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Research 421–450 of 1000+
- Spiny Keratoderma
- Keratosis pilaris
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report
- Pathogenesis of androgenetic alopecia
- Molecular Mechanisms Regulating Hair Follicle Development
- Transgenic Kallikrein 14 Mice Display Major Hair Shaft Defects Associated with Desmoglein 3 and 4 Degradation, Abnormal Epidermal Differentiation, and IL-36 Signature
- A combination of low-dose systemic etretinate and topical calcipotriol/betamethasone dipropionate treatment for hyperkeratosis and itching in Olmsted syndrome associated with a TRPV3 mutation
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- CPC14 Blaschko-linear trichoepitheliomas: unveiling type 1 segmental mosaicism
- Female Androgenetic (?) Alopecia
- RSPO1-mutated keratinocytes from palmoplantar keratoderma display impaired differentiation, alteration of cell–cell adhesion, EMT-like phenotype and invasiveness properties: implications for squamous cell carcinoma susceptibility in patients with 46XX disorder of sexual development
- Approach to Investigation of Hyperandrogenism in a Postmenopausal Woman
- Deficient anterior pituitary with common variable immune deficiency (DAVID syndrome): a new case and literature reports
- Six Novel Susceptibility Loci for Early-Onset Androgenetic Alopecia and Their Unexpected Association with Common Diseases
- Disorders of Keratinization
- Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma
- Th,-e mechanistic insights into the application of retinoids and possible adjunct therapeutic treatment to androgenic alopecia
- The Role of Interferon-γ in Autoimmune Polyendocrine Syndrome Type 1
- Male-pattern hair loss: Comprehensive identification of the associated genes as a basis for understanding pathophysiology
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Managing Cutaneous Manifestations of Hyperandrogenic Disorders
- Keratins: the hair shaft's backbone revealed
- Dermoscopy: A rapid bedside tool to assess monilethrix
- Congenital atrichia associated with situs inversus and mesocardia
- Research progress in the treatment of non-scarring alopecia: mechanism and treatment
- Poster presentationsSG11 KRT14 pathogenic or likely pathogenic variants beyond epidermolysis bullosa: dermatopathia pigmentosa reticularis
- Coexisting trichorrhexis nodosa and pili annulati: a case report of hair shaft abnormalities in a syrian family
- Porphyria Cutanea Tarda – a Case Report