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Research 211–240 of 1000+
- Pretibial Pruritic Papular Dermatitis: A Case Report and Emphasis on Effective Treatment with Pentoxifylline
- Dermatologic manifestations of thyroid disease: a literature review
- Confocal microscopy and optical coherence tomography of inflammatory skin diseases in hairs and pilosebaceous units: A systematic review
- Recent Advances in Understanding of the Etiopathogenesis, Diagnosis, and Management of Hair Loss Diseases
- Hair Disorders in Autoimmune Diseases
- The spectrum of fibrosing alopecias
- Skin Manifestations of Rheumatological Diseases
- Oral Presentations
- Clinical Characteristics, Quality of Life, and Risk Factors of Amputation Stump Skin Disease and Stump Fungal Infection in Adult Amputees in Shanghai, China
- The Rotterdam Study: objectives and design update
- Adult female acne: a guide to clinical practice
- Unraveling the ECM-Immune Cell Crosstalk in Skin Diseases
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Histologic Changes in the Skin of Hairless Mice Following Peeling With Salicylic Acid
- Trichoscopy in genetic hair shaft abnormalities
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation
- Age-associated inflammation connects RAS-induced senescence to stem cell dysfunction and epidermal malignancy
- Hair Growth Defects in Insig-Deficient Mice Caused by Cholesterol Precursor Accumulation and Reversed by Simvastatin
- Molecular Genetics of the PI3K-AKT-mTOR Pathway in Genodermatoses: Diagnostic Implications and Treatment Opportunities
- Alginate-Based Composites for Corneal Regeneration: The Optimization of a Biomaterial to Overcome Its Limits
- Ribonucleotide Excision Repair Is Essential to Prevent Squamous Cell Carcinoma of the Skin
- Topical Administration of Drugs Incorporated in Carriers Containing Phospholipid Soft Vesicles for the Treatment of Skin Medical Conditions
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- Alopecia Areata: Pathogenesis, Diagnosis, and Therapies
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- The Important Role of Leptin in Modulating the Risk of Dermatological Diseases
- Beyond the Surface: Understanding Demodex and Its Link to Blepharitis and Facial Dermatoses
- Skin manifestations associated with systemic diseases – Part I
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Advancements in Dermatological Imaging Modalities