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Research 31–60 of 1000+
- The overview of the cosmetic exfoliants composition for keratosis pilaris skincare
- Clinico-epidemiology of Keratosis Pilaris with Histopathologic and Dermoscopic Evaluation – A Cross-sectional Study in a Rural Tertiary Hospital
- Presentations of Cutaneous Disease in Various Skin Pigmentations: Keratosis Pilaris
- Efficacy and safety of the Exfoliate-Dissolve-Repair skin care approach in the treatment of keratosis pilaris: a randomized controlled clinical trial study protocol
- Homoeopathic management of keratosis pilaris with Arsenic Album: A case report
- The Effectiveness of Topical Keratolytics (Alpha Hydroxy Acids/Beta Hydroxy Acids/Urea) in Treating Keratosis Pilaris: A Review of the Literature
- An Innovative Formula for Keratosis Pilaris Treatment—A Randomized Controlled Study Based on the “Exfoliation‐Dissolution‐Repair” Concept
- Navigating Diagnostic Uncertainty: Frontal Fibrosing Alopecia Versus Keratosis Pilaris Atrophicans Faciei With Genetic Testing Insights
- Keratosis Follicularis Squamosa in Unilateral Buttock: A Case Report and Review of Literature in China
- Keratosis Pilaris-like Eruption during Treatment of Chronic Myeloid Leukemia with Tyrosine Kinase Inhibitors: Literature Review and Report of a Case Related to Imatinib
- Clinicopathologic and trichoscopic features of keratosis follicularis spinulosa decalvans: A case series study
- Keratosis Pilaris Is a Keratinization of Hair Follicles
- A Rare Case of Keratosis Follicularis Spinulosa Decalvans Affecting a Female Child
- Keratosis pilaris with adjacent haemosiderin deposition: a clue to scurvy
- Ulerythema ophryogenes (keratosis pilaris atrophicans faciei).
- Keratosis Follicularis
- [Electrophoretic studies of acid mucopolysaccharides in skin, prekeratin of hair follicles and in keratoses of wool].
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- A novel mutation in the connexin 26 gene (<i>GJB2</i>) in a child with clinical and histological features of keratitis–ichthyosis–deafness (KID) syndrome
- Severe form of keratitis–ichthyosis–deafness (KID) syndrome associated with septic complications
- Porokeratotic Eccrine Duct and Hair Follicle Nevus (PEHFN) Associated with Keratitis-Ichthyosis-Deafness (KID) Syndrome
- Identification of compound heterozygous mutations in <i>AP1B1</i> leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome
- Connexin 26 (<i>GJB2</i>) mutations in keratitis–ichthyosis–deafness syndrome presenting with squamous cell carcinoma
- Keratinisation status and cytokeratins of the human Meibomian gland epithelium
- Episodes of Keratitis during Treatment with Baricitinib for Alopecia Areata
- Overexpression of HE4/WFDC2 gene in mice leads to keratitis and corneal opacity
- Keratitis-Ichthyosis-Deafness Syndrome Caused by Missense Mutation in GJB2 Encoding Connexin 26 in a Chinese Patient
- Actinic keratosis: a clinical and epidemiological revision
- Field Cancerization: From Molecular Basis to Selective Field-Directed Management of Actinic Keratosis
- Seborrheic keratosis