Bibliografia

Principal

  • Taylor, S. E. (2012). Health Psychology (8th Edition). New York: McGraw Hill Marini, I. & Stebnicki, M. (2012). The psychological and social impact of illness and disability. 6th ed. New York: NY: Springer Publishing Company. Joyce-Moniz, L., & Barros, L. (2005). Psicologia da doença para cuidados de saúde: desenvolvimento e intervenção. Porto: Asa. :

Secundária

  • Wills, T.A. (1997). Social support and health. In A. Baum, S. Newman, J. Weinman, R. West, & C. McManus (Eds.), Cambridge handbook of psychology, health and medicine (168-170). United Kingdom: Cambrigde University Press. Taylor, S.E. & Sirois, F.M. Cox, D. N. (2012). Health Psychology (2nd Canadian ed.) McGraw-Hill-Ryerson. Straub, R. O. (2012). Health psychology: A biopsychosocial approach (3rd Ed.). N.Y: Worth. Stanton, A. L., Tracey, B., Revenson, A., & Tennen, H. (2007). Health Psychology: Psychological Adjustment to Chronic Disease. Annual Review of Psychology, 58, 565-592. Sparud - Lundin, C., Ohrn, I., & Danielson, E. (2009). Redefining relationships and identity in young adults with type 1 diabetes. Journal of Advanced Nursing, 66 (1): 128-138. doi: 10.1111/j.1365-2648.2009.05166.x Smart, J. (2012). Disability Across the Developmental Life Span. NY: Springer Publishing Company Sapolsky, R. (2004). Why Zebras Don't Get Ulcers (3rd Ed.). New York: St. Martins. Rintala, T. M., Paavilainen, E., & Astedt - Kurki, P. (2013). Everyday life of a family with diabetes as described by adults with type 1 diabetes. European Diabetes Nursing, 10 (3): 86-90. Rimé, B. (1989). Le partage social des émotions. In B. Rimé & K. Scherer (Eds.), Les émotions (pp. 271-303). Neuchâtel: Delachaux et Niestlé. Pereira S. M. (2010). Cuidados paliativos. Confrontar a Morte. Lisboa: Universidade Católica Editora, 2010. Patton, S. (2011). Adherence to diet in youth with type 1 diabetes. Journal of the American Dietetic Association, 111 (4) : 550-555. Nolan, M. Lundh, U., Grant, G., & Keady, J. (2003). Parternships in family care: Understanding the caregiving career. Maidenhead: Open University Press. Nils, F., & Rimé, B. (2010). Beyond the myth of venting: Social sharing modes determine emotional and social benefits from distress disclosure. Manuscript submitted for publication. Nelson, G., Kloos, B., & Ornelas, J. (2014). Community Psychology and Community Mental health. Towards transformative change. Oxford: Oxford University Press. Mendelsohn, G., de la Tour, F., Coudin, G., & Raveau, F. (1984). A Comparative Study of the Adaption to Breast Cancer and Its Treament in French and American Women. Cahiers d'Anthropologie et Biométrie Humaine, 2, 71-96. Marini, I., & Stebnicki, M. (2012). The psychological and social impact of illness and disability (6th ed.). New York: NY: Springer Publishing Company Lubkin, M., & Larsen, P.D. (2009). Chronic Illness Impact and Interventions (6th Ed.). Boston: Jones and Bartlett Publishers. Lloyd-Williams, M. (2003). Psychosocial Issues in Palliative Care. Oxford: Oxford University Press, 2003. Lima, M. L., Bernardes, S. F, & Marques, S. (2014). Psicologia Social da saúde: Investigação e Intervenção em Portugal (Vol.1). Lisboa: Sílabo. Letamo, G. (2011). Social and Psychological Aspects of HIV/AIDS and their Ramifications. ISBN 978-953-307-640-9, InTech. American Diabetes Association - ADA (2003). Just for teens - Living with diabetes type 1. Recuperado de http://www.diabetes.org. Luecken, L., J., & Gallo, L. C. (2008). Handbook of Physiological Research methods in Health psychology. Los Angeles: Sage Lacroix, A., Assal, J-Ph., & Cifali-Bega, M. (2013). L'éducation thérapeutique :Il fallait bien commencer... - Entretien avec Anne Lacroix et Jean-Philippe Assal. Education Permanente, 195, 11-24. Kasl-Godley. J. E., King, D. A., & Quill. T. E. (2014). Opportunities for Psychologists in Palliative Care Working