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Research 331–360 of 1000+
- Keratinisation status and cytokeratins of the human Meibomian gland epithelium
- Encephalocraniocutaneous lipomatosis: congenital alopecia treatment in a rare neurocutaneous syndrome
- Identification of Somatic <i>KRAS</i> Mutation in a Korean Baby with Nevus Sebaceus Syndrome
- Clinical Features and Treatment Options of Vogt-Koyanagi-Harada Disease
- Dilated tonic pupils with tabes dorsalis in neurosyphilis as first manifestation of HIV/AIDS: a video report
- Vogt-Koyanagi-Harada Disease with Oral Manifestations: A Rare Case Report
- 882 Syndactyly type III and hypotrichosis in oculodentodigital syndrome with GJA1 mutation
- The Pharma Market as Reflected by Patents
- More Yellow Ovaries
- Hormesis and medicine
- Advances in Chitosan-Based Nanoparticles for Drug Delivery
- Coronal approach for rehabilitative orbital decompression in Graves' ophthalmopathy
- Clinical development and management of adverse events associated with FGFR inhibitors
- Epidermal Nevi
- Meibomian gland changes in the rhino (hrrhhrrh) mouse.
- Calcitonin gene‐related peptide (CGRP) may award relative protection from interferon‐γ‐induced collapse of human hair follicle immune privilege
- Effects of Fetal Exposure to Diazoxide in Man
- Ectodermal Dysplasia: Otolaryngologic Manifestations and Management
- Applications of steroid drugs entrapped in cyclodextrins
- Regression of Pathologic Changes Induced by the Long-term Administration of Contraceptive Steroids to Rodents
- Applications of Nanostructured Lipid Carriers: Recent Advancements and Patent Review
- Bilateral circumscribed haemangioma of the choroid not associated with systemic vascular syndrome
- Matrigel uses in cell biology and for the identification of thymosin β4, a mediator of tissue regeneration
- Surgical Treatment of the Brow and Upper Eyelid
- Platelet lysate: a promising candidate in regenerative medicine
- Abnormal Saccadic Oscillations Associated with Severe Acute Respiratory Syndrome Coronavirus 2 Encephalopathy and Ataxia
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Advances in clinical applications of microneedle
- Hereditary Mucoepithelial Dysplasia and Autosomal-Dominant IFAP Syndrome Is a Clinical Spectrum Due to SREBF1 Variants
- Periocular Manifestations of Afatinib Therapy