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Research 61–90 of 1000+
- Clinical Manifestation and Classification of Japanese patients with Inherited Keratinizing Disorders
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- Skin barrier, phenotypic and genotypic characterisation of autosomal recessive ichthyosis in TGM1‐deficient Jack Russell Terriers and response to topical ceramide
- PHILADELPHIA DERMATOLOGICAL SOCIETY
- Uso actual de la vitamina D en dermatología
- Chemotherapy of psoriasis and other skin disorders with oral retinoids
- Primary cicatricial alopecias
- Alopecia patterns and trichoscopic findings in patients with autosomal recessive congenital ichthyosis
- Existence of trichohyalin-keratohyalin hybrid granules: Co-localization of two major intermediate filament-associated proteins in non-follicular epithelia
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- PA11 A rare case of a severe papulopustular dermatosis secondary to a germline <i>EGFR</i> mutation
- Generalized Asymptomatic Cutaneous Pits and Comedones in a Young Woman
- Circle Hairs in a Patient with Multiple Myeloma
- Graham‐Little Piccardi Lassueur syndrome and review of the literature
- Graham-Little Piccardi Lassueur Syndrome and review of the literature
- Commentary: Darier-White Disease
- Asebia-2J (Scd1ab2J): A New Allele and a Model for Scarring Alopecia
- Changing Patterns of Localization of Putative Stem Cells in Developing Human Hair Follicles
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Madarosis: A marker of many Maladies
- Hair follicles modulate skin barrier function
- Putting the Human Hair Follicle Cycle on the Map
- Trichothiodystrophy without associated neuroectodermal features in two siblings
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Circle hairs involving the extremities in a young girl
- A Comprehensive Review: The Bidirectional Role of Sebum in Skin Health
- Miscellaneous Skin Diseases
- Keratosis Pilaris-like Eruption during Treatment of Chronic Myeloid Leukemia with Tyrosine Kinase Inhibitors: Literature Review and Report of a Case Related to Imatinib
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis