SwePub
Sök i SwePub databas

  Utökad sökning

Träfflista för sökning "WFRF:(Cunningham Miriam) "

Sökning: WFRF:(Cunningham Miriam)

  • Resultat 1-16 av 16
Sortera/gruppera träfflistan
   
NumreringReferensOmslagsbildHitta
1.
  • Cunningham, Paul, et al. (författare)
  • Assessment of potential ICT-related collaboration and innovation capacity in east Africa
  • 2015
  • Ingår i: 2015 IEEE Global Humanitarian Technology Conference (GHTC). - : IEEE. - 9781467365611 ; , s. 100-107
  • Konferensbidrag (refereegranskat)abstract
    • Due to a significant investment in digital infrastructure and a pro-innovation policy and regulatory framework, the Innovation Ecosystems in Nairobi, Dar es Salaam and Kampala have considerably expanded over the last five years, incorporating new national and international Innovation Stakeholders. This is important in the context of realising the objectives of National Development Plans, and addressing high levels of youth and graduate unemployment. This paper presents a sub-set of results from a comprehensive baseline analysis of Innovation Ecosystems in these cities with a focus on assessing the current level of ICT-related Collaboration, Innovation Absorption capacity and challenges to be addressed. In order to benefit from these developments, it is recommended that the public sector take a leadership role in establishing necessary mechanisms that will stimulate multi-stakeholder collaboration amongst existing Innovation Actors to foster a sustainable Collaborative Open Innovation and Entrepreneurial culture.
  •  
2.
  • Cunningham, Paul, et al. (författare)
  • Baseline Analysis of 3 Innovation Ecosystems in East Africa
  • 2014
  • Ingår i: 2014 International Conference on Advances in ICT for Emerging Regions (ICTer). - 9781479977314 ; , s. 156-162
  • Konferensbidrag (refereegranskat)abstract
    • The potential impact of computing innovations supporting social and economic development (particularly in developing countries) is very dependent on the level of maturity of National Innovation Ecosystems (including policy environment, infrastructure and socio-economic diversification). East Africa has experienced significant growth in ICT-enabled Innovation (particularly mobile) in recent years. Kenya, Tanzania and Uganda have experienced considerable entrepreneurial growth, facilitated by Innovation friendly regulatory environments, evolution of National Research Education Networks (NReNs) and rollout of fibre optic backbones. While it is clear that ICT, Job Creation and developing a Knowledge Economy are common policy priorities, the Innovation Ecosystems in Nairobi, Dar es Salaam and Kampala are quite fragmented. While support for entrepreneurship is improving, Innovation Spaces have sustainability challenges with their business models and there is a limited availability of funding, and training and mentoring for entrepreneurs. Greater collaboration between different stakeholders and more efficient support systems are required to promote accelerated development. In this paper, we provide a survey of the key Innovation Stakeholders in Nairobi, Dar es Salaam and Kampala. This is based on semi-structured face to face interviews (November 2012 – February 2013), supplemented by IST-Africa Surveys, focus group engagement during Research and Innovation Stakeholder workshops, and supported by desk research, follow-up e-mails and telephone interviews to reflect developments up to July 2014.
  •  
3.
  • Cunningham, Paul, et al. (författare)
  • Factors Impacting on the Current Level of Open Innovation and ICT Entrepreneurship in Africa
  • 2016
  • Ingår i: The Electronic Journal of Information Systems in Developing Countries. - : Wiley. - 1681-4835. ; 73
  • Tidskriftsartikel (refereegranskat)abstract
    • Across Africa, Innovation and ICT entrepreneurship are increasingly recognised as important enablers of national and regional socio-economic growth. However, the level of skills capacity, indigenous entrepreneurial expertise and policy support varies considerably. This research study was informed by a semi-structured, moderated focus group involving five public and four education and research stakeholders from eight African Member States. It focused on identifying factors impacting on the current level of open innovation and ICT entrepreneurship in Africa. Organised in Lilongwe, Malawi on 08 May 2015 during IST-Africa Week 2015, a purposive approach was applied to identify the nine informants based on intensity sampling. The results highlighted six main factors: a) level of political will reflected by resource prioritisation; b) alignment with national development plans and associated funding priorities; c) level of understanding of strategic benefits by ministers and senior civil servants; d) level of awareness and sensitization of the general public, e) availability of national innovation and entrepreneurial expertise; and f) willingness and capacity to cooperate with other stakeholders to achieve common goals. Future research will capture perspectives from the private, societal and international donor sectors, and create and validate potential models/methodologies to address the challenges and opportunities identified in this study.
