Academic literature on the topic 'Church of England Institute (N.S.)'

Abstract In the 1850's John Harden and E.A. Watkins, missionaries of the Church Missionary Society (CMS) to James Bay, began the work of adapting James Evan's Cree syllabic orthography to Inuktitut. Watkins' introduced the syllabic writing system to Inuit at Fort George and Little Whale River in 1855, and that same year Harden printed a small book of scripture verses in syllables on his press at Moose Factory. In 1865, at the request of CMS Secretary Henry Venn, Harden and Watkins met in conference in England and modified the syllabic system to allow a more precise rendering of both Inuktitut and Moose Cree. It remained for Edmund James Peck, who arrived in the diocese in 1876, to devote his attention to the translation of scripture into Inuktitut in Harden and Watkins' orthography. Only minor changes were made in the Inuktitut orthography until the major revision under the direction of the Inuit Cultural Institute in the 1970's.

Subject of this article is the copy of Four Gospels preserved at the Church Institute in Sofia (gr. 949), which was displayed in the Brilliance of Byzantium Exhibition organized during the 22nd International Congress of Byzantine Studies (August 22 - 27, 2011) and which we assumed to have been produced by the hand of one of the most famous scribes at the end of the 13th and the beginning of the 14th century, i.e. Theodore Hagiopetrites. The type of the script employed in the Four Gospels at the Church Institute (CHAI gr. 949) is in the so-called by L. Politis unique ?Hagiopetrites Style?. Although the manuscript does not contain a colophon, comparison to the manuscripts of Theodore Hagiopetrites known to us and especially to Cod. D. gr. 29 (Olim. Kos. 35) at the Ivan Dujcev Centre - an autograph of the scribe of 1307, as well as to another manuscript from Saint Petersburg, Cod. gr. of ASUSSR, No 10/667 of the 14th century, provides good reasons to assume that the Four Gospels manuscript (CHAI gr. 949) was also produced by Theodore Hagiopetrites. Our certainty was further substantiated after we had studied in situ the Four Gospels from Academician N. P. Likhachev?s archive published by Igor Medvedev in the collection ? In Memoriam Ivan Dujcev? of 1988 which is currently kept under No 10/667 in the Archive of the Leningrad Section of the Institute of History at the Russian Academy of Science. Having compared the illumination and the specifics of motif stylization, as well as the specific colouring, we could assert that the two manuscripts manifest pronounced similarities. Thereby, the 27 manuscripts by T. Hagiopetrites published by R. Nelson should also be supplemented by the Four Gospels at the Church Institute (CHAI gr. 949) in addition to the Apostle Lectionary of 1307, autograph of Theodore Hagiopetrites at the Dujcev Centre, Cod. D. gr. 29 (Olim. Kos. 35), which R. Nelson briefly mentioned in his preface, and the Saint Petersburg Four Gospels, published by I. Medvedev.

Readers are invited to contact Greg S. Loeben in writing at Midwestern University, Glendale Campus, Bioethics Program, 19555 N. 59th Ave., Glendale, AZ 85308 (gloebe@midwestern.edu) regarding books they would like to see reviewed or books they are interested in reviewing.

Abstract Objective To develop an app for Android smartphones (named 3Ollin) that assess the fall risk through the automated analysis of three physical performance (PP) tests and the history of falls of the participant. Design Cross-sectional design. Setting Community-dwelling older adults studied at the Functional Evaluation Laboratory at the National Institute of Geriatrics in Mexico. Participants Older adults (n=223) living in Mexico City were included. The participants were recruited from groups of pensioners from the National Autonomous University of Mexico, church groups, and other community programs. Measurements Data were collected about demographics, comorbidities, cognitive status, nutritional status, dependency and PP variables. The 3Ollin app evaluates the PP of the participants through the history of falls, the Timed Up and Go, the 30-second chair stand, and the 4-stage balance tests. The app incorporates them into the CDC’s Algorithm for Fall Risk Screening, Assessment, and Intervention. Methods All participants were evaluated by trained staff. The app has a registration system for users and patients, allows to perform the PP tests, acquires the data from the sensors signals, and sends and stores the information in the server of the National Institute of Geriatrics in Mexico. Results The mean age of the studied population was 73.5±7.0 years, 77.6% were women, and 37.2% did not complete the 4-stage balance test. The mean percentage error (MPE) between the gait speed measured through the GAITRite walkway (ms=103.5±26.1 cm/s) and the 3Ollin app (ms=100.0±30.3 cm/s) was 10.7%. The MPE between the number of chair lifts in 30 s according to the evaluator's observations (mCL=15±6 repetitions), and the 3Ollin app (mCL=19±6 repetitions) was 23.4%. Additionally, 87% were correctly classified according to the 3Ollin app. Conclusions This design first step of the 3Ollin app probed to offer a valid, efficient, costless performance evaluation, without the need of a laboratory environment.

