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Research 181–210 of 367
- 554 Repurposing a clinical antimalarial for the therapeutic induction of lethal ER stress targeting BRAF-kinase inhibitor-resistant malignant melanoma
- 556 α 1 -AR agonist induced piloerection protects against the development of traction alopecia
- 557 A peptide derivative with known anti-wrinkle properties was identified as potent dipeptiylpeptidase-4 inhibitor
- Fondation René Touraine
- Clinical Management in Psychodermatology
- Tricotiodistrofia. Reporte de un caso
- Dermatology
- Poster session
- 600 Differential Molecular Signature of Dermal Papilla Cells (DPCs) from Balding and Non balding Scalp in 2D, 3D culture and Co-culture with Adipose-derived stem cells (ASCs)
- Issue Information - TOC
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Unveiling the Potential of Dermoscopy in Diagnosing Netherton Syndrome
- Successful management of Netherton syndrome using IVIG and dupilumab: A case report
- Familial Dyskeratotic Comedones: A Case Report and Literature Review
- Beyond Coincidence in Neurofibromatosis Type 1: Becker Nevus Adjacent to Plexiform Neurofibroma with Brachial Plexus Involvement and Integrated Mechanistic Illustration
- Successful Management of Netherton Syndrome Using IVIG and Dupilumab: A Case Report
- Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review
- Activated Kras Alters Epidermal Homeostasis of Mouse Skin, Resulting in Redundant Skin and Defective Hair Cycling
- 557 Short-term Rho-associated kinase inhibitor treatment accelerates primary keratinocyte growth without affecting the characteristics of the stem cell population
- Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3
- SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature
- Netherton Syndrome With Trichorrhexis Invaginata “Bamboo Hair” Under Dermoscopy: Case Images
- [Monilethrix is a hereditary hair shaft disorder].
- A rare hair loss in children: Monilethrix
- Muir-torre syndrome in two families in Leicestershire, United Kingdom
- Increased risk of chronic fatigue and hair loss following COVID-19 in individuals with hypohidrotic ectodermal dysplasia
- 092 Novel biallelic RIPK4 mutations cause ectodermal dysplasia with cutaneous syndactyly
- Ichthyosis with confetti: clinics, molecular genetics and management
- Pachyonychia Congenita-Associated Alopecia. A Microscopic Analysis Using Transverse Section Technique