  •  
4.
  • Cunningham, Paul, et al. (författare)
  • Stakeholder Roles and Potential Models to Support Collaborative Open Innovation in East Africa
  • 2015
  • Ingår i: Proceedings of the 13th International Conference on Social Implications of Computers in Developing Countries. - Oslo : University of Oslo. - 9788273684653 ; , s. 63-77
  • Konferensbidrag (refereegranskat)abstract
    • This paper provides an analysis of the Innovation Ecosystems for three representative instances in East Africa: Nairobi (Kenya), Dar es Salaam (Tanzania) and Kampala (Uganda). The authors propose that to maximise the impact of innovation systems in a developing country context, innovation interventions (including ICT4D) must (a) facilitate shared, local ownership, with objectives driven by end-user community needs and taking account of previous interventions, good practices and socio-cultural norms; (b) be co-designed, co-created or adapted in consultation with key Innovation Stakeholders; (c) strengthen the capacity of local beneficiary and/or contributing Stakeholders and (d) address sustainability and wider socio-economic impact after the interventions ends. Innovation (including ICT4D interventions) that do not address these issues run the risk of damaging the local Innovation Ecosystem or breaching trust with local stakeholders, by not taking account of local socio-cultural differences or not adequately addressing expectations raised.
  •  
5.
  •  
6.
  • Cunningham, Miriam (författare)
  • Technology-Enhanced Learning in Kenyan Universities
  • 2016
  • Ingår i: IEEE technology & society magazine. - 0278-0097 .- 1937-416X. ; 35:3, s. 28-35
  • Tidskriftsartikel (refereegranskat)abstract
    • This article discusses some of the findings of a study that bridges an existing knowledge gap by focusing on identifying influences on the wider adoption and uptake of TEL techniques by HEIs in Nairobi. In this context, TEL techniques can encompass e-learning, blended learning, using massive open online courses (MOOCs), or an entirely online course delivery. This study examines why HEIs are using TEL, perceived benefits and challenges of using TEL from an institutional and instructor perspective, and the impact of policies. The findings have important research, practical, societal, and policy making implications for educational delivery on a continent with a rapidly growing population. Findings will assist decision making, inform policy creation, and provide useful foundational reference material for further comparative research in Africa. The lessons learned will also assist tertiary level institutions across the African continent that wish to plan for wider TEL adoption, or to implement TEL in a more effective manner, by considering common challenges that could limit adoption.
  •  
7.
  • De Palma, Adriana, et al. (författare)
  • Predicting bee community responses to land-use changes : effects of geographic and taxonomic biases
  • 2016
  • Ingår i: Scientific Reports. - : Nature Publishing Group. - 2045-2322. ; 6, s. 1-14
  • Tidskriftsartikel (refereegranskat)abstract
    • Land-use change and intensification threaten bee populations worldwide, imperilling pollination services. Global models are needed to better characterise, project, and mitigate bees' responses to these human impacts. The available data are, however, geographically and taxonomically unrepresentative; most data are from North America and Western Europe, overrepresenting bumblebees and raising concerns that model results may not be generalizable to other regions and taxa. To assess whether the geographic and taxonomic biases of data could undermine effectiveness of models for conservation policy, we have collated from the published literature a global dataset of bee diversity at sites facing land-use change and intensification, and assess whether bee responses to these pressures vary across 11 regions (Western, Northern, Eastern and Southern Europe; North, Central and South America; Australia and New Zealand; South East Asia; Middle and Southern Africa) and between bumblebees and other bees. Our analyses highlight strong regionally-based responses of total abundance, species richness and Simpson's diversity to land use, caused by variation in the sensitivity of species and potentially in the nature of threats. These results suggest that global extrapolation of models based on geographically and taxonomically restricted data may underestimate the true uncertainty, increasing the risk of ecological surprises.