Objectives: The aim of this study was to identify and critically appraise the use of Value of Information (VOI) analyses undertaken as part of health technology assessment (HTA) reports in England and Wales.Methods: A systematic review of National Institute for Health Research (NIHR) funded HTA reports published between 2004 and 2013 identified the use of VOI methods and key analytical details in terms of: (i) types of VOI methodology used; (ii) parameters and key assumptions; and (iii) conclusions drawn in terms of the need for further research.Results: A total of 512 HTA reports were published during the relevant timeframe. Of these, 203 reported systematic review and economic modeling studies and 25 of these had used VOI method(s). Over half of the twenty-five studies (n = 13) conducted both EVPI (Expected Value of Perfect Information) and EVPPI (Expected Value of Partial Perfect Information) analyses. Eight studies conducted EVPI analysis, three studies conducted EVPI, EVPPI, and EVSI (Expected Value of Sampling Information) analyses and one study conducted EVSI analysis only. The level of detail reporting the methods used to conduct the VOI analyses varied.Conclusions: This review has shown that the frequency of the use of VOI methods is increasing at a slower pace compared with the published volume of HTA reports. This review also suggests that analysts reporting VOI method(s) in HTA reports should aim to describe the method(s) in sufficient detail to enable and encourage decision-makers guiding research prioritization decisions to use the potentially valuable outputs from quantitative VOI analyses.

Review of European Studies wishes to acknowledge the following individuals for their assistance with peer review of manuscripts for this issue. Their help and contributions in maintaining the quality of the journal are greatly appreciated. Review of European Studies is recruiting reviewers for the journal. If you are interested in becoming a reviewer, we welcome you to join us. Please find the application form and details at http://recruitment.ccsenet.org and e-mail the completed application form to res@ccsenet.org. Reviewers for Volume 11, Number 2 Alex Almici, Università degli Studi di Brescia, Italy Ana Souto, Nottingham Trent University, UK Anna Cebotari, Academy of Economic Studies of Moldova, Republica Moldova Bing Hiong Ngu, The University of New England, Australia Carmen Ramos, University of Oviedo, Spain Dave Williams, Dublin Institute of Technology, Ireland Edwards, Beverly L, Fayetteville State University Department of Social Work, United States Emilio Greco, "Sapienza" University of Rome, Italy Gabriela Gruber, Lucian Blaga University of Sibiu, Romania George Mathew Nalliveettil, Aljouf University, Saudi Arabia George Touche, Texas A&M University, USA Katja Eman, University of Maribor, Slovenia Lena Arampatzidou, Aristotle University Of Thessaloniki, Greece Maheran Zakaria, Universiti Teknologi MARA, Malaysia Maria Pescaru, University of Pitești, ROMANIA Meenal Tula, University of Hyderabad, India Nasina Md, Universiti Sains Malaysia, Malaysia Natalija Vrecer, Slovenian Institute for Adult Education (SIAE), Slovenia Nunzia Di Cristo Bertali, Liverpool John Moores University, United Kingdom Patrick van Esch, Moravian College, Australia & US Sara Núñez Izquierdo, University of Salamanca, Spain Savanam Chandra Sekhar, St. Ann’s College of Engineering & Technology, Chirala, India Skaidrė Žičkienė, Šiauliai University, Lithuania Tryfon Korontzis, Hellenic National School of Local Government , Greece Vicenta Gisbert, Universidad de La Laguna, Spain

