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Research 91–120 of 1000+
- Hair loss
- Perspectives on Dermatopathology
- HAIR AND SYSTEMATIC DISEASE
- Thyroid hormone action on skin
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Expression Profiling Reveals Genes Involved in the Regulation of Wool Follicle Bulb Regression and Regeneration in Sheep
- Keratin disorders: from gene to therapy
- Prevalence and associated factors of skin diseases in aged nursing home residents: a multicentre prevalence study
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- Disorders of Keratinization
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- Keratin gene mutations in disorders of human skin and its appendages
- Genetics
- DERMATOLOGIC DISEASES AND PROBLEMS OF WOMEN THROUGHOUT THE LIFE CYCLE
- Skin, Genetic Defects, and Aging
- Sarcoidosis: Are there differences in your skin of color patients?
- Key Factors in the Complex and Coordinated Network of Skin Keratinization: Their Significance and Involvement in Common Skin Conditions
- Secondary cicatricial and other permanent alopecias
- Learning from nudity: lessons from the nude phenotype
- The Spectrum of Skin Disease Among Indian Children
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Hair Shaft Dysplasias
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- Transgenic Kallikrein 14 Mice Display Major Hair Shaft Defects Associated with Desmoglein 3 and 4 Degradation, Abnormal Epidermal Differentiation, and IL-36 Signature
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation
- Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- Poster Presentations at the 28th Joint Meeting of the International Society of Dermatopathology, March 5–6, 2025, Orlando, Florida, USA