  •  
8.
  • Endres, Dominique, et al. (författare)
  • Immunological causes of obsessive-compulsive disorder : is it time for the concept of an "autoimmune OCD" subtype?
  • 2022
  • Ingår i: Translational Psychiatry. - : Springer Nature. - 2158-3188. ; 12:1
  • Forskningsöversikt (refereegranskat)abstract
    • Obsessive-compulsive disorder (OCD) is a highly disabling mental illness that can be divided into frequent primary and rarer organic secondary forms. Its association with secondary autoimmune triggers was introduced through the discovery of Pediatric Autoimmune Neuropsychiatric Disorder Associated with Streptococcal infection (PANDAS) and Pediatric Acute onset Neuropsychiatric Syndrome (PANS). Autoimmune encephalitis and systemic autoimmune diseases or other autoimmune brain diseases, such as multiple sclerosis, have also been reported to sometimes present with obsessive-compulsive symptoms (OCS). Subgroups of patients with OCD show elevated proinflammatory cytokines and autoantibodies against targets that include the basal ganglia. In this conceptual review paper, the clinical manifestations, pathophysiological considerations, diagnostic investigations, and treatment approaches of immune-related secondary OCD are summarized. The novel concept of "autoimmune OCD" is proposed for a small subgroup of OCD patients, and clinical signs based on the PANDAS/PANS criteria and from recent experience with autoimmune encephalitis and autoimmune psychosis are suggested. Red flag signs for "autoimmune OCD" could include (sub)acute onset, unusual age of onset, atypical presentation of OCS with neuropsychiatric features (e.g., disproportionate cognitive deficits) or accompanying neurological symptoms (e.g., movement disorders), autonomic dysfunction, treatment resistance, associations of symptom onset with infections such as group A streptococcus, comorbid autoimmune diseases or malignancies. Clinical investigations may also reveal alterations such as increased levels of anti-basal ganglia or dopamine receptor antibodies or inflammatory changes in the basal ganglia in neuroimaging. Based on these red flag signs, the criteria for a possible, probable, and definite autoimmune OCD subtype are proposed.
  •  
9.
  • Endres, Dominique, et al. (författare)
  • Spectrum of Novel Anti-Central Nervous System Autoantibodies in the Cerebrospinal Fluid of 119 Patients With Schizophreniform and Affective Disorders
  • 2022
  • Ingår i: Biological Psychiatry. - : Elsevier. - 0006-3223 .- 1873-2402. ; 92:4, s. 261-274
  • Tidskriftsartikel (refereegranskat)abstract
    • BACKGROUND: Autoimmune psychosis may be caused by well-characterized anti-neuronal autoantibodies, such as those against the NMDA receptor. However, the presence of additional anti-central nervous system (CNS) autoantibodies in these patients has not been systematically assessed.METHODS: Serum and cerebrospinal fluid (CSF) from patients with schizophreniform and affective syndromes were analyzed for immunoglobulin G anti-CNS autoantibodies using tissue-based assays with indirect immunofluorescence on unfixed murine brain tissue as part of an extended routine clinical practice. After an initial assessment of patients with red flags for autoimmune psychosis (n = 30), tissue-based testing was extended to a routine procedure (n = 89).RESULTS: Based on the findings from all 119 patients, anti-CNS immunoglobulin G autoantibodies against brain tissue were detected in 18% (n = 22) of patients (serum 9%, CSF 18%) following five principal patterns: 1) against vascular structures, most likely endothelial cells (serum 3%, CSF 8%); 2) against granule cells in the cerebellum and/or hippocampus (serum 4%, CSF 6%); 3) against myelinated fibers (serum 2%, CSF 2%); 4) against cerebellar Purkinje cells (serum 0%, CSF 2%); and 5) against astrocytes (serum 1%, CSF 1%). The patients with novel anti-CNS autoantibodies showed increased albumin quotients (p =.026) and white matter changes (p =.020) more frequently than those who tested negative for autoantibodies.CONCLUSIONS: The study demonstrates five novel autoantibody-binding patterns on brain tissue of patients with schizophreniform and affective syndromes. CSF yielded positive findings more frequently than serum analysis. The frequency and spectrum of autoantibodies in these patient groups may be broader than previously thought.
