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Original Articles

Coping styles in families with haemophilia

Pages 3-12 | Published online: 19 Aug 2010

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Katharine Wickel Didericksen, Amelia Muse & Rola Aamar. (2019) Rethinking Parental Coping with Child Health: A Proposed Theoretical Model. Marriage & Family Review 55:5, pages 423-446.
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Natalia Sira, Priti P. Desai, Kathryn J. Sullivan & David W. Hannon. (2014) Coping Strategies in Mothers of Children with Heart Defects: A Closer Look Into Spirituality and Internet Utilization. Journal of Social Service Research 40:5, pages 606-622.
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DavidT. Dahlbeck & Owen Richard Lightsey$suffix/text()$suffix/text(). (2008) Generalized Self-Efficacy, Coping, and Self-Esteem as Predictors of Psychological Adjustment Among Children With Disabilities or Chronic Illnesses. Children's Health Care 37:4, pages 293-315.
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Articles from other publishers (14)

Anthe Foubert, Nathalie Roussel, Valérie‐Anne Chantrain, Cédric Hermans, Catherine Lambert, Sébastien Lobet & Mira Meeus. (2022) Pain coping behaviour strategies in people with haemophilia: A systematic literature review. Haemophilia 28:6, pages 902-916.
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Ana Torres‐Ortuño, Rubén Cuesta‐Barriuso, Joaquín Nieto‐Munuera, Pilar Galindo‐Piñana & José Antonio López‐Pina. (2019) Coping strategies in young and adult haemophilia patients: A tool for the adaptation to the disease. Haemophilia 25:3, pages 392-397.
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Priti P. Desai, Abigail Torres Rivera & Emily M. Backes. (2016) Latino Caregiver Coping With Children's Chronic Health Conditions: An Integrative Literature Review. Journal of Pediatric Health Care 30:2, pages 108-120.
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R. Cuesta-Barriuso, A. Torres-Ortuño, M. López-García & J. Nieto-Munuera. (2014) Effectiveness of an educational intervention of Physiotherapy in parents of children with haemophilia. Haemophilia 20:6, pages 866-872.
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M. Binnema, L. H. Schrijvers, R. Bos, M. J. Schuurmans & K. Fischer. (2014) Coping in adult patients with severe haemophilia. Haemophilia 20:4, pages 513-518.
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Maria Ojala. (2013) Coping with Climate Change among Adolescents: Implications for Subjective Well-Being and Environmental Engagement. Sustainability 5:5, pages 2191-2209.
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S. V. Mackensen & A Gringeri. 2010. Handbook of Disease Burdens and Quality of Life Measures. Handbook of Disease Burdens and Quality of Life Measures 1895 1920 .
N. Pereda, M. Forns, T. Kirchner & D. Muñoz. (2009) Use of the Kidcope to identify socio-economically diverse Spanish school-age children's stressors and coping strategies. Child: Care, Health and Development 35:6, pages 841-850.
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S. WIEDEBUSCH, H. POLLMANN, B. SIEGMUND & F. A. MUTHNY. (2008) Quality of life, psychosocial strains and coping in parents of children with haemophilia. Haemophilia 14:5, pages 1014-1022.
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K. BEETON, D. NEAL, T. WATSON & C. A. LEE. (2007) Parents of children with haemophilia ? a transforming experience. Haemophilia 13:5, pages 570-579.
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A. M. BOTTOS, E. ZANON, M. T. SARTORI & A. GIROLAMI. (2007) Psychological aspects and coping styles of parents with Haemophilic child undergoing a programme of counselling and psychological support. Haemophilia 13:3, pages 305-310.
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Diletta Fiandaca, Paolo Bucciarelli, Ida Martinelli, Francesca Tantardini, Carmen Clemente & Pier Mannuccio Mannucci. (2006) Psychological impact of thrombosis in the young. Internal and Emergency Medicine 1:2, pages 119-126.
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H. Marijke Van Den Berg & Kathelijn Fischer. 2005. Textbook of Hemophilia. Textbook of Hemophilia 39 45 .
M. Canclini, N. Saviolo-Negrin, E. Zanon, R. Bertoletti, A. Girolami & A. Pagnan. (2003) Psychological aspects and coping in haemophilic patients: a case-control study. Haemophilia 9:5, pages 619-624.
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