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Research 961–990 of 1000+
- MON-594 Alternating Hypothyroidism and Hyperthyroidism Complicated by Thyroid Eye Disease
- 54269 Patchy hair loss, hyperpigmented plaques, and hyperkeratotic papules in a middle aged woman
- Halting the Progression of Cicatricial Alopecia with Injectable Platelet-Rich Fibrin
- Case Report: 7 Year-Old Saudi Female with Monilethrix
- Lasers for Other Specific Dermatologic Disorders
- A rash diagnosis
- Review of Hair Removal in Traditional Medicine and Its Clinical Application
- Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome
- Clinical, biochemical and mutational findings in biotinidase deficiency among Malaysian population
- Two novel <i>BTD</i> mutations causing profound biotinidase deficiency in a Chinese patient
- Medical, dental and dual-degree ‘Oral-Maxillofacial’ signatures — what have I seen over the past 22 years?
- Vitiligo and Its Mimics in Childhood: A Diagnostic Framework for Hypopigmented Disorders
- Lupus Erythematosus Profundus with Multiple Overlying Cutaneous Ulcerations: A Rare Case
- A syndrome of congenital ichthyosis, mental retardation, myopathy and anemia in dizygotic twin sisters
- Angiogenesis: a Dynamic Balance of Stimulators and Inhibitors
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- 25 Years of Epidermal Stem Cell Research
- Progress in studies of epidermal stem cells and their application in skin tissue engineering
- Molecular–clinical correlations in a family with variable tissue mitochondrial DNA T8993G mutant load
- Loss of Msx2 Function Down-Regulates the FoxE3 Expression and Results in Anterior Segment Dysgenesis Resembling Peters Anomaly
- A rare case of woolly hair with unusual associations
- Morbihan disease and extrafacial lupus miliaris disseminatus faceie: a case report
- Tp63-expressing adult epithelial stem cells cross lineages boundaries revealing latent hairy skin competence
- Exploring the efficacy of baricitinib in treating alopecia areata after failed Janus kinase inhibitor therapy
- The Use of High-Density SNP Array to Map Homozygosity in Consanguineous Families to Efficiently Identify Candidate Genes: Application to Woodhouse-Sakati Syndrome
- Experimental protocol designed to employ Nd:YAG laser surgery for anterior chamber glaucoma detection via UBM
- Síndrome dos cabelos anágenos frouxos associada à distrofia macular: descrição de uma família
- Long-Term Intravital Imaging of the Cornea, Skin, and Hair Follicle by Multiphoton Microscope
- A Case of IFAP Syndrome with Severe Atopic Dermatitis