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Research 61–90 of 152
- Follikelhormone
- Skin manifestations of chronic kidney disease
- An unusual case report of rapunzel syndrome trichobezoar in a 3-year-old boy
- Beta thalassemia revealing hypothyroidism: A case report
- Cutaneous Ultrastructural Features of the Flaky Skin (<i>fsn</i>) Mouse Mutation
- Telogen effluvium x female pattern hair loss: is there correlation?
- Gastrointestinal bezoars: two distinct cases illustrating diagnostic and surgical challenges
- DERMATOPHYTOSIS CAUSED BY TRICHOPHYTON SPP. IN A LOCAL KITTEN
- Toxic and Metabolic Disorders of the Nervous System
- GENERALIZED DERMATITIS IN A MIXED-BREED GERMAN SPITZ DOG
- Serum drug level-related sodium valproate-induced hair loss
- Baricitinib in pediatric chronic immune thrombocytopenia and associated autoimmune conditions: a case report
- Full‐house nephropathy in antinuclear antibody‐negative systemic lupus erythematosus: A case report
- Systemic-Onset Juvenile Idiopathic Arthritis with unusual Cutaneous Manifestation and peripheral eosinophilia: Case Report
- Iron Deficiency-Induced Hair Loss Is Associated with ROS-Mediated Disruption of Wnt/β-Catenin Signaling
- Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis
- Development of a Predictive Model for Iron Levels in Bovine Muscle Tissue Using Hair as a Predictor
- Enteropathica Acrodermatitis Complicated by Necrotising Fasciitis in an Infant Admitted to the Paediatric Emergency Department of the Gabriel Touré University Hospital
- Eco-innovation in action: valorizing vegetable waste into high-value ingredients for sustainable applications
- Unilateral branch retinal artery occlusion in a patient with systemic lupus erythematosus
- Systemic Tofacitinib in Alopecia Areata: A Single Center Retrospective Descriptive Cohort Study
- A rare manifestation of STING-associated vasculopathy with onset in infancy: a case report
- Safety First: A Comprehensive Review of Nutritional Supplements for Hair Loss in Breast Cancer Patients
- The acyl-CoA binding protein is required for normal epidermal barrier function in mice
- Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma
- A.S.P.E.N. Parenteral Nutrition Trace Element Product Shortage Considerations
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Mineral Deficiencies: A Root Cause for Reduced Longevity in Mammals
- Vitiligo and Its Mimics in Childhood: A Diagnostic Framework for Hypopigmented Disorders
- The Bio-Safety Concerns of Three Domestic Temporary Hair Dye Molecules: Fuchsin Basic, Victoria Blue B and Basic Red 2