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Research 391–420 of 1000+
- CUTANEOUS MASTOCYTOSIS IN CHILDREN: AN INDIAN EXPERIENCE
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- Cutaneous and Mucosal Manifestations Associated with Celiac Disease
- Systemic causes of hair loss
- Afamin serum concentrations are associated with insulin resistance and metabolic syndrome in polycystic ovary syndrome
- Use of Insulin-Sensitizing Agents in Patients With Polycystic Ovary Syndrome
- Hormonal and Surgical Treatment Options for Transgender Men (Female-to-Male)
- Female pattern hair loss
- Nanostructured Lipid Carrier for Topical Application of N-Acetyl Glucosamine
- Vitamin D receptor-mediated control of Soggy, Wise, and Hairless gene expression in keratinocytes
- Interventional studies for polycystic ovarian syndrome in children and adolescents
- Androgens in Women – Critical Evaluation of the Methods for Their Determination in Diagnostics of Endocrine Disorders
- Hirsutism – From Diagnosis to Use of Antiandrogens
- Polycystic ovary syndrome
- Dissociated skin cells regenerate hair follicles in a microwound, “The Punch Assay”
- PCOS and Obesity: Contraception Challenges
- Retinol-binding protein 4, leptin, and insulin resistance in idiopathic hirsutism and hirsute women with polycystic ovary syndrome
- The Polycystic Ovary Syndrome - Challenges and Opportunities in Adolescent Medicine
- A Comprehensive Review of Management of Patients with Infertility having Polycystic Ovarian Syndrome
- Polycystic ovary syndrome: An update on diagnosis and management
- Hairline Correction in Women Using Thinning and Micro-Graduation Techniques
- Subject Index
- Cutaneous Lupus Erythematosus
- Inositol versus Metformin administration in polycystic ovary syndrome patients
- Normal Hair Growth in Children
- Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation
- Disease causing homozygous variants in the human hairless gene
- Functional mapping of the mouse <i>hairless</i> gene promoter region
- Erasing the methyl mark: histone demethylases at the center of cellular differentiation and disease
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype