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Research 661–690 of 1000+
- Systematized Epidermal Nevus with Epidermolytic Hyperkeratosis Improving with Topical Calcipotriol/Betametasone Dipropionate Combination Ointment
- Intracorneal vacuoles in skin diseases with parakeratotic hyperkeratosis in the dog: a retrospective light‐microscopy study of 111 cases (1973–2000)
- A Rare Case of Orthokeratotic Hyperkeratosis in a Kid Induced by Malassezial Dermatitis
- Multiple minute digitate hyperkeratosis
- Role of cholesterol sulfate in epidermal structure and function: Lessons from X-linked ichthyosis
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- A null mutation in the cystatin M/E gene of ichq mice causes juvenile lethality and defects in epidermal cornification
- Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3
- Epidermal Dysplasia and Abnormal Hair Follicles in Transgenic Mice Overexpressing Homeobox Gene MSX-2
- Ichthyosis with confetti: clinics, molecular genetics and management
- Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes
- Zinc‐responsive dermatosis in goats suggestive of hereditary malabsorption: two field cases
- Cutaneous adverse effects of BRAF inhibitors in metastatic malignant melanoma, a prospective study in 20 patients.
- Cutaneous Ultrastructural Features of the Flaky Skin (<i>fsn</i>) Mouse Mutation
- Monilethrix: a keratin hHb6 mutation is co‐dominant with variable expression
- Monilethrix treated with oral retinoids
- Nagashima-Type Palmoplantar Keratosis: A Common Asian Type Caused by SERPINB7 Protease Inhibitor Deficiency
- Leflunomide for the treatment of trichodysplasia spinulosa in a liver transplant recipient
- Perforating folliculitis with jaundice in an Indian male: a rare case with sclerosing cholangitis
- Symmetrical acrokeratoderma: A peculiar entity in China? Clinicopathologic and immunopathologic study of 34 new cases
- Characterizing Disease Features and Other Medical Diagnoses in Patients With Pityriasis Rubra Pilaris
- Two familial cases of Olmsted-like syndrome with a G573V mutation of the<i>TRPV3</i>gene
- Casts and pseudocasts
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Ichthyosis with confetti: a rare diagnosis and treatment plan
- Lichen Planopilaris is a Common Scarring Alopecia among Iraqi Population
- Sebaceous carcinoma arising at a chronic candidiasis skin lesion of a patient with keratitis-ichthyosis-deafness (KID) syndrome
- Monilethrix
- Corkscrew hairs
- Erythrokeratodermia Variabilis