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Research 721–750 of 1000+
- Eating Disorders: Progress and Challenges
- The androgen receptor gene polyglycine repeat polymorphism is associated with memory performance in healthy Chinese individuals
- Gonadal Sex Steroids: Production, Action and Interactions in Mammals
- Lactium: A Novel Drug for Psychocutaneous Skin Disorders
- Eating disorders
- Psychosocial aspects of androgenetic alopecia
- Genetic prediction of male pattern baldness
- Body composition changes and inhibition of fat development in vivo implicates androgen in regulation of stem cell lineage allocation
- Modeling Oxidative Stress-Linked Telogen Effluvium Using Monte Carlo Simulation of Published Trichoscopy Norms and Cannabis Exposure Distributions
- 2-Substituted 4-(Thio)chromenone 6-<i>O</i>-Sulfamates: Potent Inhibitors of Human Steroid Sulfatase
- Finasteride Blocks the Reduction in Ictal Activity Produced by Exogenous Estrous Cyclicity
- Emotion Dysregulation of Women with Premenstrual Syndrome
- Kin‐cohort analysis of <i>LRRK2</i>‐G2019S penetrance in Parkinson's disease
- A preliminary study of finasteride in Tourette syndrome
- Several biological benefits of the low color temperature light-emitting diodes based normal indoor lighting source
- Psychodermatology
- Desferrioxamine treatment of aceruloplasminemia: Long‐term follow‐up
- Psychocutaneous disease
- Sexuality in premature ovarian insufficiency
- Neuropsychological Assessment in Elderly Men with Benign Prostatic Hyperplasia Treated with Dutasteride
- The Enigma of the Stigma of Hair Loss: Why is Cancer-Treatment Related Alopecia so Traumatic for Women?
- Comparison of Complications after Coronavirus Disease and Seasonal Influenza, South Korea
- Pathological findings in a case of stiff person syndrome with anti‐GAD antibodies
- Hair Tourniquet Syndrome of the Toe: Report of 2 New Cases
- Analysis of changes in microRNA expression profiles in response to the troxerutin-mediated antioxidant effect in human dermal papilla cells
- Novel <i>ABCD1</i> Gene Mutation in Adrenomyeloneuropathy with Hypoplasia and Agenesis of the Corpus Callosum
- Acquired constriction ring syndrome as a cause of inconsolable cry in a child: a case report
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- Multimodal imaging of hair follicle bulge-derived stem cells in a mouse model of traumatic brain injury
- ‘Post-finasteride syndrome’: what to tell our female patients?