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題名:彈性病況:失智家庭的照顧軌跡
書刊名:臺灣社會學
作者:洪晨碩
作者(外文):Hong, Chen-shuo
出版日期:2014
卷期:28
頁次:頁59-96
主題關鍵詞:失智症照顧不確定性軌跡DementiaCareUncertaintyTrajectory
原始連結:連回原系統網址new window
相關次數:
  • 被引用次數被引用次數:期刊(3) 博士論文(0) 專書(0) 專書論文(0)
  • 排除自我引用排除自我引用:3
  • 共同引用共同引用:25
  • 點閱點閱:29
期刊論文
1.林文源(20090600)。腹膜透析隱形實作與軌跡。臺灣社會學,17,1-59。new window  延伸查詢new window
2.吳嘉苓(20111200)。編排風險:多胚胎孕育的多重社會科技網絡。臺灣社會學,22,111-156。new window  延伸查詢new window
3.王文甫、王釧如、黃耀庭(2010)。心理衡鑑之外--談阿兹海默氏病患者的評估。Acta Neurologica Taiwanica,19(1),70-75。  延伸查詢new window
4.范齡勻、陳達夫、邱銘章(2012)。阿兹海默症藥物治療的現在與未來。台灣醫學,16(4),397-403。  延伸查詢new window
5.黃惠琪、黃宗正(2012)。阿兹海默症精神行爲症狀的藥物治療。台灣醫學,16(4),382-389。  延伸查詢new window
6.歐陽文貞(2011)。老人失智症的藥物治療及其重要課題。中南盟硏究年刊,4(1),49-71。  延伸查詢new window
7.鄭冠瑾、邱逸榛、李佳琳、廖順奎、李淑花(20110600)。家庭照顧者壓力感受與壓力生理指標相關性之探討。護理雜誌,58(3),43-52。new window  延伸查詢new window
8.Allen, Davina、Griffiths, Lesley、Lyne, Patricia(2004)。Understanding Complex Trajectories in Health and Social Care Provision。Sociology of Health & Illness,26(7),1008-1030。  new window
9.Beard, Renee L.(2004)。In Their Voices: Identity Preservation and Experiences of Alzheimer's Disease。Journal of Aging Studies,18(4),415-428。  new window
10.Beard, Renee L.、Fox, Patrick J.(2008)。Resisting Social Disenfranchisement: Negotiating Collective Identities and Everyday Life with Memory Loss。Social Science & Medicine,66(7),1509-1520。  new window
11.Caddell, Lisa S.、Clare, Linda(2010)。The Impact of Dementia on Self and Identity: A Systematic Review。Clinical Psychology Review,30(1),113-126。  new window
12.Chow, T. W.、Liu, C. K.、Fuh, J. L.、Leung, V. P. Y.、Tai, C. T.、Chen, Li-Wen、Cummings, J. L.(2002)。Neuropsychiatric Symptoms of Alzheimer's Disease Differ in Chinese and American Patients。International Journal of Geriatric Psychiatry,17(1),22-28。  new window
13.Dumit, Joseph(2006)。Illnesses You Have to Fight to Get: Facts as Forces in Uncertain, Emergent Illnesses。Social Science & Medicine,62(3),577-590。  new window
14.Fair, Brian(2010)。Morgellons: Contested Illness, Diagnostic Compromise and Medicalisation。Sociology of Health & Illness,32(4),597-612。  new window
15.Hayes, Jeanne、Zimmerman, Mary K.、Boylstein, Craig(2010)。Responding to Symptoms of Alzheimer's Disease: Husbands, Wives, and the Gendered Dynamics of Recognition and Disclosure。Qualitative Health Research,20(8),1101-1115。  new window
16.Barker, Kristin K.(2008)。Electronic Support Groups, Patient-Consumers, and Medicalization: The Case of Contested Illness。Journal of Health and Social Behavior,49(1),20-36。  new window
17.Broom, Dorothy H.、Woodward, Roslyn V.(1996)。Medicalisation Reconsidered: Toward a Collaborative Approach to Care。Sociology of Health & Illness,18(3),357-378。  new window
18.Bury, Michael(1982)。Chronic Illness as Biographical Disruption。Sociology of Health and Illness,4(2),167-182。  new window
19.Corbin, Juliet M.、Strauss, Anselm L.(1985)。Managing Chronic Illness at Home: Three Lines of Work。Qualitative Sociology,8(3),224-247。  new window
20.Ikels, Charlotte(1998)。The Experience of Dementia in China。Culture, Medicine and Psychiatry,22(3),257-283。  new window
21.Ikels, Charlotte(2002)。Constructing and Deconstructing the Self: Dementia in China。Journal of Cross-Cultural Gerontology,17(3),233-251。  new window
