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Research 301–330 of 1000+
- Pattern of dyslipidemia among adult women with polycystic ovary syndrome in Port Harcourt, Nigeria
- Disorders of the skin appendages
- Hair Loss in a Female Distance Runner
- Cycle pilaire et alopécie X chez le chien
- Alopecia associated with syringomas
- Aldesleukin
- The role of vitamin D receptor mutations in the development of alopecia
- The molecular pathogenesis of Trichilemmal carcinoma
- Overview of Alopecia Areata
- Vitamins and Alopecia
- Steroidogenic Factor-1 Lineage Origin of Skin Lesions in Carney Complex Syndrome
- Bilateral Periorbital Erythema and Swelling as an Initial Presentation of Systemic Lupus Erythematosus: A Rare Case
- Systemic subchronic toxicity and comparison of four selenium nutritional supplements by 90-day oral exposure in Sprague-Dawley rats
- Bioinformatic network analysis on the molecular interactions between Parkinson’s disease, alpha-synuclein, and infertility condition
- Type 1 Diabetes Mellitus and Autoimmune Diseases: A Critical Review of the Association and the Application of Personalized Medicine
- Male gonadal function in coeliac disease: 2. Sex hormones.
- Unusual Presentation of Denys-Drash Syndrome in a Girl with Undisclosed Consumption of Biotin
- 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
- 5155 Benign Paroxysmal Positional Vertigo as a Potential Manifestation of Hypothyroidism, a Case Report
- Side effects of vitamins, amino acids, nutrition, and complementary and alternative medicine
- Prevalence of Polycystic Ovarian Syndrome in Young Adult Unmarried Females Attending Zagazig University Hospital Outpatient Clinic
- Severe Hyperandrogenism in A Premenopausal Woman With An Imaging-Negative Leydig Cell Tumor
- Alopecia Areata in the Elderly: A 10-Year Retrospective Study
- 31-Year-Old Woman With Alopecia
- This Month in the Journal
- Genetic Basis of Alopecia Areata
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene
- Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome
- Treatment of Alopecia in Children