  •  
10.
  • Forouzanfar, Mohammad H, et al. (författare)
  • Global, regional, and national comparative risk assessment of 79 behavioural, environmental and occupational, and metabolic risks or clusters of risks in 188 countries, 1990-2013 : a systematic analysis for the Global Burden of Disease Study 2013.
  • 2015
  • Ingår i: The Lancet. - 0140-6736 .- 1474-547X. ; 386:10010, s. 2287-2323
  • Tidskriftsartikel (refereegranskat)abstract
    • BACKGROUND: The Global Burden of Disease, Injuries, and Risk Factor study 2013 (GBD 2013) is the first of a series of annual updates of the GBD. Risk factor quantification, particularly of modifiable risk factors, can help to identify emerging threats to population health and opportunities for prevention. The GBD 2013 provides a timely opportunity to update the comparative risk assessment with new data for exposure, relative risks, and evidence on the appropriate counterfactual risk distribution.METHODS: Attributable deaths, years of life lost, years lived with disability, and disability-adjusted life-years (DALYs) have been estimated for 79 risks or clusters of risks using the GBD 2010 methods. Risk-outcome pairs meeting explicit evidence criteria were assessed for 188 countries for the period 1990-2013 by age and sex using three inputs: risk exposure, relative risks, and the theoretical minimum risk exposure level (TMREL). Risks are organised into a hierarchy with blocks of behavioural, environmental and occupational, and metabolic risks at the first level of the hierarchy. The next level in the hierarchy includes nine clusters of related risks and two individual risks, with more detail provided at levels 3 and 4 of the hierarchy. Compared with GBD 2010, six new risk factors have been added: handwashing practices, occupational exposure to trichloroethylene, childhood wasting, childhood stunting, unsafe sex, and low glomerular filtration rate. For most risks, data for exposure were synthesised with a Bayesian meta-regression method, DisMod-MR 2.0, or spatial-temporal Gaussian process regression. Relative risks were based on meta-regressions of published cohort and intervention studies. Attributable burden for clusters of risks and all risks combined took into account evidence on the mediation of some risks such as high body-mass index (BMI) through other risks such as high systolic blood pressure and high cholesterol.FINDINGS: All risks combined account for 57·2% (95% uncertainty interval [UI] 55·8-58·5) of deaths and 41·6% (40·1-43·0) of DALYs. Risks quantified account for 87·9% (86·5-89·3) of cardiovascular disease DALYs, ranging to a low of 0% for neonatal disorders and neglected tropical diseases and malaria. In terms of global DALYs in 2013, six risks or clusters of risks each caused more than 5% of DALYs: dietary risks accounting for 11·3 million deaths and 241·4 million DALYs, high systolic blood pressure for 10·4 million deaths and 208·1 million DALYs, child and maternal malnutrition for 1·7 million deaths and 176·9 million DALYs, tobacco smoke for 6·1 million deaths and 143·5 million DALYs, air pollution for 5·5 million deaths and 141·5 million DALYs, and high BMI for 4·4 million deaths and 134·0 million DALYs. Risk factor patterns vary across regions and countries and with time. In sub-Saharan Africa, the leading risk factors are child and maternal malnutrition, unsafe sex, and unsafe water, sanitation, and handwashing. In women, in nearly all countries in the Americas, north Africa, and the Middle East, and in many other high-income countries, high BMI is the leading risk factor, with high systolic blood pressure as the leading risk in most of Central and Eastern Europe and south and east Asia. For men, high systolic blood pressure or tobacco use are the leading risks in nearly all high-income countries, in north Africa and the Middle East, Europe, and Asia. For men and women, unsafe sex is the leading risk in a corridor from Kenya to South Africa.INTERPRETATION: Behavioural, environmental and occupational, and metabolic risks can explain half of global mortality and more than one-third of global DALYs providing many opportunities for prevention. Of the larger risks, the attributable burden of high BMI has increased in the past 23 years. In view of the prominence of behavioural risk factors, behavioural and social science research on interventions for these risks should be strengthened. Many prevention and primary care policy options are available now to act on key risks.FUNDING: Bill & Melinda Gates Foundation.
