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Research 511–540 of 1000+
- 54269 Patchy hair loss, hyperpigmented plaques, and hyperkeratotic papules in a middle aged woman
- 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
- 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
- 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