Artykuły w czasopismach na temat „Carers”
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Mitchell, Eileen. "Managing Carer Stress: An Evaluation of a Stress Management Programme for Carers of People with Dementia". British Journal of Occupational Therapy 63, nr 4 (kwiecień 2000): 179–84. http://dx.doi.org/10.1177/030802260006300407.
Pełny tekst źródłaJulieta, Camino, Khondoker Mizanur, Kishita Naoko i Mioshi Eneida. "537 - Reported and observed task performance in dementia and the role of the carer management style". International Psychogeriatrics 33, S1 (październik 2021): 81. http://dx.doi.org/10.1017/s1041610221002325.
Pełny tekst źródłaFitzgerald, Leslie R., Michael Bauer, Susan H. Koch i Susan J. King. "Hospital discharge: recommendations for performance improvement for family carers of people with dementia". Australian Health Review 35, nr 3 (2011): 364. http://dx.doi.org/10.1071/ah09811.
Pełny tekst źródłaBerk, Lesley, i Michael Berk. "Who cares about carers?" Australian & New Zealand Journal of Psychiatry 49, nr 10 (7.09.2015): 936–37. http://dx.doi.org/10.1177/0004867415605621.
Pełny tekst źródłaPring, Tim. "Who cares for carers?" Aphasiology 13, nr 12 (grudzień 1999): 914–17. http://dx.doi.org/10.1080/026870399401687.
Pełny tekst źródłavan Haeften-van Dijk, A. Marijke, Franka J. M. Meiland, Bart J. J. Hattink, Ton J. E. M. Bakker i Rose-Marie Dröes. "Community day care with carer support versus usual nursing home-based day care: effects on needs, behavior, mood, and quality of life of people with dementia". International Psychogeriatrics 28, nr 4 (7.12.2015): 631–45. http://dx.doi.org/10.1017/s1041610215001921.
Pełny tekst źródłaMcConachy, Diana, i Karalyn McDonald. "Issues for Primary, Informal, Home-based Carers of People Living with AIDS". Australian Journal of Primary Health 5, nr 1 (1999): 30. http://dx.doi.org/10.1071/py99004.
Pełny tekst źródłaGraham, Candida R., Sube Banerjee i Randeep S. Gill. "Using postal questionnaires to identify carer depression prior to initial patient contact". Psychiatric Bulletin 33, nr 5 (maj 2009): 169–71. http://dx.doi.org/10.1192/pb.bp.108.020982.
Pełny tekst źródłaEwing, Gail, i Gunn Grande. "51 How do family carers feature in end of life care policy? scoping review and narrative summary of uk national policy/guidelines on implementing carer assessment and support". BMJ Supportive & Palliative Care 8, nr 3 (wrzesień 2018): 379.1–379. http://dx.doi.org/10.1136/bmjspcare-2018-mariecurie.51.
Pełny tekst źródłade Andrés-Jiménez, Elena, Rosa Mª Limiñana-Gras i Encarna Fernández-Ros. "Personality and Dementia: an Approach to Differential Profile of the Caregiver". European Journal of Investigation in Health, Psychology and Education 1, nr 3 (22.09.2011): 85–94. http://dx.doi.org/10.1989/ejihpe.v1i3.7.
Pełny tekst źródłade Andrés-Jiménez, Elena, Rosa Mª Limiñana-Gras i Encarna Fernández-Ros. "Personality and Dementia: an Approach to Differential Profile of the Caregiver". European Journal of Investigation in Health, Psychology and Education 1, nr 3 (22.09.2011): 85–94. http://dx.doi.org/10.3390/ejihpe1030007.
Pełny tekst źródłaMowforth, Oliver Daniel, Benjamin Marshall Davies i Mark Reinhard Kotter. "Quality of Life Among Informal Caregivers of Patients With Degenerative Cervical Myelopathy: Cross-Sectional Questionnaire Study". Interactive Journal of Medical Research 8, nr 4 (7.11.2019): e12381. http://dx.doi.org/10.2196/12381.
