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Research 121–150 of 1000+
- Frontal Fibrosing Alopecia Involving the Limbs Shows Inflammatory Pattern on Histology: A Review of 13 Cases
- Prognosis and outcomes of forelimb amputation in two raccoon dogs
- Quality of life case series review: wound bed preparation from a UK perspective
- A 36-Year-Old Woman With an Unexpected Cause of Hypokalemia
- Poster Abstracts
- A case report and brief literature review of Klippel-Trénaunay syndrome
- The Effects of Vascular Tissue Transplantation and Anastomosis at Different Storage Time Periods on Tissue Repair in a Rat Ischemia Model
- Diffuse hypertrichosis during treatment with 5% topical minoxidil
- Effect of Platelet Rich Fibrin on Wound Healing Time after Revascularization
- Stabilization of β-catenin promotes melanocyte specification at the expense of the Schwann cell lineage
- The effects of sonic, desert and Indian hedgehog signalling in skin
- The use of a retinoid receptor antagonist in a new model to study vitamin A-dependent developmental events.
- Acute hair loss on the limbs in frontal fibrosing alopecia: a clinicopathological study of two cases
- Cell Cycle Regulation and Regeneration
- THALLIUM POISONING
- Expression of the Scube3 epidermal growth factor-related gene during early embryonic development in the mouse
- Lipodermatosclerosis: a postphiebitic syndrome
- Characterization of a mouse Scube3 reporter line
- Case Report of Wound Treatment with Hyiodine Gel in an Occasional KID Syndrome Patient
- A case of multifocal acquired demyelinating sensory and motor neuropathy with whole body alopecia
- Atypical Presentation of Systemic Lupus Erythematous with Vasculitic Polyneuropathy
- Progressive Motor Regression in a 3-Year-Old: Dietary Trends Revive an Overlooked Diagnosis
- Roles for Msx and Dlx homeoproteins in vertebrate development
- Hyperaldosteronism and Hyperprogesteronism in a Cat
- Novel Mutations in X-Linked Dominant Chondrodysplasia Punctata (CDPX2)
- Lucio Phenomenon: Sequelae of Neglected Leprosy
- Porokeratotic eccrine ostial and dermal duct nevus: A noteworthy presentation
- Mitochondrial DNA 10158T>C mutation in a patient with mitochondrial encephalomyopathy with lactic acidosis, and stroke-like episodes syndrome
- Localized Primary Cutaneous Nodular Amyloidosis in a Patient With Paraproteinemia
- Improvement of Skin Lesions in an Adult with CHILD Syndrome Treated with 2% Ketoconazole Cream