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Research 931–960 of 996
- A rash diagnosis
- Soft Tissue Augmentation of the Temporal Brow in Browlifting Surgery
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Successful treatment of corticosteroid-resistant ophiasis-type alopecia areata (AA) with platelet-rich plasma (PRP)
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Clinical, biochemical and mutational findings in biotinidase deficiency among Malaysian population
- Adverse Reaction to Cetuximab, an Epidermal Growth Factor Receptor Inhibitor.
- Seborrheic Dermatitis Revisited: Pathophysiology, Diagnosis, and Emerging Therapies—A Narrative Review
- Medical, dental and dual-degree ‘Oral-Maxillofacial’ signatures — what have I seen over the past 22 years?
- Differential Diagnosis of Headache and Vertigo: Topical Minoxidil Self-medication Should Be Considered
- Understanding the safety profile of topical minoxidil: a retrospective review
- Dietary Influences on Skin Health in Common Dermatological Disorders
- Lupus Erythematosus Profundus with Multiple Overlying Cutaneous Ulcerations: A Rare Case
- Extrapulmonary manifestations of coronavirus disease (COVID-19): current status (a literature review)
- A syndrome of congenital ichthyosis, mental retardation, myopathy and anemia in dizygotic twin sisters
- Angiogenesis: a Dynamic Balance of Stimulators and Inhibitors
- The Rotterdam Study: 2010 objectives and design update
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- COVID-19: Pulmonary and Extra Pulmonary Manifestations
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
- Expression of truncated latent TGF-β-binding protein modulates TGF-β signaling
- Androgenetic alopecia and coronary artery disease in women
- Molecular–clinical correlations in a family with variable tissue mitochondrial DNA T8993G mutant load
- Feasibility of repairing full-thickness skin defects by iPSC-derived epithelial stem cells seeded on a human acellular amniotic membrane
- Functionally enhanced placenta-derived mesenchymal stem cells inhibit adipogenesis in orbital fibroblasts with Graves’ ophthalmopathy
- Induced pluripotent stem cells from human hair follicle keratinocytes as a potential source for <i>in vitro</i> hair follicle cloning
- Therapeutic effects of stem cells in different body systems, a novel method that is yet to gain trust: A comprehensive review