With Patients and Families Across the Disease Continuum. American Psychologist, 69(4), 364-376. Joyce-Moniz, L., & Barros, L. (2005). Psicologia da doença para cuidados de saúde: desenvolvimento e intervenção. Porto: Asa. Holland, J. C., Breitbart, W. S., Jacobsen, P. B., Lederberg, M. S., Loscalzo, M. J., & McCorkle, R. S. (2010). Psycho-Oncology (2nd Ed.). New York: Oxford University Press. Griffiths, L.S., Field, B.J., Lustman, P.J. (1990). Life stress and social support in diabetes: association with glycemic control. International Journal of Psychiatry in Medicine, 20, 365-372. Fisher, E.B., Delamater, A.M., Bertelson, A.D., & Kirkley, B.G. (1982). Psychological factors in diabetes and its treatment. Journal of Consulting and Clinical Psychology, 50(6), 993-1003. England-Kennedy, E. S., & Horton, S. (2011). "Everything that I thought that they would be, they weren't": Family systems as support and impediment to recovery. Social Science & Medicine, 73, 1222-1229. Die, M., & López, E. (2000). Aspectos Psicológicos en Cuidados Paliativos. La Comunicación con el Enfermo y la Familia. Madrid:Ades Ediciones. Dell Orto, A. E., & Power, P. W. (2007). The psychological and social impact of illness and disability (5th ed). New York: NY: Springer Publishing Company. Kalus, C, Beloff, H., Brennan J et al. (2008). The Role of Psychology in End of Life Care. A report published by the Professional Practice Board of the British Psychological Society. Leicester: The British Psychological Society, 2008. Jouet, E. (2013).Faire de sa maladie un apprentissage. L'exemple du projet Emilia. Education Permanente, 195, 73-84. Delgado, A. B., & Lima, M. L. (2001). Contributo para a validação concorrente de uma medida de adesão aos tratamentos. Psicologia: Saúde e Doenças, 1, 81-100. Coudin, G., & Mollard, J. (2011). Être aidant de malade Alzheimer : difficultés, stratégies de faire face et gratifications. Ger Psychol Neuropsychiatr Vieil, 9(3): 363-789. Feuerstein, M., & Findley, P. (2006). The cancer survivor's guide: The essential handbook to life after cancer. NY: Marlowe & Co. Cordella, M., & Poiani, A. (2014). Behavioural Oncology: Psychological, Communicative, and Social Dimensions. New York: Springer. Chan, F., Cardoso, E. S., & Chronister, J. A. (2009). Understanding psychosocial adjustment to chronic illness and disability: A handbook for evidence-based practitioners in rehabilitation. NY: Springer Publishing Company. Cantisano, N., Rime, B. & Munoz-Sastre, M. (2012). The Social sharing of emotion in HIV/AIDS: A comparative study of HIV/AIDS, diabetic and cancer patients. Jornal of Health Psychology. 1-13. Bernardes, S. F. (2010). Sobre a Contextualidade dos Enviesamentos de Sexo nos Julgamentos de Dor. Lisboa: Fundação Calouste Gulbenkian/ Fundação para a Ciência e Tecnologia. Bennett, P. & Morrison, V. (2012). An introduction to health psychology (3th ed.) Harlow: Pearson. Baum, A., Revenson, T. A., & Singer, J. (2012). Handbook of health psychology (2nd ed.). NY: Psychology Press. Arranz, P., Barbero, J.J., Barreto, P., & Bayés, R. (2003). Intervención Emocional en Cuidados Paliativos. Modelo y Protocolos. Barcelona: Ariel Ciencias Médicas. Barros, L., Matos, M. G., & Batista-Foguet, J. (2008). Chronic diseases, Social context and adolescent health: Results of the Portuguese National Health Behaviour in School-Aged Children Survey. Revista Brasileira de Terapias Cognitivas,4(1), 29-34. Barros, L. (2003). Psicologia pediátrica: uma perspectiva desenvolvimentista (2ª Edição Revista e Aumentada). Lisboa: Climepsi. Arigo, D., Suls, J., & Smyth, J. M. (2014). Social comparisons and chronic illness: Literature synthesis and clinical implications. Health Psychology Review, 8, 154-214. Anderson, R. M., & Funnell, M. M. (2010). Patient empowerment: Myths and misconceptions. Patient Education and Counseling, 79(3), 277-282. :