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Research 91–120 of 134
- Supplementation of Amra Beej Majja Churna in Vitamin B12 Deficiency - A Case Study
- TONGUE, RED
- IRON DEFICIENCY: AN UNDER-RECOGNIZED PROBLEM IN KIDNEY TRANSPLANTATION. RISKS OF IRON TREATMENT.
- ZALCITABINE
- ESCITALOPRAM
- Mechanism of Cuticle Hole Development in Human Hair Due to UV-Radiation Exposure
- Protection and Restoration of Damaged Hair via a Polyphenol Complex by Promoting Mechanical Strength, Antistatic, and Ultraviolet Protection Properties
- Floral attractants in the black orchid Brasiliorchis schunkeana (Orchidaceae, Maxillariinae): clues for presumed sapromyophily and potential antimicrobial activity
- The Role of the Slc39a Family of Zinc Transporters in Zinc Homeostasis in Skin
- Skin manifestations associated with COVID-19
- Mucocutaneous manifestations in children with human immunodeficiency virus infection
- Prophylaxis and Management of Skin Toxicities
- Skin manifestations associated with systemic diseases – Part I
- Female pattern hair loss
- Pica for Uncooked Basmati Rice in Two Women with Iron Deficiency and a Review of Ryzophagia
- A study on efficacy of oral zinc therapy for treatment of acrodermatitis enteropathica
- The Role of Vitamin D3 Deficiency and Colonization of the Oral Mucosa by Candida Yeast-like Fungi in the Pathomechanism of Psoriasis
- Acquired Acrodermatitis Enteropathica in a 28-Year-Old Male with Type 1 Diabetes
- Skin, mucosa and nail findings in hospitalized pediatric patients with Coronavirus disease-2019 (COVID-19)
- Identification of Epigenetic Regulator‐Associated Genes in Keloid Disease Through Integrated Bulk and Single‐Cell Transcriptomics With RT ‐ qPCR Validation
- Black Hairy Tongue Syndrome: Case Report and Review of the Literature
- When Diet Trends Go Viral: Cutaneous Manifestations of Social Media-Driven Fad Diets and Supplements
- The Nutrient–Skin Connection: Diagnosing Eating Disorders Through Dermatologic Signs
- Diagnosis and treatment of female alopecia: Focusing on the iron deficiency-related alopecia
- Enteropathica Acrodermatitis Complicated by Necrotising Fasciitis in an Infant Admitted to the Paediatric Emergency Department of the Gabriel Touré University Hospital
- Case report: Acrodermatitis enteropathica result from a novel SLC39A4 gene mutation
- Recurrent pruritic polymorphic lesions associated with weight loss
- Identification of the Key Genes Associated with Different Hair Types in the Inner Mongolia Cashmere Goat
- Nanocarrier Systems for Transdermal Drug Delivery
- Evolution, classification, structure, and functional diversification of steroid 5α-reductase family in eukaryotes