Pełny tekst źródłaKirtley, Jenna, John Chiocchi, Jon Cole i Mark Sampson. "Stigma, Emotion Appraisal, and the Family Environment as Predictors of Carer Burden for Relatives of Individuals Who Meet the Diagnostic Criteria for Borderline Personality Disorder". Journal of Personality Disorders 33, nr 4 (sierpień 2019): 497–514. http://dx.doi.org/10.1521/pedi_2018_32_355.
Pełny tekst źródłaBell, Lorraine, Kate Anderson, Afaf Girgis, Samar Aoun, Joan Cunningham, Claire E. Wakefield, Shaouli Shahid i in. "“We Have to Be Strong Ourselves”: Exploring the Support Needs of Informal Carers of Aboriginal and Torres Strait Islander People with Cancer". International Journal of Environmental Research and Public Health 18, nr 14 (7.07.2021): 7281. http://dx.doi.org/10.3390/ijerph18147281.
Pełny tekst źródłaPoon, A. W. C., C. Harvey, A. Mackinnon i L. Joubert. "A longitudinal population-based study of carers of people with psychosis". Epidemiology and Psychiatric Sciences 26, nr 3 (5.02.2016): 265–75. http://dx.doi.org/10.1017/s2045796015001195.
Pełny tekst źródłaDavies, Andrew, Jennifer Todd, Fiona Bailey, Amanda Gregory i Melanie Waghorn. "Good concordance between patients and their non-professional carers about factors associated with a ‘good death’ and other important end-of-life decisions". BMJ Supportive & Palliative Care 9, nr 3 (17.05.2016): 340–45. http://dx.doi.org/10.1136/bmjspcare-2015-001085.
Pełny tekst źródłaLarkin, Mary, i Alisoun Milne. "Carers and Empowerment in the UK: A Critical Reflection". Social Policy and Society 13, nr 1 (18.06.2013): 25–38. http://dx.doi.org/10.1017/s1474746413000262.
Pełny tekst źródłaEwing, Gail, Sarah Croke, Christine Rowland i Gunn Grande. "14 Enabling tailored and coordinated support for family carers of people with motor neurone disease through adaptation of a carer support needs assessment tool (CSNAT) intervention". BMJ Supportive & Palliative Care 8, nr 3 (wrzesień 2018): 365.1–365. http://dx.doi.org/10.1136/bmjspcare-2018-mariecurie.14.
Pełny tekst źródłaBraham, Meg, i Mary Banks. "Who cares for the carers?" Nursing Standard 2, nr 31 (7.05.1988): 13. http://dx.doi.org/10.7748/ns.2.31.13.s55.
Pełny tekst źródłaArmon, Carmel. "Who cares for the carers?" Amyotrophic Lateral Sclerosis 7, nr 3 (styczeń 2006): 131. http://dx.doi.org/10.1080/14660820600600384.
Pełny tekst źródłaKelly, Mike. "WHO CARES…………FOR THE CARERS?" Journal of Renal Care 36, nr 1 (marzec 2010): 16–20. http://dx.doi.org/10.1111/j.1755-6686.2010.00139.x.
Pełny tekst źródłaWilliams, Tracey. "Who cares for the carers?" Journal of Perioperative Practice 29, nr 7-8 (27.06.2019): 195. http://dx.doi.org/10.1177/1750458919858862.
Pełny tekst źródłaD'Cruz, L. "Who cares for the carers?" British Dental Journal 207, nr 1 (lipiec 2009): 11–12. http://dx.doi.org/10.1038/sj.bdj.2009.557.
Pełny tekst źródłaSturge, C., A. Frank i T. Coster. "Who cares for young carers?" BMJ 308, nr 6942 (4.06.1994): 1510–11. http://dx.doi.org/10.1136/bmj.308.6942.1510b.
Pełny tekst źródłaTravis, M. J., i T. Bruce. "Who cares for young carers?" BMJ 309, nr 6950 (30.07.1994): 341. http://dx.doi.org/10.1136/bmj.309.6950.341a.
Pełny tekst źródłaJenkins, S., i C. Wingate. "Who cares for young carers?" BMJ 308, nr 6931 (19.03.1994): 733–34. http://dx.doi.org/10.1136/bmj.308.6931.733.
Pełny tekst źródłaPilkington, Paulina. "Who Cares for the Carers?" Journal of Advanced Nursing 18, nr 12 (grudzień 1993): 1855–56. http://dx.doi.org/10.1046/j.1365-2648.1993.18121855.x.
