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Research 31–60 of 96
- Acne
- Outcomes of Tissue Expander Application for Scalp Reconstruction in Extensive Aplasia Cutis Congenita
- Interpretation of Laboratory Data and General Physical Examination by Pharmacists
- The role of versican in the skin ECM and its interaction with hyaluronic acid
- Acne
- Acne and acneiform eruptions
- Trichodystrophies: A hair-raising differential diagnosis
- Hoxc13 polyglycine repeat gain-of-function drives mammalian integument evolution by altering targeted genes and interactions
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- When the algorithm fails and experience wins: An extraordinary trichoscopic case
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- Subject Index
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- 879 Molecular network of Smads and Id2 genes in hair follicle stem cells regulation
- 878 Influence of bovine milk oligosaccharides on sebocyte lipid content and inflammatory mediators
- 883 Hair follicle bulb developed as 3D scaffold free microtissue
- Genetic Defects of Female Sexual Differentiation
- Delayed Puberty
- Adams–Oliver syndrome: new evidence in variable expressivity?
- Topical ketoconazole: a systematic review of current dermatological applications and future developments
- Short anagen syndrome
- Monilethrix
- Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report
- Commentary 2
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- Progressive Hair Loss and Myocardial Degeneration in Rough Coat Mice: Reduced Lysyl Oxidase-Like (LOXL) in the Skin and Heart
- Monilethrix: a typical case report with microscopic and dermatoscopic findings
- Homozygous Nonsense Mutation in DSC3 Resulting in Skin Fragility and Hypotrichosis
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- Monilethrix, a rare inherited hair shaft disorder in siblings