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Research 451–480 of 1000+
- Molecular Genetics of Alopecias
- Women's Skin throughout Lifetime
- Follicular Map: A Novel Approach to Quantitative Trichoscopy
- Practice and Educational Gaps in Dermatology
- Vibration assisted analgesia during intralesional corticosteroid therapy for alopecia
- Curl pattern classification: A potential tool for communication and risk stratification
- Regenerative Treatments: Microneedling and PRP
- Diagnostic and grading criteria for androgenetic alopecia using dermoscopy
- What is Alopecia?
- BaldGraphFormer: An Explainable Deep Learning Framework for Early Baldness Prediction by Integrating Swin Transformer, Graph Attention Networks and Clinical Features
- In silico analysis of imprinted gene expression in the mouse skin
- Histopathology of non-scarring alopecia
- Generation of folliculogenic human epithelial stem cells from induced pluripotent stem cells
- Alopecia in Children: The Most Common Causes
- Diagnosis: Alopecia areata or not?
- TRP Channels in Skin Biology and Pathophysiology
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- Histopathologic Evaluation of Alopecias
- Learning from nudity: lessons from the nude phenotype
- Inhibition of skin 5α-reductase by oral contraceptive progestins<i>in vitro</i>
- Central scalp alopecia photographic scale in AfricanAmerican women
- The utility of elastic Verhoeff-Van Gieson staining in dermatopathology
- FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
- Unveiling the Roots of Monogenic Genodermatoses: Genotrichoses as a Paradigm
- Pharmacokinetic parameters and mechanisms of inhibition of rat type 1 and 2 steroid 5α-reductases: determinants for different in vivo activities of GI198745 and finasteride in the rat 3 3Abbreviations: r5AR1, rat 5α-reductase 1; r5AR2, rat 5α-reductase 2; and DHT, dihydrotestosterone.
- Pigmented Casts
- Tissue-Selective Regulation of Androgen-Responsive Genes
- Histologic Features of Alopecias–Part I: Nonscarring Alopecias
- Tricoses compulsivas
- Dermatological aspects of the S2k guidelines on Down syndrome in childhood and adolescence