Pełny tekst źródłaFuller, Alice. "Who cares for the carers?" British Journal of Neuroscience Nursing 8, nr 5 (październik 2012): 311. http://dx.doi.org/10.12968/bjnn.2012.8.5.311.
Pełny tekst źródłaDiminic, S., E. Hielscher, M. G. Harris, Y. Y. Lee, J. Kealton i H. A. Whiteford. "A profile of Australian mental health carers, their caring role and service needs: results from the 2012 Survey of Disability, Ageing and Carers". Epidemiology and Psychiatric Sciences 28, nr 6 (31.08.2018): 670–81. http://dx.doi.org/10.1017/s2045796018000446.
Pełny tekst źródłaGresswell, I., L. Lally, D. Adamis i G. M. McCarthy. "Widening the net: exploring social determinants of burden of informal carers". Irish Journal of Psychological Medicine 35, nr 1 (23.08.2017): 43–51. http://dx.doi.org/10.1017/ipm.2017.36.
Pełny tekst źródłaKouroupa, A., E. Petkari i D. Giacco. "Carer involvement in the transition from inpatient to community mental healthcare: Experiences of stakeholders". European Psychiatry 65, S1 (czerwiec 2022): S610. http://dx.doi.org/10.1192/j.eurpsy.2022.1563.
Pełny tekst źródłaPerera, Sharnel Miriam, Clare O’Callaghan, Anna Ugalde, Olinda Santin, Cassandra Beer, G. Prue, Katherine Lane, Gerard G. Hanna i Penelope Schofield. "Codesigning a supportive online resource for Australian cancer carers: a thematic analysis of informal carers’ and healthcare professionals’ perspectives about carers’ responsibilities and content needs". BMJ Open 11, nr 10 (październik 2021): e055026. http://dx.doi.org/10.1136/bmjopen-2021-055026.
Pełny tekst źródłaBruce, Remia, Wendy Murdoch, Ashley Kable, Kerrin Palazzi, Carolyn Hullick, Dimity Pond, Christopher Oldmeadow i in. "Evaluation of Carer Strain and Carer Coping with Medications for People with Dementia after Discharge: Results from the SMS Dementia Study". Healthcare 8, nr 3 (31.07.2020): 248. http://dx.doi.org/10.3390/healthcare8030248.
Pełny tekst źródłaSwan, Susan, Richard Meade i Emma Carduff. "10 Timely identification and support for carers of people at the end of life through the adult carer support plan: triangulating three data sources". BMJ Supportive & Palliative Care 8, nr 3 (wrzesień 2018): 363.2–363. http://dx.doi.org/10.1136/bmjspcare-2018-mariecurie.10.
Pełny tekst źródłaCamden, Andrew, Gill Livingston i Claudia Cooper. "Reasons why family members become carers and the outcome for the person with dementia: results from the CARD study". International Psychogeriatrics 23, nr 9 (1.07.2011): 1442–50. http://dx.doi.org/10.1017/s1041610211001189.
Pełny tekst źródłaKuipers, E., P. Bebbington, G. Dunn, D. Fowler, D. Freeman, P. Watson, A. Hardy i P. Garety. "Influence of carer expressed emotion and affect on relapse in non-affective psychosis". British Journal of Psychiatry 188, nr 2 (luty 2006): 173–79. http://dx.doi.org/10.1192/bjp.bp.104.007294.
Pełny tekst źródłaLinacre, Stephen, Suzanne Heywood-Everett, Vishal Sharma i Andrew J. Hill. "Comparing carer wellbeing: implications for eating disorders". Mental Health Review Journal 20, nr 2 (8.06.2015): 105–18. http://dx.doi.org/10.1108/mhrj-12-2014-0046.
Pełny tekst źródłaLalor, A., K. Ip i D. Parikh. "P065 Sleep Perceptions of Carers in Palliative Care: A Qualitative Study". SLEEP Advances 3, Supplement_1 (1.10.2022): A51. http://dx.doi.org/10.1093/sleepadvances/zpac029.136.
