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Research 421–450 of 749
- UTILIZAÇÃO DE ISOTRETINOÍNA ORAL NO TRATAMENTO DA ALOPECIA FIBROSANTE FRONTAL: SÉRIE DE CASOS
- UTILIZAÇÃO DE ISOTRETINOÍNA ORAL NO TRATAMENTO DA ALOPECIA FIBROSANTE FRONTAL: SÉRIE DE CASOS
- Foam - rediscovered drug form
- Poster session
- National scientific medical meeting 1996 abstracts
- A Novel Technique for Repositioning Lower Eyelid Fat via the Transoral Approach in Association with Midface Lift
- Ichthyosis
- Corneodesmosomes and corneodesmosin: from the stratum corneum cohesion to the pathophysiology of genodermatoses
- Cutaneous Adnexal Cysts Revisited: What We Know and What We Think We Know
- Mechanotransductive Differentiation of Hair Follicle Stem Cells Derived from Aged Eyelid Skin into Corneal Endothelial-Like Cells
- Molluscum Contagiosum in an Epidermoid Cyst
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- Amplitude-guided deep reinforcement learning for semi-supervised layer segmentation
- The pattern recognition receptor toll-like receptor 3 regulates skin barrier homeostasis
- The fatty acids and the skin: a focus on the n-6 family of unsaturated fatty acids
- Study of thin films and nanoparticles obtained by self-assembly of block copolymers and their interactions with an oligo / polysaccharide
- Etude de films minces et de nanoparticules obtenus par auto-assemblage de copolymères à blocs et leurs interactions avec un oligo/polysaccharide
- Porokeratotic Eccrine Ostial and Dermal Duct Nevus: A Report of Rare Late-Onset Solitary Lesion
- Three-dimensional microanatomy of mechanoreceptors and their possible mechanism of sensory transduction.
- Extensive Spiculated Follicular Porokeratosis With Alopecia: A Case Report
- Spink5-deficient mice mimic Netherton syndrome through degradation of desmoglein 1 by epidermal protease hyperactivity
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Dermal white adipose tissue: a new component of the thermogenic response
- In situ tensile deformation characterization of human hair with atomic force microscopy
- Isolation and Characterization of Human Repetin, a Member of the Fused Gene Family of the Epidermal Differentiation Complex
- Netherton syndrome subtypes share IL-17/IL-36 signature with distinct IFN-α and allergic responses
- Disorders of Keratinization
- Contribution of the Hair Follicular Pathway to Total Skin Permeation of Topically Applied and Exposed Chemicals
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Distinguishing Mouse Strains by Proteomic Analysis of Pelage Hair