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Research 961–990 of 1000+
- Repurposing Finasteride and Serotonin Reuptake Inhibitors as Novel Antimicrobials: A Dual-Action Approach to Target Bacterial and Fungal Pathogens
- The self in the obsessive–compulsive-related disorders: hoarding disorder, body dysmorphic disorder, and trichotillomania
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- Silver Nanoparticles Derived from <i>Artocarpus heterophyllus</i> for Antimicrobial Nano-gels:A Green Synthesis Approach
- Erosive Pustular Dermatosis of the Scalp: A Clinicopathologic Study of Fifty Cases
- Bioguided Fraction and Isolation of the Antitumor Components from<i>Phyllanthus niruri</i>L.
- 13C-NMR study of 4-azasteroids in solution and solid state
- Design, Synthesis and Evaluation of N13-Substituted Evodiamine Derivatives against Human Cancer Cell Lines
- Oligomenorrhoea in Exercising Women
- Canine cutaneous epitheliotropic T-cell lymphoma with vesiculobullous lesions resembling human bullous mycosis fungoides
- P378: Expanding the phenotype of hyper-IgE syndrome: Heterozygous VUS in IL6ST with elevated serum IgE and isolated abscesses
- TRANSTORNOS DISSOCIATIVOS EM PACIENTES VÍTIMAS DE ABUSO SEXUAL NA INFÂNCIA
- Trend and Co-occurrence Network of COVID-19 Symptoms From Large-Scale Social Media Data: Infoveillance Study (Preprint)
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- An X-Linked Gene Involved in Androgenetic Alopecia: A Lesson to Be Learned from Adrenoleukodystrophy
- Novel <i>KRT83</i> and <i>KRT86</i> mutations associated with monilethrix
- Pharmacological regulation of tissue fibrosis by targeting the mechanical contraction of myofibroblasts
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- Trichothiodystrophy Associated with Urologic Malformation and Primary Hypercalduria
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Rapidly progressive diffuse fibrosing alopecia
- Atypical pediatric presentation of alopecic and aseptic nodules of the scalp with features of dissecting cellulitis
- Novel small‐insertion mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Case Report: Triple autoimmune overlap: rheumatoid arthritis, systemic lupus erythematosus, and hypereosinophilic asthma with systemic manifestations
- Vogt-Koyanagi-Harada Disease with Oral Manifestations: A Rare Case Report
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant
- Management of Alopecia and Onychomycosis in a Lupus Patient
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- A case of <i>MBTPS1</i>‐related disorder due to compound heterozygous variants in <i>MBTPS1</i> gene: Genotype–phenotype expansion and the emergence of a novel syndrome