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Research 301–330 of 1000+
- 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
- Keratosis follicularis spinulosa decalvans in a family
- Severe form of keratitis–ichthyosis–deafness (KID) syndrome associated with septic complications
- Treatment of Keratosis Pilaris With 810-nm Diode Laser
- Nilotinib-Induced Keratosis Pilaris
- Keratosis follicularis spinulosa decalvans in a female
- Connexin 26 (<i>GJB2</i>) mutations in keratitis–ichthyosis–deafness syndrome presenting with squamous cell carcinoma
- Nilontinib induced keratosis pilaris atrophicans
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- Sebaceous carcinoma arising at a chronic candidiasis skin lesion of a patient with keratitis-ichthyosis-deafness (KID) syndrome
- Eyebrow reconstruction in dormant keratosis pilaris atrophicans
- Keratosis Follicularis Spinulosa Decalvans. What Syndrome Is This?
- Efficacy and safety of non‐cross‐linked hyaluronic acid compound in the treatment of keratosis pilaris: A split‐body randomized clinical trial
- Substance P in keratosis follicularis spinulosa decalvans
- Mapping of a novel locus for keratosis follicularis squamosa on chromosome 7p14.3–7p12.1
- Unilateral keratosis pilaris atrophicans faciei mimicking follicular mucinosis
- Episodes of Keratitis during Treatment with Baricitinib for Alopecia Areata
- Keratosis pilaris
- Keratinic amyloid deposition in canine hair follicle tumors
- A toddler case of keratosis follicularis squamosa (Dohi) successfully treated with salicylic acid ointment
- Keratosis Follicularis Spinulosa Decalvans: Diagnosis and Therapeutic Evaluation.
- The overview of the cosmetic exfoliants composition for keratosis pilaris skincare
- Early removal of post-operative scabs after follicular unit extraction using a 2% salicylic acid keratolytic shampoo: a multicentre descriptive pilot study
- Presentations of Cutaneous Disease in Various Skin Pigmentations: Keratosis Pilaris
- An Innovative Formula for Keratosis Pilaris Treatment—A Randomized Controlled Study Based on the “Exfoliation‐Dissolution‐Repair” Concept
- Overexpression of HE4/WFDC2 gene in mice leads to keratitis and corneal opacity
- Navigating Diagnostic Uncertainty: Frontal Fibrosing Alopecia Versus Keratosis Pilaris Atrophicans Faciei With Genetic Testing Insights
- Clinicopathologic and trichoscopic features of keratosis follicularis spinulosa decalvans: A case series study
- Keratosis Pilaris Is a Keratinization of Hair Follicles
- Keratitis-Ichthyosis-Deafness Syndrome Caused by Missense Mutation in GJB2 Encoding Connexin 26 in a Chinese Patient