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Research 331–360 of 1000+
- SELF-CARE OF MALE PATTERN HAIR LOSS – Selfcare Journal
- Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy
- Rabson-Mendenhall syndrome: two case reports and a brief review of the literature
- Surgical approach of ectropion in lamellar ichthyosis
- Ischemic onycholysis of the hands
- Dermoscopic findings in female androgenetic alopecia
- Efektivitas Terapi Minoksidil pada Alopesia Androgenetik: Studi in Vivo
- Do you know this syndrome? * Você conhece esta síndrome? *
- New drugs under investigation for the treatment of alopecias
- Un asentamiento de la primera Edad del Hierro en el término de Raposal (Arnedo, La Rioja)
- Applications and Risks of Nanomaterials Used in Regenerative Medicine, Delivery Systems, Theranostics, and Therapy
- Advances in Tissue Bioengineering and Regenerative Aesthetic Medicine: Emerging Strategies for Tissue Restoration, Functional Recovery, and Personalized Healthcare
- Acne-associated syndromes: models for better understanding of acne pathogenesis
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- Roles of tumor suppressors in regulating tumor-associated inflammation
- <i>WNT10A</i> , dermatology and dentistry
- Skin manifestations among<i>GATA2</i>-deficient patients
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Yellow and orange in cutaneous lesions: clinical and dermoscopic data
- Hair and Nail Relationship
- Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain
- An updated review of the sebaceous gland and its role in health and diseases Part 2: Pathophysiological clinical disorders of sebaceous glands
- Disease causing homozygous variants in the human hairless gene
- Ichthyosis in Unani Medicine: A Comprehensive Review of Disorders of Cornification and their Modern Dermatological Correlates
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- Oral Presentations
- 9. Immunology and Genetics
- Polycystic Ovary Syndrome, Insulin Resistance, and Obesity: Navigating the Pathophysiologic Labyrinth
- Deletion of Deoxyribonucleic Acid Binding Domain of the Vitamin D Receptor Abrogates Genomic and Nongenomic Functions of Vitamin D
- p53‐dependent transcriptional regulation of EDA2R and its involvement in chemotherapy‐induced hair loss