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Research 631–660 of 740
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Use of Contact Immunotherapy in the Treatment of Skin Diseases Other than Alopecia Areata
- Generalized multiple eruptive milia in an infant – An unusual presentation
- Schmallenberg virus infection suspected in a calf born to an imported heifer
- Clinical Role of Oral Vitamin C and E Therapy in Skin and Hair Disorders
- SnapshotDx Quiz: May 2020
- 022 Randomized, double-blind, placebo-controlled, single-centre, phase I safety study of intradermal injections of autologous fibroblasts isolated from the non-bulbar dermal sheath of the hair follicle to treat skin aging
- Cells, growth factors and biomaterials used in tissue engineering for hair follicles regeneration
- Cells and Structures Involved in Hair Follicle Regeneration: An Introduction
- Anticonvulsant-Induced Cutaneous Reactions
- Angiogenic effects of recombinant thymosin β4 in a mouse hindlimb ischemia model
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Essential Role of STAT3 Signaling in Hair Follicle Homeostasis
- Systematized Epidermal Nevus with Epidermolytic Hyperkeratosis Improving with Topical Calcipotriol/Betametasone Dipropionate Combination Ointment
- Missense mutation Y449H of the K10 gene in a patient with severe epidermolytic ichthyosis
- Case of epidermolytic ichthyosis (bullous congenial ichthyosiform erythroderma) with a novel L157P mutation in KRT10 complicated by hypercalcemia
- Superficial Epidermolytic Ichthyosis—Hypertrichosis as a Clue to Diagnosis
- Toxic epidermal necrolysis caused by etonogestrel implantation: A rare presentation
- Inherited disorders of the skin in human and mouse: from development to differentiation.
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- A newborn presenting with congenital blistering
- British Society for Paediatric Dermatology Annual Meeting, Sheffield, 18-19 November 2016
- Cutaneous manifestations of the COVID-19 pandemic in schoolchildren and adolescents
- Research Snippets
- BULLOUS LUPUS, AN UNCOMMON CAUSE OF ATYPICAL ESOPHAGITIS: A CASE REPORT
- KRT16 wt Allele
- 075 Clinical investigation of JAK inhibitor Tofacitinib in scarring alopecias
- Toxic Epidermal Necrolysis
- Severe cutaneous adverse reactions to drugs
- Improving Posttraumatic Facial Scars