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This article discusses identifying and preventing iron deficiency anemia but provides no new clinical findings.

This study found that communication about aging across seven domains may predict successful aging in Indonesia through both positive and negative effects and efficacy toward aging.

This article reviews the characteristics of alopecia areata, highlights the psychological factors involved, and discusses South American contributions to understanding the disease, but reports no new clinical results.

This report describes a case of a 75-year-old woman whose diagnosis of hypopituitarism led to significant weight gain and improved physical function with treatment, highlighting the potential for overcoming frailty when investigating underlying causes in elderly patients.

This study concluded that placebo effects observed in older alopecia minoxidil studies are likely due to subjective hair count assessments and study design, rather than true improvements in hair growth.

This study found that serlopitant may reduce pruritus intensity compared to placebo in patients with chronic pruritus of unknown origin, though evidence is of low certainty and effects on other outcomes are unclear.

This thesis reviews the psychological and social challenges faced by men and women with androgenetic alopecia who seek treatment, but reports no new results.

This personal narrative details an individual's experience with alopecia areata, highlighting the emotional and social challenges of the condition, the impact of treatments, and the journey to regain confidence and freedom through hair regrowth with JAK inhibitors.

This study found that hair follicle stem cells in the hairpoor mouse, a model for Marie-Unna hypotrichosis, lose their quiescent state, leading to a disordered hair cycle and contributing to alopecia.

This abstract is a narrative piece discussing themes of womanhood, beauty, and resilience, and does not report any new research findings.

In this study, a mixed-methods survey of 357 balding men revealed that baldness is structurally stigmatized, with many participants experiencing distress and using treatments to combat it; others resisted stigma and expressed minimal distress.

This study found that living with Alopecia Areata patients is associated with a poorer quality of life, increased anxiety and depression, and reduced sexual satisfaction among cohabitants.

This study found that decreased pressure sensitivity and 2-point discrimination at the scalp's vertex were significantly associated with androgenetic alopecia in men.

This study found that the Alopecia Areata Symptom Impact Scale (AASIS) is a better tool than the Alopecia Areata Quality of Life Index (AA-QLI) for assessing patient-reported outcomes in alopecia areata.

This study found that individuals with alopecia areata experience variations in cortisol and insulin levels and adaptive mechanism pressures, which may serve as potential therapeutic targets.

This study reported that a large proportion of US adults with physician-diagnosed alopecia areata experience substantial emotional and mental health comorbidities and report significant stigma across all disease severities, yet few are receiving counseling or therapeutic intervention.

This narrative review explores the failure of fludalanine as an orally active antibiotic and highlights valuable insights into problem-solving strategies in drug discovery, without reporting new clinical results.

This text provides no research findings; it is a website's navigation and policy information for JAMA publications.

This study reports that patients with androgenetic alopecia had lower quality of life scores across all measured domains compared to controls, with disease severity worsening the impact, particularly socially for those under 30.

This study reported that the AAPPO tool effectively distinguishes between patients with alopecia areata based on scalp hair loss severity, whereas the EQ‐5D‐5L may underestimate the specific disease burden, particularly in psychological and social aspects.

This article provides no new data as it is a letter to the editor and lacks an abstract, focusing instead on discussing aspects of hair loss in the elderly without presenting research results.

This research emphasizes the importance of understanding patient experiences related to hair loss, highlighting that race, ethnicity, culture, resources, and mental health greatly affect these experiences. Effective counseling involves clear communication, validation, and shared decision-making to provide appropriate treatment, support, or camouflage options.

This study found that patients with alopecia areata experience significantly poorer quality of life compared to the general population, affecting mental health, social functioning, and overall health outcomes.

In this study, researchers reviewed the roles of autophagy and mitophagy in hair follicle cycles, exploring their potential links to hair loss and investigating how manipulating these pathways might offer new therapeutic strategies.

This article discusses recent, irreversible changes in the interaction between hair restoration surgeons and their patients, with no new research findings reported.

This abstract provides background information on alopecia areata, describing it as an autoimmune condition leading to non-scarring, patchy hair loss but does not report specific study results.

This study found that the Alopecia Areata Patient Priority Outcomes questionnaire is a reliable and valid tool for measuring the severity and impact of hair loss in individuals with alopecia areata.

This article reviews trichotillomania, highlighting its prevalence, common treatment options, and challenges such as secrecy and delayed treatment, but reports no new clinical results.