Pełny tekst źródłaJackson, Haley, Jane Wray, Eric Gardiner i Tracy Flanagan. "Involving carers in risk assessment: a study of a structured dialogue between mental health nurses and carers". Journal of Research in Nursing 24, nr 5 (sierpień 2019): 330–41. http://dx.doi.org/10.1177/1744987119851533.
Pełny tekst źródłaCormac, Irene, i Peter Tihanyi. "Meeting the mental and physical healthcare needs of carers". Advances in Psychiatric Treatment 12, nr 3 (maj 2006): 162–72. http://dx.doi.org/10.1192/apt.12.3.162.
Pełny tekst źródłaRaune, D., E. Kuipers i P. E. Bebbington. "Expressed emotion at first-episode psychosis: investigating a carer appraisal model". British Journal of Psychiatry 184, nr 4 (kwiecień 2004): 321–26. http://dx.doi.org/10.1192/bjp.184.4.321.
Pełny tekst źródłaCooper, Claudia, Julie Barber, Mark Griffin, Penny Rapaport i Gill Livingston. "Effectiveness of START psychological intervention in reducing abuse by dementia family carers: randomized controlled trial". International Psychogeriatrics 28, nr 6 (11.12.2015): 881–87. http://dx.doi.org/10.1017/s1041610215002033.
Pełny tekst źródłaEwing, Gail, Sarah Croke, Christine Rowland i Gunn Grande. "Suitability and acceptability of the Carer Support Needs Assessment Tool (CSNAT) for the assessment of carers of people with MND: a qualitative study". BMJ Open 10, nr 12 (grudzień 2020): e039031. http://dx.doi.org/10.1136/bmjopen-2020-039031.
Pełny tekst źródłaSzmukler, George I., Til Wykes i Sue Parkman. "Care-giving and the impact on carers of a community mental health service". British Journal of Psychiatry 173, nr 5 (listopad 1998): 399–403. http://dx.doi.org/10.1192/bjp.173.5.399.
Pełny tekst źródłaEwing, Gail, Lynn Austin, Debra Jones i Gunn Grande. "Who cares for the carers at hospital discharge at the end of life? A qualitative study of current practice in discharge planning and the potential value of using The Carer Support Needs Assessment Tool (CSNAT) Approach". Palliative Medicine 32, nr 5 (28.02.2018): 939–49. http://dx.doi.org/10.1177/0269216318756259.
Pełny tekst źródłaHennings, J., K. Froggatt i J. Keady. "Approaching the end of life and dying with dementia in care homes: the accounts of family carers". Reviews in Clinical Gerontology 20, nr 2 (22.04.2010): 114–27. http://dx.doi.org/10.1017/s0959259810000092.
Pełny tekst źródłaMarques, Maria J., Bob Woods, Eva Y. L. Tan, Marjolein de Vugt i Frans Verhey. "325 - Relationship quality in dementia: Preliminary longitudinal analyses of the EU-JPND Actifcare cohort study". International Psychogeriatrics 32, S1 (październik 2020): 83. http://dx.doi.org/10.1017/s1041610220002252.
Pełny tekst źródłaMalm, Camilla, Stefan Andersson, Håkan Jönson, Lennart Magnusson i Elizabeth Hanson. "Moving beyond the first response phenomenon". International Journal of Sociology and Social Policy 39, nr 7/8 (22.08.2019): 627–43. http://dx.doi.org/10.1108/ijssp-05-2019-0091.
Pełny tekst źródłaBosboom, Pascalle R., Helman Alfonso, Joanna Eaton i Osvaldo P. Almeida. "Quality of life in Alzheimer's disease: different factors associated with complementary ratings by patients and family carers". International Psychogeriatrics 24, nr 5 (16.01.2012): 708–21. http://dx.doi.org/10.1017/s1041610211002493.
Pełny tekst źródłaDarley, Sarah, Sarah Knowles, Kate Woodward-Nutt, Claire Mitchell, Gunn Grande, Gail Ewing, Sarah Rhodes, Audrey Bowen i Emma Patchwood. "Challenges implementing a carer support intervention within a national stroke organisation: findings from the process evaluation of the OSCARSS trial". BMJ Open 11, nr 1 (styczeń 2021): e038129. http://dx.doi.org/10.1136/bmjopen-2020-038129.
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