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Research 61–90 of 1000+
- “Hair is your crown and glory” – Black women’s experiences of living with alopecia and the role of social support
- Perceived Stigma Among Adults With Alopecia Areata in the United States
- Social Perception of Male Faces. Individuals, Clusters, Dimensions
- Perceived Stress, Illness and Stigma in Patients with Alopecia Areata
- Social Hair Plucking’s Associations with Other Behaviors and Its Health Considerations, in Captive Rhesus Macaques ( <i>Macaca mulatta</i> )
- Persistent escalation of alcohol consumption by mice exposed to brief episodes of social defeat stress: suppression by CRF-R1 antagonism
- Men’s baldness stigma: A mixed methods international survey
- Psychosocial burden and the impact of illness perceptions and stigma on quality of life, anxiety and depression in alopecia areata: results from the Alopecia + Me study
- THE VICIOUS CYCLE OF POLYCYSTIC OVARY SYNDROME AND BINGE EATING DISORDER: A REVIEW OF METABOLIC, PSYCHOLOGICAL, AND IATROGENIC PATHWAYS
- “I wouldn’t wish alopecia on my worst enemy” Adolescents’ and Parents’ Experiences of Alopecia
- Neurosteroids, neuroactive steroids, and symptoms of affective disorders
- Disentangling the Coronavirus Disease 2019 Health Disparities in African Americans: Biological, Environmental, and Social Factors
- The prevalence of skin diseases in Greece, impact on quality of life and stigmatization: A population‐based survey study
- Comprehensive Evaluation of Androgenetic Alopecia: Demographic Characteristics, Psychosocial Impact, and the Role of Social Media in Treatment Choices
- Identification and characterization of alopecia areata subgroups regarding quality of life impairment based on demographic, clinical, psychological, and social factors
- Listening to patients: A qualitative study on diagnostic delay, coping strategies and stigma in early‐onset colorectal cancer
- “I am now being who I am and I’m proud of it”: Hair related personal and social identity and subjective wellbeing of older Black women in the UK
- Reconsidering the classification of vitiligo and alopecia as cosmetic concerns in Medicaid and Tricare policies
- Living with grief: a phenomenological analysis of the lived experience of PCOS
- Association between Androgenetic Alopecia and Psychosocial Disease Burden: A Cross-Sectional Survey among Polish Men
- Association between androgenetic alopecia and psychological well-being: a systematic review and meta-analysis
- Psychological Dimensions of Hair Transplantation: A Narrative Review of Current Evidence
- Androgenetic alopecia: What impact does it have on the quality of Life?
- Exploring the Lived Experiences and Coping Mechanisms of Unmarried Women with Polycystic Ovary Syndrome (PCOS) in Pakistan
- Alopecia Areata in Latin America: Where are We and Where are We Going?
- Beyond health-related quality of life: initial psychometric validation of a new scale for addressing the gap in assessing the full range of alopecia areata psychosocial burden
- Book reviews
- Mood disorders and quality of life in polycystic ovary syndrome
- Perceived Functional Impact of Abnormal Facial Appearance; Marlene Rankin, Ph.D., and Gregory L. Borah, M.D.
- A Gender Hypothesis of sex disparities in adverse drug events