Thematische Bibliographien / Health Care7

Auswahl der wissenschaftlichen Literatur zum Thema „Health Care7“

Autor: Grafiati
Veröffentlicht am 26. Juli 2024

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Zeitschriftenartikel zum Thema "Health Care7"

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Krishna Kotha, Hari. „Analyzing the Role of Health Apps in Promoting Healthy Lifestyle and Preventive Care“. International Journal of Science and Research (IJSR) 12, Nr. 11 (05.11.2023): 903–10. http://dx.doi.org/10.21275/sr231111061822.

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Cui, Zhenyu, und Nobuo Akai. „Corruption, Political Stability and Efficiency of Government Expenditure on Health Care: Evidence fromAsian Countries“. Central Asian Review of Economics & Policy 1, Nr. 3 (2019): 1–18. http://dx.doi.org/10.15604/carep.2019.01.03.001.

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Cunha, Sidney Miguel Mesquita da, Valéria Regina Maciel da Silva, Carla Viana Dendasck, Elisângela Claudia de Medeiros Morais, Margaret de Oliveira und Euzébio de Oliveira. „Occupational Stress of the Nursing Team that works in the Intensive Care Unit“. Revista Científica Multidisciplinar Núcleo do Conhecimento 04, Nr. 11 (23.11.2017): 68–78. http://dx.doi.org/10.32749/nucleodoconhecimento.com.br/health/intensive-care-unit.

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Ans, Muhammad, Mujahid Hussain, Fahad Ahmed, Kalsoom Jehan Khan, Sameen Abbas und Muhammad Sultan. „Umbilical Cord Care Practices and Cord Care Education of Mothers Attending Health Care (Pakistan Prospect)“. Health 15, Nr. 01 (2023): 20–32. http://dx.doi.org/10.4236/health.2023.151002.

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Lavrador, José Pedro, Nuno Simas, Edson Oliveira, Joaquim Cruz Teixeira, Diogo Simão und Sérgio Livraghi. „Discogenic pain: Who cares?“ Health 05, Nr. 11 (2013): 1929–37. http://dx.doi.org/10.4236/health.2013.511261.

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Majamanda, Maureen Daisy, Tiwonge Ethel Mbeya Munkhondya, Miriam Simbota und Maria Chikalipo. „Family Centered Care versus Child Centered Care: The Malawi Context“. Health 07, Nr. 06 (2015): 741–46. http://dx.doi.org/10.4236/health.2015.76088.

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Silva, Isabelle Christine Fonsêca G. A., Tainara Lôrena dos Santos Ferreira, Dídia de Oliveira Pereira, Joymara Railma Gomes de Assunção, Paloma Batista Costa, Jovanka Bittencourt Leite de Carvalho, Iris do Ceu Clara Costa und Fábia Barbosa de Andrade. „Maternal and Child Care Assessment Focused on Prenatal Care and Birth“. Health 07, Nr. 01 (2015): 167–73. http://dx.doi.org/10.4236/health.2015.71019.

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dos Santos Ferreira, Tainara Lôrena, Tiago José Barbosa de Andrade, Janio Gustavo Barbosa, Iris do Ceu Clara Costa und Fábia Barbosa de Andrade. „Evaluation of Quality Care for Senior Citizens in Primary Health Care“. Health 07, Nr. 09 (2015): 1069–74. http://dx.doi.org/10.4236/health.2015.79121.

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de Andrade, Fábia Barbosa, Iris do Ceu Clara Costa, Tainara Lôrena dos Santos Ferreira, Isabelle Christine Fonsêca G. A. Silva, Íngrid Katianne Marques Araújo, Dídia de Oliveira Pereira, Joymara Railma Gomes de Assunção, Jéssica Isabelle dos Santos Dutra und Aline de Lima Cabral. „Assessment of Comprehensive Health Care of the Elderly in Primary Health Care“. Health 07, Nr. 03 (2015): 365–70. http://dx.doi.org/10.4236/health.2015.73041.

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Hamabata, Kenji, Hideyuki Shiotani und Keiko Sekido. „Interprofessional Work Model for Dementia Care in Hospitals for Community-Based Care“. Health 12, Nr. 12 (2020): 1543–61. http://dx.doi.org/10.4236/health.2020.1212112.

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Dissertationen zum Thema "Health Care7"

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Basu, Rashmita. „Healthy lifestyle, disease prevention and health care utilization“. Pullman, Wash. : Washington State University, 2009. http://www.dissertations.wsu.edu/Dissertations/Fall2009/r_basu_112309.pdf.

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Annear, Peter Leslie, und mikewood@deakin edu au. „Healthy markets - Heathly people? Reforming health care in Cambodia“. Deakin University. School of Health Sciences, 2001. http://tux.lib.deakin.edu.au./adt-VDU/public/adt-VDU20050825.134836.

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Health care reform has been described as a global epidemic. This thesis deals with nature and experience of health care reform in developing countries. Increasing privatisation, economic transition, and structural adjustment have provided the context for health system changes. Different approaches to reform have been developed by international organisations such as the World Bank, WHO and UNICEF. What has driven national health care reforms? Are such policies really appropriate to developing countries? Has a consensus now emerged in relation to international health policy? Has a new health care ‘model’ appeared? The study of health care reform in Cambodia is a timely opportunity to investigate the implementation of health care reform under extreme conditions. These conditions include a legacy of genocide, long-term conflict, political isolation, and economic transition. This case study uses both qualitative and quantitative methods and multiple sources of data to analyse the reform program. The study reinforces the conclusion that, under conditions of extreme poverty, market based reforms are likely to have limited positive impact. Rather, understanding the cultural conditions that determine demand, delivering health care of a satisfactory quality, providing appropriate incentives for health practitioners, and supporting services with adequate public funding are the prerequisites for improved service delivery and utilisation. Cambodia's strategy of integrated district health service development and universal population coverage may provide an instructive example of reform. Emerging policy issues identified by this case study include the fundamental role of equity in service provision, the influence of the social determinants of health and illness and interest in the appropriate use of evidence in international health policy-making.
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Skånér, Ylva. „Diagnosing heart failure in primary health care /“. Stockholm, 2004. http://diss.kib.ki.se/2004/91-7349-784-3/.

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Spears, Amanda. „The Healthy People 2010 criteria for the care of children with special health care needs an effective national policy for meeting mental health care needs? /“. CONNECT TO ELECTRONIC THESIS, 2007. http://dspace.wrlc.org/handle/1961/4128.

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Tansathitaya, Vimolmas. „Selected Health Related Factors and Behaviors among Southeast Asian Immigrants: Tobacco, Mental Health, Healthy Neighborhood Factors, and Health Care Utilization“. University of Cincinnati / OhioLINK, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1552391701300341.

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Holsapple, Susan Wilt. „Heal this health care experiences of gay men /“. Related Electronic Resource: Current Research at SU : database of SU dissertations, recent titles available full text, 2005. http://wwwlib.umi.com/cr/syr/main.

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Haas, Marion Ruth. „Benefits of health care beyond health: an exploration of non-health outcomes of health care“. University of Sydney. Public Health, 2002. http://hdl.handle.net/2123/854.

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Recent interest in identifying and measuring health outcomes represents an advance in our understanding of how health care for individuals should be evaluated. However, the concept of health outcomes has mainly focussed on improvements in health status. Non-health outcomes of health care may also be important to patients. In this thesis, four tasks were undertaken with the aim of identifying non-health outcomes and establishing the extent of their relevance and importance to patients. First, the illness experience literature was reviewed to identify potential non-health outcomes. Seven categories of non-health outcomes were identified: information, being treated with dignity, being able to trust the health care provider, having distress recognised and supported, participating in decision making, legitimation and reassurance. Second, to gain an in-depth understanding of these concepts, topic-specific literature was reviewed and synthesised. Third, in order to confirm how relevant and important the concepts were to patients, a qualitative study was conducted with each of two different groups of health service users. Broadly, patients considered that all the non-health concepts were relevant, although the extent to which they were important varied. Fourth, to test the relative importance of the seven concepts, a Stated Preference Discrete Choice experiment in the context of general practice was conducted. This study showed that most people thought their GP demonstrated behaviour likely to result in the production of non-health outcomes. The results showed that although all the non-health outcomes were, to some extent, preferred by respondents, trust was most important, followed by legitimation and recognition of and support for emotional distress. Once again, these results point to the importance of context in the evaluation of health care from the patient's perspective. While still being perceived as positive aspects of health care, the provision of information and acting autonomously or participating in decisions about their health care were the non-health outcomes considered least important by patients
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Mbuzi, Vainess Banda. „Understanding Indigenous people’s experiences of acute health care with a focus on heart health“. Phd thesis, Australian Catholic University, 2020. https://acuresearchbank.acu.edu.au/download/40626310ee5a3fd6023840c44f246c2c91a0e6cda381bd74a9f0e71e00725fec/16415877/Mbuzi_2020_Indigenous_People%27s_Experiences_Focus_On_Heart_Health.pdf.

