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Research 691–720 of 1000+
- Perceived Stigmatization among Dermatological Outpatients Compared with Controls: An Observational Multicentre Study in 17 European Countries
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- Widespread porokeratotic adnexal ostial nevus: Clinical features and proposal of a new name unifying porokeratotic eccrine ostial and dermal duct nevus and porokeratotic eccrine and hair follicle nevus
- Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy
- Pseudoxanthoma Elasticum: Progress in Research Toward Treatment: Summary of the 2012 PXE International Research Meeting
- Nail changes in alopecia areata: an update and review
- Biotin Deficiency in an Infant Fed with Amino Acid Formula
- Trichoscopy as a clue to the diagnosis of scalp sarcoidosis
- Androgenetic alopecia in COVID-19: Compared to age-matched epidemiologic studies and hospital outcomes with or without the Gabrin sign
- Phenotypic variability associated with<i>WNT10A</i>nonsense mutations
- Skin diseases associated with hepatitis C virus: Facts and controversies
- Topically Applied Tretinoin in the Treatment of Trichostasis Spinulosa
- Nagashima-Type Palmoplantar Keratosis: A Common Asian Type Caused by SERPINB7 Protease Inhibitor Deficiency
- Implication of Human Bacterial Gut Microbiota on Immune-Mediated and Autoimmune Dermatological Diseases and Their Comorbidities: A Narrative Review
- Localized cutaneous necrosis associated with the antiphospholipid syndrome
- The Important Role of Leptin in Modulating the Risk of Dermatological Diseases
- Epidermolysis Bullosa Simplex Caused by Distal Truncation of BPAG1-e: An Intermediate Generalized Phenotype with Prurigo Papules
- ANTI‐HAIR KERATIN MONOCLONAL ANTIBODY (HKN‐2)
- Emulgel: A Novel Approach For Hydrophobic Drugs
- Polyglandular autoimmune syndrome type III with a prevalence of cutaneous features
- Selected variants of the melanocortin 4 receptor gene (MC4R) do not confer susceptibility to female pattern hair loss
- Exacerbation of systemic lupus erythematosus after receiving mRNA‐1273‐based coronavirus disease 2019 vaccine
- Skin and hair abnormalities of Cantu syndrome: A congenital hypertrichosis due to a genetic alteration mimicking the pharmacological effect of minoxidil
- Fibrosing Alopecia in a Pattern Distribution: A Case Report and Literature Review
- Chronic tophaceous gout secondary to self-induced vomiting in anorexia nervosa
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Alopecia Areata in an Adolescent With Inflammatory Bowel Disease
- Topically applied tretinoin in the treatment of trichostasis spinulosa
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Alopecia areata