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Research 361–390 of 1000+
- Clinico-epidemiology of Keratosis Pilaris with Histopathologic and Dermoscopic Evaluation – A Cross-sectional Study in a Rural Tertiary Hospital
- 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
- Follicular keratotic diseases: a retrospective study of 50 cases in a tertiary care center of rural South India with dermoscopy and histopathology evaluation
- 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
- A Rare Case of Keratosis Follicularis Spinulosa Decalvans Affecting a Female Child
- Keratosis pilaris with adjacent haemosiderin deposition: a clue to scurvy
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Clinical Findings, Cutaneous Pathology, and Response to Therapy in 21 Patients With Keratosis Pilaris Atrophicans
- Keratosis Follicularis Spinulosa Decalvans
- Keratosis follicularis spinulosa decalvans: a family study of seven male cases and six female carriers.
- Keratosis follicularis spinulosa decalvans and acne keloidalis nuchae
- Keratosis Follicularis Spinulosa Decalvans Associated with Acne Keloidalis Nuchae and Tufted Hair Folliculitis
- 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
- 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
- Nilontinib induced keratosis pilaris atrophicans
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- Eyebrow reconstruction in dormant keratosis pilaris atrophicans
- Keratosis Follicularis Spinulosa Decalvans. What Syndrome Is This?
- KERATOSIS FOLLICULARIS WITH UNUSUAL INVOLVEMENT OF THE SCALP
- 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