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Research 91–120 of 1000+
- Proceedings of the Ninth World Congress for Hair Research (2015)
- WNT Signaling in Disease
- TRP Channels in Skin Biology and Pathophysiology
- Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis
- Keratins and skin disease
- Genetics of Inherited Ichthyoses and Related Diseases
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Genetic Hair Disorders: A Review
- 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
- New developments in the molecular treatment of ichthyosis: review of the literature
- Hidradenitis Suppurativa and Comorbid Disorder Biomarkers, Druggable Genes, New Drugs and Drug Repurposing—A Molecular Meta-Analysis
- Hair shaft disorders in children – An update
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Botulinum Toxins in Medical and Cosmetic Dermatology
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- A guide to diagnosis and management of hypertrichosis
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review
- EBS in Children with De Novo Pathogenic Variants Disturbing Krt14
- Dermatologic manifestations of thyroid disease: a literature review
- The Non-Cosmetic Dermatological Use of Botulinum Neurotoxin
- [Translated article] Keys to the Diagnosis of Hair Shaft Disorders: Part II
- Circle Hairs in a Patient with Multiple Myeloma
- Subject Index
- TONGUE, RED
- Protein profiling of forehead epidermal corneocytes distinguishes frontal fibrosing from androgenetic alopecia
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report