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Research 211–240 of 279
- Nutrition and Hair Anomalies
- Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss
- Érythrodermies néonatales et infantiles : apport de la biopsie cutanée précoce dans les formes graves
- 305 Overlaps between inflammatory dermatoses and ichthyoses: need for novel therapeutic approaches
- Genetics of Alopecia
- [Black piedra in South Africa. 1st description in a child with bamboo hair, pili torti and congenital erythroderma ichthyosiforme].
- Ichthyosis with confetti: clinics, molecular genetics and management
- Body mass index across development and adolescent hair cortisol: the role of persistence, variability, and timing of exposure
- New developments in the molecular treatment of ichthyosis: review of the literature
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Nonscarring alopecia associated with vitamin D deficiency.
- A Systematic Review of Endocrine Therapy for Improved Reproductive and Metabolic Outcomes in PCOS Women
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- In vivo reflectance confocal microscopy: usefulness for diagnosing hair diseases
- Vitamin D and the Skin: A Review for Dermatologists
- Genetic Control/Involvement in Hair Fiber Traits
- Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report
- Advances in the treatment of autosomal recessive congenital ichthyosis, a look towards the repositioning of drugs
- Complex Extract of Polygonatum sibiricum and Nelumbinis semen Improves Menopause Symptoms via Regulation of Estrogen Receptor Beta in an Ovariectomized Rat Model
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Eyebrow Loss
- Cell death in skin function, inflammation, and disease
- The genetics of alopecia areata: New approaches, new findings, new treatments
- Author Index
- Proteome Analysis of Human Hair Shaft
- Delineation of Matriptase Protein Expression by Enzymatic Gene Trapping Suggests Diverging Roles in Barrier Function, Hair Formation, and Squamous Cell Carcinogenesis
- Disorders of Keratinization
- Nagashima-Type Palmoplantar Keratosis: A Common Asian Type Caused by SERPINB7 Protease Inhibitor Deficiency
- Key Factors in the Complex and Coordinated Network of Skin Keratinization: Their Significance and Involvement in Common Skin Conditions