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Research 61–90 of 1000+
- The role of zinc in skin physiology – relevance for the pathogenesis and treatment of vitiligo
- MANIFESTATION OF ZINC DEFICIT IN KARACHI PAKISTAN; A CROSS SECTIONAL STUDY
- Zinc in Animal nutrition
- Failure of Fresh Plasma in Leiner Disease
- Exotic pediculosis and hair-loss syndrome in deer (<i>Odocoileus hemionus</i>) populations in California
- Exploring the Link Between Selenium from Wheat and Hair Loss
- Zinc in the Soil and Its Importance for the Plants and Human Health. An integrated review
- Westwood Carolina Conference on Clinical Dermatology
- Insertional mutation of the hairless locus on mouse Chromosome 14
- Telogen effluvium: Long term Covid-19 symptom
- Human Eccrine Sweat Gland Cells Can Reconstitute a Stratified Epidermis
- Early skin biopsy is helpful for the diagnosis and management of neonatal and infantile erythrodermas
- The Pathogenesis of Primary Cicatricial Alopecias
- Alopecia Areata and Season of Onset: A Retrospective Study of 492 Cases
- Increased risk of alopecia areata in patients with autism spectrum disorders: A Korean nationwide population-based study
- Feeding the skin: The emerging role of nutritional intervention in dermatological disorders
- 477 Dietary fat- and obesity-sensitive dermal adipocyte PKCβ induction and inflammation cross-talk
- Skin Cancer: Mechanisms and Human Relevance
- Alopecia areata − animal models
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- The Role of Sebaceous Gland Activity and Scalp Microfloral Metabolism in the Etiology of Seborrheic Dermatitis and Dandruff
- A rare manifestation of STING-associated vasculopathy with onset in infancy: a case report
- Professor Han Shirong's Dialectical Analysis of the Experience of Treating Spot Baldness
- Understanding Alopecia Areata: An Integrative Review of Causes, Mechanisms, and Management Strategies
- Demodex cati and feline immunodeficiency virus co-infection in a cat
- First Case of Degenerative Mucinotic Mural Folliculitis in Brazil
- Skin Manifestations in Primary Immunodeficient Children
- Atrichia With Papular Lesions
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Alymphoid cystic thymic dysgenesis - FOXN1 gene mutation: a rare case report of two siblings