  •  
11.
  • Hudson, Lawrence N, et al. (författare)
  • The database of the PREDICTS (Projecting Responses of Ecological Diversity In Changing Terrestrial Systems) project
  • 2017
  • Ingår i: Ecology and Evolution. - : John Wiley & Sons. - 2045-7758. ; 7:1, s. 145-188
  • Tidskriftsartikel (refereegranskat)abstract
    • The PREDICTS project-Projecting Responses of Ecological Diversity In Changing Terrestrial Systems (www.predicts.org.uk)-has collated from published studies a large, reasonably representative database of comparable samples of biodiversity from multiple sites that differ in the nature or intensity of human impacts relating to land use. We have used this evidence base to develop global and regional statistical models of how local biodiversity responds to these measures. We describe and make freely available this 2016 release of the database, containing more than 3.2 million records sampled at over 26,000 locations and representing over 47,000 species. We outline how the database can help in answering a range of questions in ecology and conservation biology. To our knowledge, this is the largest and most geographically and taxonomically representative database of spatial comparisons of biodiversity that has been collated to date; it will be useful to researchers and international efforts wishing to model and understand the global status of biodiversity.
  •  
12.
  • Murray, Christopher J. L., et al. (författare)
  • Population and fertility by age and sex for 195 countries and territories, 1950–2017: a systematic analysis for the Global Burden of Disease Study 2017
  • 2018
  • Ingår i: The Lancet. - 1474-547X .- 0140-6736. ; 392:10159, s. 1995-2051
  • Tidskriftsartikel (refereegranskat)abstract
    • Background: Population estimates underpin demographic and epidemiological research and are used to track progress on numerous international indicators of health and development. To date, internationally available estimates of population and fertility, although useful, have not been produced with transparent and replicable methods and do not use standardised estimates of mortality. We present single-calendar year and single-year of age estimates of fertility and population by sex with standardised and replicable methods. Methods: We estimated population in 195 locations by single year of age and single calendar year from 1950 to 2017 with standardised and replicable methods. We based the estimates on the demographic balancing equation, with inputs of fertility, mortality, population, and migration data. Fertility data came from 7817 location-years of vital registration data, 429 surveys reporting complete birth histories, and 977 surveys and censuses reporting summary birth histories. We estimated age-specific fertility rates (ASFRs; the annual number of livebirths to women of a specified age group per 1000 women in that age group) by use of spatiotemporal Gaussian process regression and used the ASFRs to estimate total fertility rates (TFRs; the average number of children a woman would bear if she survived through the end of the reproductive age span [age 10–54 years] and experienced at each age a particular set of ASFRs observed in the year of interest). Because of sparse data, fertility at ages 10–14 years and 50–54 years was estimated from data on fertility in women aged 15–19 years and 45–49 years, through use of linear regression. Age-specific mortality data came from the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2017 estimates. Data on population came from 1257 censuses and 761 population registry location-years and were adjusted for underenumeration and age misreporting with standard demographic methods. Migration was estimated with the GBD Bayesian demographic balancing model, after incorporating information about refugee migration into the model prior. Final population estimates used the cohort-component method of population projection, with inputs of fertility, mortality, and migration data. Population uncertainty was estimated by use of out-of-sample predictive validity testing. With these data, we estimated the trends in population by age and sex and in fertility by age between 1950 and 2017 in 195 countries and territories. Findings: From 1950 to 2017, TFRs decreased by 49·4% (95% uncertainty interval [UI] 46·4–52·0). The TFR decreased from 4·7 livebirths (4·5–4·9) to 2·4 livebirths (2·2–2·5), and the ASFR of mothers aged 10–19 years decreased from 37 livebirths (34–40) to 22 livebirths (19–24) per 1000 women. Despite reductions in the TFR, the global population has been increasing by an average of 83·8 million people per year since 1985. The global population increased by 197·2% (193·3–200·8) since 1950, from 2·6 billion (2·5–2·6) to 7·6 billion (7·4–7·9) people in 2017; much of this increase was in the proportion of the global population in south Asia and sub-Saharan Africa. The global annual rate of population growth increased between 1950 and 1964, when it peaked