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Research 751–780 of 1000+
- Potential Cosmetic Applications of Dihydroartemisinin
- A scientometric study on research trends and characteristics of discoid lupus erythematosus
- Dermatoses in Postmenopausal Women in a Tertiary Health Care Center of Bihar: A Prospective Cross-Sectional Study
- Porokeratotic Eccrine Duct and Hair Follicle Nevus (PEHFN) Associated with Keratitis-Ichthyosis-Deafness (KID) Syndrome
- Efficacy and Safety of Long-Pulsed 755-nm Alexandrite Laser for Keratosis Pilaris: A Split-Body Randomized Clinical Trial
- Optical coherence tomography-assisted diagnosis of follicular keratosis of the chin
- <i>Malassezia</i> Display a Hyphae-like “Spaghetti-and-Meatballs” Configuration in Keratotic Plugs
- Keratosis Follicularis Squamosa in Unilateral Buttock: A Case Report and Review of Literature in China
- 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: 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
- 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
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- Keratosis Follicularis Spinulosa Decalvans. What Syndrome Is This?
- 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.