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Research 661–690 of 1000+
- Author Index
- Spiny Hyperkeratotic Projections on the Face and Extremities of a Kidney Transplant Recipient—Quiz Case
- Keratin pattern in hyperkeratotic and ulcerated gastric pars oesophagea in pigs
- A combination of low-dose systemic etretinate and topical calcipotriol/betamethasone dipropionate treatment for hyperkeratosis and itching in Olmsted syndrome associated with a TRPV3 mutation
- Resolution of the plantar hyperkeratosis of pachyonychia congenita during chemotherapy for Ewing sarcoma
- Pruritic Hyperkeratotic Facial Papules
- An Unusual Case of Tinea Capitis Presented as Erythematous, Hyperkeratotic, Scaly Plaque with Alopecia
- Zinc-responsive Acral Hyperkeratosis as a Sequele of Acrodermatitis Enteropathica
- Loss of Keratin K2 Expression Causes Aberrant Aggregation of K10, Hyperkeratosis, and Inflammation
- [Dermatophytic disease: exuberant hyperkeratosis with cutaneous horns].
- 738 Cryo-EM and molecular dynamics of TRPV3 channel in activated state reveal structural features implicated in severe itch and hyperkeratosis
- Unilateral nevoid hyperkeratosis of the nipple and areola in a Saudi female
- <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
- Multiple minute digitate hyperkeratosis
- 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
- 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
- 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