Search
for
Sort by
Research 391–420 of 1000+
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- Actinic Hyperkeratosis Treated with Retinol Combined with a Polylysine Biovector: A Case Report
- Actinic Hyperkeratosis Treated with Retinol Combined with A Polylysine Biovector: A Case Report
- 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
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Role of cholesterol sulfate in epidermal structure and function: Lessons from X-linked ichthyosis
- Activation of Nrf2 in keratinocytes causes chloracne (MADISH)‐like skin disease in mice
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Reversing wrinkled skin and hair loss in mice by restoring mitochondrial function
- 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
- Trichoscopy
- 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 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
- Topically Applied Tretinoin in the Treatment of Trichostasis Spinulosa
- Nagashima-Type Palmoplantar Keratosis: A Common Asian Type Caused by SERPINB7 Protease Inhibitor Deficiency
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin 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