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Overview The program of research presented in this thesis was designed to increase understanding of the central issues related to Indigenous peoples’ hospitalisation experiences. Emphasis was given to Indigenous peoples’ cardiovascular health care. This area was chosen because cardiovascular disease has been described as one of the major contributors to the health disparity between Indigenous and non-indigenous peoples in Australia. This was of interest to me because the main study setting is a cardiothoracic hospital. This hospital is the largest referral centre for cardiac conditions in Queensland, surrounding states, and neighbouring countries, including Papua New Guinea. This program of research comprised four studies. The first study, a metasynthesis, was undertaken to gather a worldwide perspective of Indigenous peoples’ experiences of acute care. In the second study, a narrative inquiry was undertaken. It focused on Indigenous Australians’ experiences of acute cardiac care. The third study was a systematic review. It adopted a broader perspective to investigate the effectiveness of Australian Indigenous cardiovascular health programs. The final study, an autoethnography, utilised reflective inquiry to examine issues related to researching with Indigenous people. Background There are many explanations given to explicate sources of health disparities for Indigenous people. Most of the factors have their roots in past colonialism and its policies. Past practices by former Australian governments devalued the Indigenous culture, tortured individuals both physically and psychologically, and effectively marginalised the Indigenous population. Indigenous people still experience elements of tacit and overt discriminatory practices within the healthcare system. A range of cultural and Indigenous-specific factors also impact Indigenous health in a negative way. As a result, Australian Indigenous people encounter noteworthy health inequalities when compared to non-Indigenous Australians. In recognition and response to this disparity in health status, the Australian government launched a “Close the Gap” campaign in 2008. The campaign attempts to narrow the health differences and life expectancy, while also considering other factors that impact Indigenous health such as education and employment opportunities. Coming to hospital is a challenge for most Indigenous Australians. In Australia, Indigenous people are often geographically isolated in scattered settlements, and living in relatively small communities, leading to fragmented services and support for health and social programs. They are isolated both geographically and culturally when they come to hospital. In most cases, they have to relocate in order to access the services they need. This experience can be overwhelming due to the different culture of hospital practices and world views of healthcare professionals, who are mainly from westernised backgrounds. In most healthcare settings, Indigenous peoples’ culture and views of health have not been integrated into mainstream health. In a way, Indigenous people are forced to leave their way of life at home and adapt to western culture when hospitalised. This can cause discomfort for Indigenous people in many ways. As a result, some avoid accessing health services even when such services are needed and are available to them. A few aspects of Indigenous culture may be presented in hospital settings but usually at tokenistic or symbolic levels. This includes items such as flags at the front of the hospital and Indigenous paintings on display. Health professionals’ attitudes, as well as the hospital policies that guide their practice, do not usually accommodate Indigenous values into practice. Bedside manners and ward practices have remained the same for many years – fashioned and practiced in the ways of the dominant culture. In Australia, cardiovascular disease is known to constitute one of the major single causes of ill health and death for Indigenous peoples. As a result, it contributes significantly to life expectancy differentials between this population and other Australians. Indigenous Australians suffer major gaps in health status even when compared with other Indigenous peoples in other first-class nations. This includes Indigenous peoples from Canada, New Zealand and the United States of America. Health practitioners, therefore, need to be aware and proactively act on the underlying causes of poor health outcomes among Indigenous people. Methods Four studies were conducted over the period of this program of research using qualitative and quantitative research methods. The first study was a metasynthesis of qualitative research studies. Its aim was to investigate current evidence of Indigenous peoples’ hospital experiences in order to summarise current knowledge. Systematic procedures were employed to retrieve studies from the period between 2000 to 2016. The review process was conducted following Joanna Briggs Institute (2014) guidelines for conducting systematic review and synthesis of qualitative data. The second study utilised narrative inquiry, a qualitative methodology in which face to face interviews were used to enable participants to recount their experiences of hospitalisation. Narrative inquiry was selected specifically because it involves storytelling, which is culturally familiar to Indigenous people. The aim was to explore Indigenous peoples’ experiences of hospitalisation of acute cardiac care. To accomplish this, data were collected using a purposeful sample of Indigenous cardiac participants: all Indigenous patient participants had been hospitalised for acute cardiac care. The third study was a systematic review. Its aim was to investigate the effectiveness of cardiovascular health care programs designed for Indigenous Australians. Analysis of the strategies that were used to achieve successful outcomes was conducted. Studies that used experimental designs and reported interventions or programs explicitly aimed at improving Indigenous cardiovascular health were considered for inclusion. The search period was between 2008 to 2017. The fourth study was an autoethnography. This study involved use of personal diary-based data and reflective inquiry to present a researcher perspective of the experience of conducting research with Indigenous people. The aim was to share the experience to inform others of aspects for consideration when conducting research with Indigenous participants. The purpose was to offer a true picture of conducting research from my perspective. The study enabled examination of the interplay of my personal, social, professional life and how these impact on my clinical and research practice. Findings The metasynthesis revealed that overall, Indigenous peoples, worldwide, have remained in a disadvantaged position when it comes to their health and wellbeing. Several factors were identified that contribute to widespread inequality in Indigenous healthcare. It was increasingly clear that current healthcare systems are not effectively working well in addressing Indigenous peoples’ health needs. The findings of the narrative inquiry indicated that three themes characterised Indigenous peoples’ experiences of hospitalisation which were as follows: the impact of the past, reality of the present, and anticipating the future in Australia. Hospitalisation remains a challenge for Indigenous peoples. This is due to a sense of dislocation and lack of cultural and spiritual aspects to care, as well as the persisting poor relational interactions encountered. Quantitative research studies that implemented interventions targeted for management of cardiac conditions among Indigenous population within Australia were included in the systematic review. The results revealed that there were limited published studies targeted specifically towards Indigenous Australians’ cardiac health improvement. However, positive outcomes were reported in terms of achieving clinical targets. Physical aspects such as blood pressure reduction, exercise attendance, and enhancing cardiac health knowledge in biomedical interventions for the Indigenous communities were the main focus. The autoethnography revealed that with adequate preparation and involvement of Indigenous people the research process can be made easier. Again, because of past experiences which have led Indigenous people to be over researched with little feedback to them; researching this population group is challenging. Most researchers in the past have conducted research that has not effectively benefited the community. In some cases, research outcomes have misrepresented participants through use of methodologies that are not appropriate for Indigenous peoples. It is not unusual for Indigenous peoples to view the word “research” as a “dirty” word that brings uncomfortable feelings. In some instances, Indigenous participants have not seen its benefits of the research or understood the outcomes. Conclusions In summary, the program of research appraised current evidence. Further, it presented new knowledge that can inform and support practitioners in their quest to progress Indigenous peoples’ healthiness and welfare. Highlighting issues from Indigenous peoples ’perspectives can facilitate development of a better understanding of issues that impact their experiences with healthcare institutions. Such revelations can help in the identification of limitations faced by health professionals or constraints they encounter in the delivery of healthcare among Indigenous people. This could assist in revealing issues that are barriers to being effective in designing and implementing effective strategies to improve Indigenous health and wellbeing. Further research is warranted to follow up on the issues identified in this research.
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Sanchez, Collado Irene. „The impact of providing informal care on carer well-being, retirement, and health“. Thesis, University of York, 2017. http://etheses.whiterose.ac.uk/20049/.

