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Research 31–60 of 1000+
- A Randomised-Controlled Study Demonstrates That Diet Can Contribute to the Clinical Management of Feline Atopic Skin Syndrome (FASS)
- Hair Loss in Children
- Inherited Epidermolysis Bullosa: A Clinical Case
- Clinical Snippets
- Efficacy of Dupilumab in Treating Atopic Dermatitis With Recurrent Eczema Herpeticum in a Patient With DOCK8-Deficiency Hyper-IgE Syndrome: A Case Report
- Cutaneous Lesions in Systemic Lupus Erythematosus
- Recombinant Thrombomodulin Used to Successfully Treat Cronkhite-Canada Syndrome with Disseminated Intravascular Coagulation due to Sepsis in a Compromised Patient
- Skin Manifestations of Rheumatological Diseases
- General Characteristics of Hair in Eating Disorders
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- A Case Report of Cronkhite-Canada Syndrome Complicated by Membranous Nephropathy
- Dermatologic Conditions of the Early Post-Transplant Period in Hematopoietic Stem Cell Transplant Recipients
- Trichodystrophies: A hair-raising differential diagnosis
- Management of congenital ichthyoses: European guidelines of care, part two
- Chemotherapy and Cutaneous Drug Reactions
- Hypotrichosis in a child with olmsted syndrome
- Appearance and Internal Aging
- Update on Hidradenitis Suppurativa (Part I): Epidemiology, Pathogenesis, Severity assessment and Comorbidities
- Skin as a Metabolic Organ: Dermatologic Markers of Morbid Obesity and Their Role in Risk Stratification and Treatment Monitoring
- Expanding the Cutaneous Spectrum of Nicolaides‑Baraitser Syndrome: Eczema and Generalized Hair Loss
- Book Reviews
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- The Fate of Epidermal Tight Junctions in the stratum corneum: Their Involvement in the Regulation of Desquamation and Phenotypic Expression of Certain Skin Conditions
- Dupilumab in Inflammatory Skin Diseases: A Systematic Review
- Hidradenitis Suppurativa
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- Severe Monilethrix Associated with Intractable Scalp Pruritus, Posterior Subcapsular Cataract, Brachiocephaly, and Distinct Facial Features: A New Variant of Monilethrix Syndrome?
- Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex
- PA11 A rare case of a severe papulopustular dermatosis secondary to a germline <i>EGFR</i> mutation
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency