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Research 241–270 of 784
- Dynamics of Hair Follicle Morphogenesis and Skin Homeostasis
- British Society for Paediatric Dermatology Annual Meeting, Sheffield, 18-19 November 2016
- A polarizing light microscopy can be an easy and reliable diagnostic tool of congenital keratinizing disorders including Netherton syndrome
- Skin, Genetic Defects, and Aging
- Clinical Snippets
- Steroid Sulfatase: Molecular Biology, Regulation, and Inhibition
- Human stratum corneum proteomics reveals cross‐linking of a broad spectrum of proteins in cornified envelopes
- Roles of steroid sulfatase in brain and other tissues
- Genetic Mapping Of Hereditary Ectodermal Dysplasias And Hair Loss Genes
- New clinico‐genetic classification of trichothiodystrophy
- Case Report of Wound Treatment with Hyiodine Gel in an Occasional KID Syndrome Patient
- Novel Mutations in X-Linked Dominant Chondrodysplasia Punctata (CDPX2)
- From molecular biology to therapeutics
- Oral retinoids-present status
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- Viva questions from the IJDVL
- Netherton Syndrome
- 075 Clinical investigation of JAK inhibitor Tofacitinib in scarring alopecias
- Vitamins
- Three-Dimensional Analysis of Cell Division Orientation in Epidermal Basal Layer Using Intravital Two-Photon Microscopy
- Thyroid hormone action on skin.
- Secondary cicatricial and other permanent alopecias
- Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain
- Localisation and regulation of cholesterol transporters in the human hair follicle: mapping changes across the hair cycle
- Spectrum of mucocutaneous manifestations in human immunodeficiency virus-infected patients and its correlation with CD4 lymphocyte count
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- Frontal fibrosing alopecia
- Hair loss
- Psoriatic Alopecia
- Dupilumab in a 9-week-old with Netherton Syndrome Leads to Deep Symptom Control