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Research 301–330 of 1000+
- Deciphering the Complex Immunopathogenesis of Alopecia Areata
- National consensus on the management of patients with hyperandrogenism (2016)
- Growth hormone deficiency with late-onset hypothalamic hypoadrenocorticism associated with respiratory and renal dysfunction: a case report
- Optical Coherence Tomography Angiography Findings in Polycystic Ovary Syndrome
- Klinisch redeneren: diagnostiek bij thyreotoxicose in de eerste lijn: een case-report
- A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene
- Diagnosis and treatment of female alopecia: Focusing on the iron deficiency-related alopecia
- Hair fragility (trichorrhexis nodosa) in alopecic Pomeranian dogs
- Endogenous retinoids in the hair follicle and sebaceous gland
- Prolactin: A Mammalian Stress Hormone and Its Role in Cutaneous Pathophysiology
- Oral contraceptive pill (OCP) treatment alters the gene expression of intercellular adhesion molecule-1 (ICAM-1), tumor necrosis factor-α (TNF-α), monocyte chemoattractant protein-1 (MCP-1) and plasminogen activator inhibitor-1 (PAI-1) in polycystic ovary syndrome (PCOS) women compared to drug-naive PCOS women
- The adverse effects of commonly used medications on male fertility: a comprehensive review
- A young male with kidney damage from genetic mitochondrial disease: case report and literature review
- The role of vitamin D receptor mutations in the development of alopecia
- The epidermis: rising to the surface
- Systemic subchronic toxicity and comparison of four selenium nutritional supplements by 90-day oral exposure in Sprague-Dawley rats
- COMMENTS ON THE LETTER ON HYPONATREMIA ASSOCIATED WITH DIURETIC USE AND URINARY RETENTION IN AN OLDER MAN
- The Roles of EDA2R in Ageing and Disease
- Bioinformatic network analysis on the molecular interactions between Parkinson’s disease, alpha-synuclein, and infertility condition
- Unraveling a Rare Case: Diarrhea, Alopecia, and Polyposis
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- FOXN1 deficient nude severe combined immunodeficiency
- Steroidogenic Factor-1 Lineage Origin of Skin Lesions in Carney Complex Syndrome
- Type 1 Diabetes Mellitus and Autoimmune Diseases: A Critical Review of the Association and the Application of Personalized Medicine
- Unusual Presentation of Denys-Drash Syndrome in a Girl with Undisclosed Consumption of Biotin
- Selenium in the supplement as the probable cause of hair loss and nail dystrophy
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene
- COVID-19 and hypopituitarism
- A Kaleidoscope of Keratin Gene Expression and the Mosaic of Its Regulatory Mechanisms