Parthenium (Parthenium hysterophorus L.) has been a target of weed researchers in India for more than four decades. The weed is attacked by many pathogens, some of which have been tried as mycoherbicides with mixed results (1). In an effort to identify more pathogens of parthenium, surveys were conducted in different regions. A typical foliar disease was frequently observed in several districts of Karnataka State, especially during the winter months of 1996 to 1998. The primary symptoms were circular to irregular, light brown to gray leaf spots, ranging from 2 to 8 mm in diameter. Careful observation of diseased plants revealed that the development of several lesions in close proximity resulted in a rapid necrosis and withering of the entire leaf. The suspected causal organism, which was a dark, chocolate-brown fungus, grew well on potato-dextrose agar at 25°C and a 12-h photoperiod. It produced slowly maturing conidia (20 to 27 × 12 to 14 μm), which were dark brown, ellipsoid, thick-walled, and single-septate with longitudinal striations. A dense conidial suspension (108 conidia per ml) of the fungus was evenly applied (250 μl per leaf) on detached, surface-sterilized, healthy parthenium leaves (N = 10), and infection was ascertained after 4 days of incubation at 26 ± 2°C in petri dishes lined with moist cotton. When 45-day-old pot-grown parthenium plants (N = 50) were similarly inoculated and maintained above 95% RH for at least 48 h, typical symptoms resembling those of naturally infected plants were visible on 88% of the plants within 3 weeks of incubation at 28 ± 2°C. Whereas the fungus was consistently isolated from diseased leaves of inoculated plants, with 80% frequency of reisolation, uninoculated controls neither displayed symptoms nor yielded the pathogen. The experiment was performed three times with similar results, satisfying Koch's postulates. The identity of one of the virulent isolates, WF(Ph)8 (ex Siddeswaranadurga, Chitradurga district, December 1997), was confirmed as Lasiodiplodia theobromae (Pat.) Griffon. & Maubl. (=Botryodiplodia theobromae Pat.) (IMI 378919a) at CABI Bioscience, UK Centre (Egham). Although it is a ubiquitous tropical and subtropical plant pathogen that occurs between 40°N and 40°S (2), it was not previously recorded as a cause of leaf disease on parthenium. Investigations on the possible use of the pathogen as a mycoherbicide have given encouraging results. References: (1) P. Sreerama Kumar. 1998. Pages 192-210 in: Biological Suppression of Plant Diseases, Phytoparasitic Nematodes and Weeds. S. P. Singh and S. S. Hussaini, eds. Project Directorate of Biological Control, Bangalore, India. (2) B. C. Sutton. 1980. The Coelomycetes. Commonwealth Mycological Institute, Kew, England.