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This thesis includes a series of case studies exploring the impact of providing informal (unpaid) care on the well-being, retirement decisions, and physical and mental health outcomes of carers. We use a representative sample of the UK population and informal carers from eighteen waves of the British Household Survey (BHPS). Analysis is undertaken from an economic and micro-econometrics perspective, using a variety of econometric techniques tailored to the specific questions and data in each study. The first chapter introduces the topics and provides descriptive statistics of the sample of carers in BHPS. In the second chapter, we study the impact of providing informal care on happiness and life satisfaction and calculate monetary values for informal care for each of these subjective well-being measures and by gender. We find monetary values of around £18 per extra hour of informal care provided per week for men and women in our preferred model, although values vary with the well-being measure, the measure of informal care, and the estimation method used. In chapter three we study whether the decision to retire before the State Pension Age is affected by the intensity of the informal care provided by men and women. We find that the probability of retirement is around twice as high for carers than for non-carers. Chapter 4 analyses the impact of providing informal care on caregiver ́s health, using a variety of health measures: GHQ, SF-6D, health conditions and self-assessed health. We find a small but negative effect of providing informal care on both the physical and mental health of informal carers. With these analyses, we aim to contribute to the literature by providing evidence on the impact of informal caring on carers to inform policy towards them and those they care for.
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Bataineh, Hana. „An Empirical Investigation of Unmet Health Care, Health Care Utilization and Health Outcomes“. Thesis, Université d'Ottawa / University of Ottawa, 2017. http://hdl.handle.net/10393/36492.

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This thesis is comprised of three chapters that empirically examine two important areas in health economics: access to health care and health outcomes. The first chapter explores the impact of health care utilization on unmet health care needs (UHC) using four biennial confidential master files (2001-2010) of the Canadian Community Health Survey and applying an instrumental variables (IV) approach to deal with the endogeneity of health care utilization. The presence of drug insurance and the number of physicians in each health region are used to identify the causal effect. I find a clear and robustly negative relationship between health care use and unmet health care needs; individuals who are more likely to report unmet health care needs are those who use the health care system less frequently. One more visit to a family doctor, specialist or a medical doctor on average, decreases the probability of having unmet health care needs by 7.1, 4.6 and 2.8 percentage points, respectively. Further analysis by sub groups reveals that the impact of health care utilization on UHC is larger for females in comparison to males, rural residents in comparison to urban dwellers and those with low household income rather than high. The second chapter of this thesis examines whether the presence of the unmet health-care (UHC) needs has an adverse effect on health outcomes using the National Population Health Survey, a nationally representative longitudinal data set spanning 18 years. I pay close attention to the potential endogeneity of this problem. Five direct and indirect measures of health-related outcomes are examined. I find clear and robust evidence that the presence of UHC either two-years previously or anytime in the past, affects negatively the current health of the individual – controlling for a host of other influences. For instance, reporting UHC in the previous cycle reduces the probability of being in excellent or very good health and in good mental health, respectively by 8.1 and 1.2 percentage points; it reduces the HUI3 score by 2.9 percentage points and increases the expected number of medications used by 11%. Further analysis by looking at the effect of UHC when it was due to accessibility reasons, reveal that the effect of UHC because of accessibility reasons on health outcomes is larger than the one of the overall UHC, but the difference is small in general. Finally, the third chapter of this thesis examines the link between social networks and access to health care utilization, focusing particularly on the probability of having a regular family doctor. Unlike previous work that uses cross sectional data, I use panel data from the National Population Health survey to control for unobserved heterogeneity. Access to a regular family doctor is modeled using the dynamic random effects probit model, which makes it possible to explore the dynamics of access to a regular family doctor– for instance, the role played by past access status to a family doctor in predicting current access. In particular, I use the dynamic random effects probit model that controls for both unobserved heterogeneity and for initial conditions effects. I find robust evidence of a highly statistically significant relationship between social capital and the probability of having a regular family doctor. Although the marginal effects are modest, the results from all model specifications show that there is clear evidence that individuals with high levels of tangible, affection, emotional, social interaction, who live with spouse only or with spouse and children are more likely to have a regular family doctor, whereas those living alone are less likely to have a regular family doctor. The results also reveal that past access to a family doctor is an important determinant for both current and future access. The predicted probability of having a regular family doctor is about 18 percentage points (or 20%) higher for individuals who had a family doctor in the previous period, relative to those who did not. In addition, I find that unobserved heterogeneity accounts for about 25% of the variation in accessing a regular family doctor and is significantly correlated with the access to a family doctor over my long panel.
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Bücher zum Thema "Health Care7"