at 2·0%; this rate then remained nearly constant until 1970 and then decreased to 1·1% in 2017. Population growth rates in the southeast Asia, east Asia, and Oceania GBD super-region decreased from 2·5% in 1963 to 0·7% in 2017, whereas in sub-Saharan Africa, population growth rates were almost at the highest reported levels ever in 2017, when they were at 2·7%. The global average age increased from 26·6 years in 1950 to 32·1 years in 2017, and the proportion of the population that is of working age (age 15–64 years) increased from 59·9% to 65·3%. At the national level, the TFR decreased in all countries and territories between 1950 and 2017; in 2017, TFRs ranged from a low of 1·0 livebirths (95% UI 0·9–1·2) in Cyprus to a high of 7·1 livebirths (6·8–7·4) in Niger. The TFR under age 25 years (TFU25; number of livebirths expected by age 25 years for a hypothetical woman who survived the age group and was exposed to current ASFRs) in 2017 ranged from 0·08 livebirths (0·07–0·09) in South Korea to 2·4 livebirths (2·2–2·6) in Niger, and the TFR over age 30 years (TFO30; number of livebirths expected for a hypothetical woman ageing from 30 to 54 years who survived the age group and was exposed to current ASFRs) ranged from a low of 0·3 livebirths (0·3–0·4) in Puerto Rico to a high of 3·1 livebirths (3·0–3·2) in Niger. TFO30 was higher than TFU25 in 145 countries and territories in 2017. 33 countries had a negative population growth rate from 2010 to 2017, most of which were located in central, eastern, and western Europe, whereas population growth rates of more than 2·0% were seen in 33 of 46 countries in sub-Saharan Africa. In 2017, less than 65% of the national population was of working age in 12 of 34 high-income countries, and less than 50% of the national population was of working age in Mali, Chad, and Niger. Interpretation: Population trends create demographic dividends and headwinds (ie, economic benefits and detriments) that affect national economies and determine national planning needs. Although TFRs are decreasing, the global population continues to grow as mortality declines, with diverse patterns at the national level and across age groups. To our knowledge, this is the first study to provide transparent and replicable estimates of population and fertility, which can be used to inform decision making and to monitor progress. Funding: Bill & Melinda Gates Foundation.
  •  
13.
  • Shu, Xiang, et al. (författare)
  • Associations of obesity and circulating insulin and glucose with breast cancer risk : a Mendelian randomization analysis
  • 2019
  • Ingår i: International Journal of Epidemiology. - : OXFORD UNIV PRESS. - 0300-5771 .- 1464-3685. ; 48:3, s. 795-806
  • Tidskriftsartikel (refereegranskat)abstract
    • Background: In addition to the established association between general obesity and breast cancer risk, central obesity and circulating fasting insulin and glucose have been linked to the development of this common malignancy. Findings from previous studies, however, have been inconsistent, and the nature of the associations is unclear. Methods: We conducted Mendelian randomization analyses to evaluate the association of breast cancer risk, using genetic instruments, with fasting insulin, fasting glucose, 2-h glucose, body mass index (BMI) and BMI-adjusted waist-hip-ratio (WHRadj BMI). We first confirmed the association of these instruments with type 2 diabetes risk in a large diabetes genome-wide association study consortium. We then investigated their associations with breast cancer risk using individual-level data obtained from 98 842 cases and 83 464 controls of European descent in the Breast Cancer Association Consortium. Results: All sets of instruments were associated with risk of type 2 diabetes. Associations with breast cancer risk were found for genetically predicted fasting insulin [odds ratio (OR) = 1.71 per standard deviation (SD) increase, 95% confidence interval (CI) = 1.26-2.31, p = 5.09 x 10(-4)], 2-h glucose (OR = 1.80 per SD increase, 95% CI = 1.3 0-2.49, p = 4.02 x 10(-4)), BMI (OR = 0.70 per 5-unit increase, 95% CI = 0.65-0.76, p = 5.05 x 10(-19)) and WHRadj BMI (OR = 0.85, 95% CI = 0.79-0.91, p = 9.22 x 10(-6)). Stratified analyses showed that genetically predicted fasting insulin was more closely related to risk of estrogen-receptor [ER]-positive cancer, whereas the associations with instruments of 2h glucose, BMI and WHRadj BMI were consistent regardless of age, menopausal status, estrogen receptor status and family history of breast cancer. Conclusions: We confirmed the previously reported inverse association of genetically predicted BMI with breast cancer risk, and showed a positive association of genetically predicted fasting insulin and 2-h glucose and an inverse association of WHRadj BMI with breast cancer risk. Our study suggests that genetically determined obesity and glucose/insulin-related traits have an important role in the aetiology of breast cancer.