22.MacRae, Hazel(2008)。'Making the Best You Can of It' : Living with Early-Stage Alzheimer's Disease。Sociology of Health & Illness,30(3),396-412。  new window
23.MacRae, Hazel(2011)。Self and Other: The Importance of Social Interaction and Social Relationships in Shaping the Experience of Early-Stage Alzheimer's Disease。Journal of Aging Studies,25(4),445-456。  new window
24.Pearce, Alison、Clare, Linda、Pistrang, Nancy(2002)。Managing Sense of Self: Coping in the Early Stages of Alzheimer's Disease。Dementia,1,173-192。  new window
25.Timmermans, Stefan、Buchbinder, Mara(2010)。Patients-in-Waiting: Living between Sickness and Health in the Genomics Era。Journal of Health and Social Behavior,51(4),408-423。  new window
26.Timmermans, Stefan、Angell, Alison(2001)。Evidence-Based Medicine, Clinical Uncertainty, and Learning to Doctor。Journal of Health and Social Behavior,42(4),342-359。  new window
27.曾凡慈(20101200)。醫用者的運籌行動:形塑早期療育的照護軌跡。臺灣社會學刊,45,63-116。new window  延伸查詢new window
28.傅中玲(20080800)。臺灣失智症現況。臺灣老年醫學暨老年學雜誌,3(3),169-181。  延伸查詢new window
29.邱麗蓉、謝佳容、蔡欣玲(20070900)。失智症病患主要照護者的壓力源、評價和因應行為與健康之相關性探討。精神衛生護理雜誌,2(2),31-44。  延伸查詢new window
學位論文
1.洪晨碩(2013)。協商失智經驗:診斷裝配、生活秩序與身份認同(碩士論文)。國立台灣大學,台北。  延伸查詢new window
圖書
1.邱銘章、湯麗玉(2006)。失智症照護指南。臺北市:原水文化出版社。  延伸查詢new window
2.褚士瑩(2012)。忘了:走一段無悔的失智照護旅程。時報文化出版企業股份有限公司。  延伸查詢new window
3.Charmaz, Kathy(1991)。Good Days, Bad Days: The Self in Chronic Illness and Time。New Brunswick, NJ:Rutgers University Press。  new window
4.Corbin, Juliet M.、Strauss, Anselm L.(1988)。Unending Work and Care: Managing Chronic Illness at Home。Jossey-Bass Publishers。  new window
5.Strauss, Anaelm L.、Fagerhaugh, Shizuko、Suczek, Barbara、Wiener, Carolyn(1997)。Social Organization of Medical Work。New Brunswick, NJ:Transaction Publishers。  new window
6.Strauss, Anselm L.(1978)。Negotiations: Varieties, contexts, Processes, and social order。San Francisco, CA:Jossey Bass。  new window
7.Strauss, Anselm L.(1993)。Continual Permutations of Action。New York:Aldine de Gruyter。  new window
8.Goffman, Erving(1963)。Stigma: Notes on the Management of Spoiled Identity。Englewood Cliffs, New Jersey:Prentice-Hall。  new window
9.Strauss, A.(1987)。Qualitative Analysis for Social Scientist。Cambridge University Press。  new window
10.American Psychiatric Association(2000)。Diagnostic and Statistical manual of mental disorders。Washington, DC:Book Promotion & Service LTD。  new window
其他
1.黃玉芳(20100815)。失智症藥給付醫師批:耍病人。  延伸查詢new window
2.詹建富(20130801)。失智症藥健保給付今起放寬。  延伸查詢new window
圖書論文
1.劉宏彬(2008)。轉個彎欣賞他。失智症完全手册:台灣失智症協會專家智慧集結。台北市:健康文化。  延伸查詢new window
2.藍佩嘉(2012)。質性個案硏究法:紮根理論與延伸個案法。社會及行爲科學硏究法(二):質性硏究法。台北市:台灣東華。  延伸查詢new window
3.Barker, Kristin K.(2010)。The Social Construction of Illness: Medicalization and Contested Illness。Handbook of Medical Sociology。Nashville, TN:Vanderbilt University Press。  new window
4.Fielding, Stephen L.(1999)。Uncertainty--Which Diagnosis and Treatment?。The Practice of Uncertainty: Voices of Physicians and Patients in Medical Malpractice Claims。London:Auburn House。  new window
5.Lyman, Karen A.(2008)。Infantilization: The Medical Model of Care。Perspectives in Medical Sociology。Prospect Heights, IL:Waveland Press。  new window
 
 
 
 
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