutations effectively treated with upadacitinib
- Updates to Male Infertility: AUA/ASRM Guideline (2024)
- Effects of Biomaterials Derived from Germinated Hemp Seeds on Stressed Hair Stem Cells and Immune Cells
- An induced pluripotent stem cell-based approach for hair follicle development and regeneration
- Integrated edge information and pathway topology for drug-disease associations
- Pathogenesis of Alopecia Areata and Vitiligo: Commonalities and Differences
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- Tangled Truths: Unraveling the Link Between Frontal Fibrosing Alopecia and Allergic Contact Dermatitis
- Spatiotemporal Expression and Haplotypes Identification of KRT84 Gene and Their Association with Wool Traits in Gansu Alpine Fine-Wool Sheep
- Insights into Alopecia Areata: A Systematic Review of Prevalence, Pathogenesis, and Psychological Consequences
- In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis
- Molecular Aspects of Polycystic Ovarian Syndrome in Female Population in Karnataka at the Southwestern Region of India
- Molecular Aspects of Polycystic Ovarian Syndrome in Female Population in Karnataka at the Southwestern Region of India
- A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report
- Peculiarities of clinical course and diagnostic of alopecia areata with comorbidity. Clinical observations
- Editor's evaluation: Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Insulin resistance as risk factor for the development of type 2 diabetes mellitus: a systematic approach
- Frontal Fibrosing Alopecia – a review and a practical guide for clinicians
- Utilizing functional genomics approaches to characterize risk genes in alopecia areata
- A perspective on predictive markers of alopecia
- The First Visit: Consult and Workup Before Sperm Banking
- Acne Vulgaris
- Muir-torre syndrome in two families in Leicestershire, United Kingdom
- Male Androgenetic Alopecia