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Berit Widerøe Njølstad, Anne Marit Mengshoel & Unni Sveen. (2019) ‘It’s like being a slave to your own body in a way’: a qualitative study of adolescents with chronic fatigue syndrome. Scandinavian Journal of Occupational Therapy 26:7, pages 505-514.
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Hedda Eik Grape, Kari Nyheim Solbrække, Marit Kirkevold & Anne Marit Mengshoel. (2017) Tiredness and fatigue during processes of illness and recovery: A qualitative study of women recovered from fibromyalgia syndrome. Physiotherapy Theory and Practice 33:1, pages 31-40.
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Articles from other publishers (20)
Meeri Keurulainen, Juha Holma, Elina Wallenius, Mikko Pänkäläinen, Jukka Hintikka & Markku Partinen. (2023) ‘I became more aware of my actions’—A qualitative longitudinal study of a health psychological group intervention for patients with myalgic encephalomyelitis/chronic fatigue syndrome. Health Expectations 26:6, pages 2312-2324.
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Janet Njelesani, Vongai Mlambo, Tsedenia Denekew & Jean Hunleth. (2022) Inclusion of children with disabilities in qualitative health research: A scoping review. PLOS ONE 17:9, pages e0273784.
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Daniel Maroti & Robert Johansson. (2021) Is Cognitive Change Necessary to Alleviate Symptoms in Patients With Functional Somatic Syndrome?. Frontiers in Psychiatry 12.
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Nikki Ow, Adriana Appau, Mohamad Matout & Nancy E. Mayo. (2021) What is QOL in children and adolescents with physical disabilities? A thematic synthesis of pediatric QOL literature. Quality of Life Research 30:5, pages 1233-1248.
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M. E. Loades, S. Vitoratou, K. A. Rimes, S. Ali & T. Chalder. (2019) Psychometric properties of the Cognitive and Behavioural Responses Questionnaire (CBRQ) in adolescents with chronic fatigue syndrome. Behavioural and Cognitive Psychotherapy 48:2, pages 160-171.
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Lauren Stephanie Jones, Emma Anderson, Maria Loades, Rebecca Barnes & Esther Crawley. (2020) Can linguistic analysis be used to identify whether adolescents with a chronic illness are depressed?. Clinical Psychology & Psychotherapy 27:2, pages 179-192.
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Silje Vagli Østbye, Maria Fredriksen Kvamme, Catharina Elisabeth Arfwedson Wang, Hanne Haavind, Trond Waage & Mette Bech Risør. (2018) ‘Not a film about my slackness’: Making sense of medically unexplained illness in youth using collaborative visual methods. Health: An Interdisciplinary Journal for the Social Study of Health, Illness and Medicine 24:1, pages 38-58.
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Hadeel A. Al‐Rawaf, Ahmad H. Alghadir & Sami A. Gabr. (2019) MicroRNAs as Biomarkers of Pain Intensity in Patients With Chronic Fatigue Syndrome. Pain Practice 19:8, pages 848-860.
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Maria Elizabeth Loades, Katharine Rimes, Kate Lievesley, Sheila Ali & Trudie Chalder. (2019) Cognitive and behavioural responses to symptoms in adolescents with chronic fatigue syndrome: A case-control study nested within a cohort. Clinical Child Psychology and Psychiatry 24:3, pages 564-579.
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Katrin Hulme, Paul Little, Abigail Burrows, Anna Julia & Rona Moss‐Morris. (2019) Subacute fatigue in primary care – two sides of the story. British Journal of Health Psychology 24:2, pages 419-442.
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Maria F. Kvamme, Catharina E. A. Wang, Trond Waage & Mette B. Risør. (2019) Careful expressions of social aspects: How local professionals in high school settings, municipal services, and general practice communicate care to youth presenting persistent bodily complaints. Health & Social Care in the Community.
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Roxanne M Parslow, Nina Anderson, Danielle Byrne, Alison Shaw, Kirstie L Haywood & Esther Crawley. (2018) Adolescent’s descriptions of fatigue, fluctuation and payback in chronic fatigue syndrome/myalgic encephalopathy (CFS/ME): interviews with adolescents and parents. BMJ Paediatrics Open 2:1, pages e000281.
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Maria E. Loades, Katharine A. Rimes, Kate Lievesley, Sheila Ali & Trudie Chalder. (2018) Illness beliefs of adolescents with CFS and their parents: the perceived causes of illness and beliefs about recovery. International Journal of Adolescent Medicine and Health 32:4.
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Amberly Brigden, Julie Barnett, Roxanne Morin Parslow, Lucy Beasant & Esther Crawley. (2018) Using the internet to cope with chronic fatigue syndrome/myalgic encephalomyelitis in adolescence: a qualitative study. BMJ Paediatrics Open 2:1, pages e000299.
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Linn Rødevand. (2017) Hvordan er det å være ungdom og leve med kronisk utmattelsessyndrom/myalgisk encefalopati? En narrativ oversikt [How is it to be an adolescent living with chronic fatigue syndrome/myalgic encephalomyelitis? A narrative review]. Scandinavian Psychologist 4.
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Hilde Nordahl Karterud, Ole Rikard Haavet & Mette Bech Risør. (2016) Social participation in young people with nonepileptic seizures (NES): A qualitative study of managing legitimacy in everyday life. Epilepsy & Behavior 57, pages 23-28.
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Denise Hinton & Susan Kirk. (2016) Families' and healthcare professionals' perceptions of healthcare services for children and young people with medically unexplained symptoms: a narrative review of the literature. Health & Social Care in the Community 24:1, pages 12-26.
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Anette Winger, Mirjam Ekstedt, Vegard B Wyller & Sølvi Helseth. (2014) ‘Sometimes it feels as if the world goes on without me’: adolescents' experiences of living with chronic fatigue syndrome. Journal of Clinical Nursing 23:17-18, pages 2649-2657.
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Kate Lievesley, Katharine A. Rimes & Trudie Chalder. (2014) A review of the predisposing, precipitating and perpetuating factors in Chronic Fatigue Syndrome in children and adolescents. Clinical Psychology Review 34:3, pages 233-248.
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Stefan Kempke, Patrick Luyten, Stephan Claes, Peter Van Wambeke, Patrick Bekaert, Lutgarde Goossens & Boudewijn Van Houdenhove. (2013) The prevalence and impact of early childhood trauma in Chronic Fatigue Syndrome. Journal of Psychiatric Research 47:5, pages 664-669.
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