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Downie, R. S. Healthy respect: Ethics in health care. 2. Aufl. Oxford: Oxford University Press, 1994.

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Downie, R. S. Healthy respect: Ethics in health care. London: Faber, 1987.

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United States. Department of Veterans Affairs. Women veterans health care: Healthy aging. Washington, D.C: Dept. of Veterans Affairs, 2010.

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Lumby, Judy. Who cares?: The changing health care system. Crows Nest, N.S.W: Allen & Unwin, 2001.

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Health, Saskatchewan Saskatchewan, Hrsg. A health research strategy, Saskatchewan: Healthy people, a healthy province. [Regina, Sask.]: Saskatchewan Health, 2005.

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Health, Ontario Ministry of. 2004 Chief Medical Officer of Health Report: Healthy weights, healthy lives. Toronto: Ministry of Health and Long-Term Care, 2004.

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Maev-Ann, Wren, Hrsg. How Ireland cares: The case for health care reform. Dublin: New Island, 2006.

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Fries, Christopher J. (Christopher John), Hrsg. Pursuing health and wellness: Healthy societies, healthy people. Don Mills, Ont: Oxford University Press, 2011.

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Center, International Longevity, Canyon Ranch Health Resort und Alliance for health and the Future., Hrsg. Promoting men's health: Addressing barriers to healthy lifestyle and preventive health care. New York, NY: International Longevity Center-USA, 2004.

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British Institute of Learning Disabilities., Hrsg. Health care to match health care needs. Kidderminster: BILD, 2003.

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Buchteile zum Thema "Health Care7"

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Zimring, Craig, und Jennifer DuBose. „Healthy Health Care Settings“. In Making Healthy Places, 203–15. Washington, DC: Island Press/Center for Resource Economics, 2011. http://dx.doi.org/10.5822/978-1-61091-036-1_13.

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Lowe, Rodney. „Health Care“. In The Welfare State in Britain since 1945, 163–92. London: Macmillan Education UK, 1993. http://dx.doi.org/10.1007/978-1-349-22549-1_7.

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Orbell, Sheina, Havah Schneider, Sabrina Esbitt, Jeffrey S. Gonzalez, Jeffrey S. Gonzalez, Erica Shreck, Abigail Batchelder et al. „Health Care“. In Encyclopedia of Behavioral Medicine, 908. New York, NY: Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4419-1005-9_884.

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Hauck, Fern R. „Health Care“. In Encyclopedia of Immigrant Health, 768–74. New York, NY: Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4419-5659-0_594.

