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Research 241–270 of 1000+
- Differential Diagnosis of Male and Female Pattern Hair Loss
- Negative Impact of Testosterone Deficiency and 5α-Reductase Inhibitors Therapy on Metabolic and Sexual Function in Men
- Hyperaldosteronism and Hyperprogesteronism in a Cat
- Genetic Hair Disorders: A Review
- Worldwide cohort study of 46, XY differences/disorders of sex development genetic diagnoses: geographic and ethnic differences in variants
- Retinoic acid exerts sexually dimorphic effects on muscle energy metabolism and function
- Zebrafish Model of Hereditary Pigmentary Disorders
- Drug History and SLE Laboratory Findings Among Iraqi Patients: A Hospital‐Based Study
- Exploring links between acne and metabolic syndrome: a narrative review
- Effects of Melatonin Supplementation on Hormonal, Inflammatory, Genetic, and Oxidative Stress Parameters in Women With Polycystic Ovary Syndrome
- Myeloma, Paraproteinemias, and the Skin
- 9-cis-Retinoic Acid Capsules in the Treatment of AIDS-Related Kaposi Sarcoma
- Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13
- Intracranial hypertension as the first manifestation of systemic lupus erythematosus: A case report
- Translational perspectives in HTRA1-associated disorders: biomarkers, gene therapy, and future directions
- Interventions for central serous chorioretinopathy: a network meta-analysis
- Pathology of Mouse Models of Accelerated Aging
- Advancements and challenges in stem cell transplantation for regenerative medicine
- Endogenous retinoids in the hair follicle and sebaceous gland
- Novel Mutation in Sjögren-Larsson Syndrome Is Associated With Divergent Neurologic Phenotypes
- Current Therapeutic Approaches to Chronic Central Serous Chorioretinopathy
- Hair shaft disorders in children – An update
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Clinical Features and Treatment Options of Vogt-Koyanagi-Harada Disease
- Vogt-Koyanagi-Harada Disease with Oral Manifestations: A Rare Case Report
- Alopecia Areata: Understanding the Pathophysiology and Advancements in Treatment Modalities
- [Translated article] Keys to the Diagnosis of Hair Shaft Disorders: Part II
- Sebaceous Gland Atrophy in Psoriasis: An Explanation for Psoriatic Alopecia?
- Noggin overexpression inhibits eyelid opening by altering epidermal apoptosis and differentiation