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- “I wouldn’t wish alopecia on my worst enemy” Adolescents’ and Parents’ Experiences of Alopecia
- Losing Hair, Losing Points?: The Effects of Male Pattern Baldness on Social Impression Formation1
- The psychosocial impact of alopecia in men: A mixed‐methods survey study
- Factors Affecting the Psychosocial Distress of Patients with Alopecia Areata: A Nationwide Study in Korea
- Psychosocial Impact of Hirsutism in Female Patients Attending Dermatology OPD of CMH Kharian
- Male experiences of hair removal and loss: depilation practices and motivations
- Psychosocial impact of androgenetic alopecia on men: A systematic review and meta-analysis
- Psychosocial comorbidities in patients with paediatric alopecia areata: a literature review
- Quality of life and psychosocial impact of scarring and non‐scarring alopecia in women
- PERCEPÇÃO PSICOSSOCIAL DE PACIENTES COM ALOPECIA ANDROGENÉTICA FEMININA / PSYCHOSOCIAL PERCEPTION OF PATIENTS WITH FEMALE ANDROGENETIC ALOPECIA
- Patient-Reported Psychosocial Burdens and Quality of Life and Work Productivity Impacts Among Patients with Clinically Distinct Alopecia Areata Severity Profiles
- The psychosocial effect of androgenetic alopecia in males and females
- Analysing the patient experience of COVID‐19: Exploring patients' experiences of hospitalisation and their quality of life post discharge
- Alopecia in lupus: Experience from a tertiary referral centre
- Alopecia and Mental Health: Psychosocial Burden, Neuroendocrine Mechanisms, and Therapeutic Implications
- Multimodal Reconstructive Treatment of the Face and Scalp Following Catastrophic Burn Injury: An Eight-Year Experience with Structural Fat Grafting, Follicular Unit Excision Hair Transplantation, and Scalp Micropigmentation
- Long-term hair loss associated with brentuximab vedotin–containing chemotherapy and its psychosocial impact: A retrospective observational study conducted at the Royal Marsden Hospital.
- Clinical Assessment of Alopecia Areata Severity and Validating the Patient Experience: A Vodcast
- Demographics and Clinical Characteristics among Patients with Distinct Psychosocial Burden Profiles Related to Vitiligo: Results of a Latent Class Analysis
- 75392 Psychosocial Burden of Severe Pediatric Alopecia Areata and Strategies for Mitigation: A Narrative Evidence Synthesis
- The hidden burden of visibility: Social appearance anxiety in patients with alopecia areata – A comparative cross-sectional study
- Health‐related quality of life (hrQoL) among patients with primary cicatricial alopecia (PCA): A systematic review
- Gender Differences in Psychosocial Outcomes of Hair Loss Resulting from Childhood Irradiation for Tinea Capitis
- Effects of Self-Perceived Hair Loss in a Community Sample of Men
- The psychosocial impacts of vitiligo, psoriasis, and alopecia areata on pediatric patients
- Anxiety, depression, and quality of life in children and adults with alopecia areata: A systematic review and meta-analysis
- To Feel Again: The Strength of a Support Community
- The most impactful aspects of living with alopecia areata among patients commencing systemic treatments: Evaluating patients’ perspectives to guide therapy
- 44313 Self-Stigmatization and Alopecia Areata; Exploring the Role of Social Support, Helplessness, and Illness Acceptance
- Psychoemotional Outcomes of Permanent Eyebrow Correction in Patients with Alopecia and After Chemotherapy