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Ward, Ivy M., M. Annette Ketner, Donna B. Tower, Mary L. Hicks, Len Van Noord, Andrea N. Beal, Janice Hendricks et al. „Health Care“. In Direct Mail Fund Raising, 153–77. Boston, MA: Springer US, 1988. http://dx.doi.org/10.1007/978-1-4899-3799-5_5.

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DeWitt, Larry, und Edward D. Berkowitz. „Health Care“. In A Companion to Lyndon B. Johnson, 163–86. Oxford, UK: Wiley-Blackwell, 2011. http://dx.doi.org/10.1002/9781444347494.ch10.

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Walshe, Grahame, und Peter Daffern. „Health Care“. In Managing Cost-Benefit Analysis, 39–71. London: Macmillan Education UK, 1990. http://dx.doi.org/10.1007/978-1-349-20763-3_2.

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Lowe, Rodney. „Health Care“. In The Welfare State in Britain since 1945, 167–97. London: Macmillan Education UK, 1999. http://dx.doi.org/10.1007/978-1-349-27012-5_7.

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Mphande, Fingani Annie. „Health care“. In Infectious Diseases and Rural Livelihood in Developing Countries, 87–113. Singapore: Springer Singapore, 2016. http://dx.doi.org/10.1007/978-981-10-0428-5_6.

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Ryan, Michael, und Richard Prentice. „Health Care“. In Social Trends in the Soviet Union from 1950, 85–97. London: Palgrave Macmillan UK, 1987. http://dx.doi.org/10.1007/978-1-349-18883-3_9.

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Konferenzberichte zum Thema "Health Care7"

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Nirwal, Neha, Neetu Sardana und Arpita Jadhav Bhatt. „Hopeful hearts: A mobile health care application“. In 2014 Seventh International Conference on Contemporary Computing (IC3). IEEE, 2014. http://dx.doi.org/10.1109/ic3.2014.6897199.

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Okeke, Fabian, Emily Tseng, Benedetta Piantella, Mikaela Brown, Harveen Kaur, Madeline R. Sterling und Nicola Dell. „Technology, home health care, and heart failure“. In the 2nd ACM SIGCAS Conference. New York, New York, USA: ACM Press, 2019. http://dx.doi.org/10.1145/3314344.3332487.

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3

Chen, Heng-Shuen, Mei-Ju Su, Tsung-Hsueh Tsai, Shih-Shung Teng, Han-Wei Zhang, Jin-Shin Lai, Fei-Pei Lai und Ching-Yu Chen. „U-Care for the elderly: Implemenation of a Comprehensive Living and Health Care Network“. In 2007 9th International Conference on e-Health Networking, Application and Services. IEEE, 2007. http://dx.doi.org/10.1109/health.2007.381627.

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4

Venkateswarlu, D. S., K. S. Verma und K. S. R. A. Murthy. „e Health networking to cater to Rural Health Care and Health Care for the Aged“. In 2007 9th International Conference on e-Health Networking, Application and Services. IEEE, 2007. http://dx.doi.org/10.1109/health.2007.381649.

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5

Trindade, I. G., J. Lucas, R. Miguel, P. Alpuim, M. Carvalho und N. M. Garcia. „Lightweight portable sensors for health care“. In 2010 12th IEEE International Conference on e-Health Networking, Applications and Services (Healthcom 2010). IEEE, 2010. http://dx.doi.org/10.1109/health.2010.5556575.

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6

Tsai, A., P. H. Kuo, G. Lee und Ming-Sung Lin. „Electronic Clinical Guidelines for Intensive Care Unit“. In 2007 9th International Conference on e-Health Networking, Application and Services. IEEE, 2007. http://dx.doi.org/10.1109/health.2007.381616.

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7

Hoang, D. B., E. Lawrence, N. F. Ahmad, V. Balasubramanian, C. Homer, M. Foureur und N. Leap. „Assistive care loop with electronic maternity records“. In 2008 10th International Conference on e-health Networking, Applications and Services (Healthcom). IEEE, 2008. http://dx.doi.org/10.1109/health.2008.4600121.