Background The number of people living with dementia is greater than the number with a diagnosis of dementia recorded in primary care. This suggests that a significant number are living with dementia that is undiagnosed. Little is known about this group and there is little quantitative evidence regarding the consequences of diagnosis for people with dementia. Objectives The aims of this study were to (1) describe the population meeting the criteria for dementia but without diagnosis, (2) identify predictors of being diagnosed and (3) estimate the effect of diagnosis on mortality, move to residential care, social participation and well-being. Design A record linkage study of a subsample of participants (n = 598) from the Cognitive Function and Ageing Study II (CFAS II) (n = 7796), an existing cohort study of the population of England aged ≥ 65 years, with standardised validated assessment of dementia and consent to access medical records. Data sources Data on dementia diagnoses from each participant’s primary care record and covariate and outcome data from CFAS II. Setting A population-representative cohort of people aged ≥ 65 years from three regions of England between 2008 and 2011. Participants A total of 598 CFAS II participants, which included all those with dementia who consented to medical record linkage (n = 449) and a stratified sample without dementia (n = 149). Main outcome measures The main outcome was presence of a diagnosis of dementia in each participant’s primary care record at the time of their CFAS II assessment(s). Other outcomes were date of death, cognitive performance scores, move to residential care, hospital stays and social participation. Results Among people with dementia, the proportion with a diagnosis in primary care was 34% in 2008–11 and 44% in 2011–13. In both periods, a further 21% had a record of a concern or a referral but no diagnosis. The likelihood of having a recorded diagnosis increased with severity of impairment in memory and orientation, but not with other cognitive impairment. In multivariable analysis, those aged ≥ 90 years and those aged < 70 years were less likely to be diagnosed than other age groups; those living with a spouse (odds ratio 2.38, 95% confidence interval 1.04 to 5.41) were more likely to be diagnosed than people living alone. The median time to diagnosis from first meeting the criteria for dementia was 3 years. Diagnosis did not affect survival or the probability of a move to residential care. Limitations People with moderate to severe dementia at baseline could not consent to record linkage. The small numbers in some groups limited power to detect effects. Conclusions The lack of relationship between severity of non-memory impairment and diagnosis may reflect low awareness of other symptoms of dementia. There remains little objective evidence for benefits of diagnosis for people with dementia. Future work Potential benefits of diagnosis can be realised only if effective interventions are accessible to patients and carers. Future work should focus on improving support for people living with cognitive impairment. Study registration National Institute for Health Research Clinical Research Network Central Portfolio Management System (CPMS 30655). Funding This project was funded by the National Institute for Health Research (NIHR) Health Services and Delivery Research programme and will be published in full in Health Services and Delivery Research; Vol. 8, No. 20. See the NIHR Journals Library website for further project information.

BackgroundConcerns about fragmented community mental health care have led to the development of the care programme approach in England and care and treatment planning in Wales. These systems require those people receiving mental health services to have a care co-ordinator, a written care plan and regular reviews of their care. Care planning and co-ordination should be recovery-focused and personalised, with people taking more control over their own support and treatment.Objective(s)We aimed to obtain the views and experiences of various stakeholders involved in community mental health care; to identify factors that facilitated, or acted as barriers to, personalised, collaborative and recovery-focused care planning and co-ordination; and to make suggestions for future research.DesignA cross-national comparative mixed-methods study involving six NHS sites in England and Wales, including a meta-narrative synthesis of relevant policies and literature; a survey of recovery, empowerment and therapeutic relationships in service users (n = 449) and recovery in care co-ordinators (n = 201); embedded case studies involving interviews with service providers, service users and carers (n = 117); and a review of care plans (n = 33).Review methodsA meta-narrative mapping method.ResultsQuantitative and qualitative data were analysed within and across sites using inferential statistics, correlations and the framework method. Our study found significant differences for scores on therapeutic relationships related to positive collaboration and clinician input. We also found significant differences between sites on recovery scores for care co-ordinators related to diversity of treatment options and life goals. This suggests that perceptions relating to how recovery-focused care planning works in practice are variable across sites. Interviews found great variance in the experiences of care planning and the understanding of recovery and personalisation within and across sites, with some differences between England and Wales. Care plans were seen as largely irrelevant by service users, who rarely consulted them. Care co-ordinators saw them as both useful records and also an inflexible administrative burden that restricted time with service users. Service users valued their relationships with care co-ordinators and saw this as being central to their recovery. Carers reported varying levels of involvement in care planning. Risk was a significant concern for workers but this appeared to be rarely discussed with service users, who were often unaware of the content of risk assessments.LimitationsLimitations include a relatively low response rate of between 9% and 19% for the survey and a moderate level of missing data on one measure. For the interviews, there may have been an element of self-selection or inherent biases that were not immediately apparent to the researchers.ConclusionsThe administrative elements of care co-ordination reduce opportunities for recovery-focused and personalised work. There were few shared understandings of recovery, which may limit shared goals. Conversations on risk appeared to be neglected and assessments kept from service users. A reluctance to engage in dialogue about risk management may work against opportunities for positive risk-taking as part of recovery-focused work.Future workResearch should be commissioned to investigate innovative approaches to maximising staff contact time with service users and carers; enabling shared decision-making in risk assessments; and promoting training designed to enable personalised, recovery-focused care co-ordination.FundingThe National Institute for Health Research Health Services and Delivery Research programme.