  •  
14.
  •  
15.
  •  
16.
  • Abbafati, Cristiana, et al. (författare)
  • 2020
  • Tidskriftsartikel (refereegranskat)
  •  
Skapa referenser, mejla, bekava och länka
  • Resultat 1-16 av 16
Typ av publikation
tidskriftsartikel (11)
konferensbidrag (4)
forskningsöversikt (1)
Typ av innehåll
refereegranskat (16)
Författare/redaktör
Cunningham, Miriam (6)
Brenner, Hermann (5)
Cunningham, Paul (5)
Ekenberg, Love (4)
Bernabe, Eduardo (3)
Esteghamati, Alireza (3)
visa fler...
Farzadfar, Farshad (3)
Kimokoti, Ruth W. (3)
Kumar, G. Anil (3)
Lotufo, Paulo A. (3)
Mendoza, Walter (3)
Pereira, David M. (3)
Werdecker, Andrea (3)
Xu, Gelin (3)
Estep, Kara (3)
Moradi-Lakeh, Maziar (3)
Bennett, Derrick A. (3)
Eshrati, Babak (3)
Kim, Daniel (3)
Kosen, Soewarta (3)
Pourmalek, Farshad (3)
Shiri, Rahman (3)
Tonelli, Marcello (3)
Yano, Yuichiro (3)
Allebeck, Peter (3)
Sliwa, Karen (3)
Norrving, Bo (3)
Bell, Michelle L (3)
Shibuya, Kenji (3)
Fereshtehnejad, Seye ... (3)
Gamkrelidze, Amiran (3)
De Leo, Diego (3)
Hsairi, Mohamed (3)
Seedat, Soraya (3)
Tabb, Karen M (3)
Cirillo, Massimo (3)
Remuzzi, Giuseppe (3)
Dokova, Klara (3)
Giussani, Giorgia (3)
Cardenas, Rosario (3)
Hu, Guoqing (3)
Karch, Andre (3)
Nangia, Vinay (3)
Oh, In-Hwan (3)
Sahraian, Mohammad A ... (3)
Schwebel, David C. (3)
Sykes, Bryan L. (3)
Bikbov, Boris (3)
Alla, François (3)
Barrero, Lope H (3)
visa färre...
Lärosäte
Stockholms universitet (7)
Uppsala universitet (6)
Lunds universitet (6)
Karolinska Institutet (6)
Högskolan Dalarna (3)
Umeå universitet (2)
visa fler...
Linnéuniversitetet (2)
Sveriges Lantbruksuniversitet (2)
Göteborgs universitet (1)
Mittuniversitetet (1)
Chalmers tekniska högskola (1)
visa färre...
Språk
Engelska (16)
Forskningsämne (UKÄ/SCB)
Naturvetenskap (7)
Medicin och hälsovetenskap (7)
Samhällsvetenskap (2)
Teknik (1)

År

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Stäng

Kopiera och spara länken för att återkomma till aktuell vy