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8

Ahmad, Nor Faizah, Doan B. Hoang und M. Hoang Phung. „Robust preprocessing for health care monitoring framework“. In 2009 11th International Conference on e-Health Networking, Applications and Services (Healthcom 2009). IEEE, 2009. http://dx.doi.org/10.1109/health.2009.5406196.

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9

Smith, Stuart T., Amir Talaei-Khoei, Mililani Ray und Pradeep Ray. „Electronic Games for Aged Care and Rehabilitation“. In 2009 11th International Conference on e-Health Networking, Applications and Services (Healthcom 2009). IEEE, 2009. http://dx.doi.org/10.1109/health.2009.5406197.

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10

Pawar, Suvarna, und H. R. Deshmukh. „A Survery on e-Health Care Monitoring for Heart Care Using IOT“. In 2018 International Conference on Inventive Research in Computing Applications (ICIRCA). IEEE, 2018. http://dx.doi.org/10.1109/icirca.2018.8597320.

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Berichte der Organisationen zum Thema "Health Care7"

1

Allen, Roosevelt, Michael Black, William Bray, Douglas W. Butt, Bradley Calhoun, Sylvia Curran, Roger Garay, Sally Kelly, Jeffrey C. Lieb und Kimberly Litherland. Health Care Industry. Fort Belvoir, VA: Defense Technical Information Center, Januar 2007. http://dx.doi.org/10.21236/ada475112.

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2

Brownlee, Shannon, Vikas Saini und Judith Garber. California’s health care paradox: Too much health care spending may lead to poor community health. Lown Institute, Juli 2019. http://dx.doi.org/10.46241/li.tkrn9871.

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3

Turner, Katrina. Mental Health: digital health and remote care. University of Bristol, 2023. http://dx.doi.org/10.37361/sig.2023.1.1.

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4

Brady, Martha, und Beverly Winikoff. Rethinking postpartum health care. Population Council, 1993. http://dx.doi.org/10.31899/rh1.1019.

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5

Brown, Dale, William Knowlton, Irene Kyriakopoulos und Mark McGuire. Health Care Industry Study. Fort Belvoir, VA: Defense Technical Information Center, Januar 2002. http://dx.doi.org/10.21236/ada425482.

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6

Fogel, Robert, und Chulhee Lee. Who Gets Health Care? Cambridge, MA: National Bureau of Economic Research, Juli 2003. http://dx.doi.org/10.3386/w9870.

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7

Gruber, Jonathan. Financing Health Care Delivery. Cambridge, MA: National Bureau of Economic Research, Juli 2022. http://dx.doi.org/10.3386/w30254.

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8

Matteson, Gary N. Health Care Legislation and the Implied U.S. Health Care Policy Through 1992. Fort Belvoir, VA: Defense Technical Information Center, Juni 1996. http://dx.doi.org/10.21236/ada311357.

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9

Rast, Jessica E., Anne M. Roux, Kristy A. Anderson, Lisa A. Croen, Alice A. Kuo, Lindsay L. Shea und Paul T. Shattuck. National Autism Indicators Report: Health and Health Care. A.J. Drexel Autism Institute, Dezember 2020. http://dx.doi.org/10.17918/healthandhealthcare2020.

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Annotation:
Health and health care are critical issues for many children and adults on the autism spectrum. They may experience more frequent use of services and medications. They may need more types of routine and specialty healthcare. And their overall health and mental health care tends to be more complex than people with other types of disabilities and special health care needs. This report provides indicators of health and health care for autistic persons across the lifespan. Topics covered include overall health, health services, medication, insurance, and accessing services. We need to understand health and healthcare needs across the life course to support recommendations on how to improve health and health care at critical points across a person's life. The purpose of this report is to catalogue indicators to aid in decision making to this end.
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Mehegan, Laura. Adults Rate Their Primary Care Health Care Providers. Washington, DC: AARP Research, Oktober 2023. http://dx.doi.org/10.26419/res.00576.001.

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