Academic literature on the topic 'Campbell Committee'

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Journal articles on the topic "Campbell Committee"

1

Berg, Chris. "The Campbell Committee and the origins of ‘deregulation’ in Australia." Australian Journal of Political Science 51, no. 4 (August 23, 2016): 711–26. http://dx.doi.org/10.1080/10361146.2016.1219315.

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Rollin, Henry R. "The Red Handbook: an historic centenary." Bulletin of the Royal College of Psychiatrists 10, no. 10 (October 1986): 279. http://dx.doi.org/10.1192/s0140078900023117.

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On 21 February 1884, a sub-committee of the Medico-Psychological Association meeting in Glasgow was appointed to prepare a handbook ‘in the hope of helping Attendants on the insane to a due understanding of the work in which they are engaged’. With commendable speed the four gentlemen concerned, Drs A. Campbell Clark, C. McIvor Campbell, A. R. Turnbull and A. R. Urquart, completed their allotted task, and in 1885 The Handbook For The Instruction Of Attendants On The Insane was published.
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3

Moore, P. G. "The West of Scotland Regional Dredging Committee of the BAAS: Firth of Clyde dredging activities and participants’ circumstances impinging thereon (1834–1856)." Archives of Natural History 37, no. 1 (April 2010): 39–57. http://dx.doi.org/10.3366/e0260954109001648.

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Insights gained into the activities of the West of Scotland Regional Dredging Committee of the British Association for the Advancement of Science (BAAS): a committee comprising the Reverend Dr Charles Popham Miles (Chairman), Dr Robert Kaye Greville, Professor John Hutton Balfour and Thomas Campbell Eyton, are presented. Based particularly on previously unreported correspondence between Miles and Balfour, and between Greville and Balfour that is housed in the archives of the Royal Botanic Garden Edinburgh, the backgrounds of these persons (like their shared religious leanings) are illuminated and their practical experiences of dredging in the Firth of Clyde, notably in Lamlash Bay (Isle of Arran), brought into focus. Economic aspects relating to the costs of dredging, the finances of participants and the adequacy of the initial BAAS grant are highlighted and other social aspects commented upon. There is no known surviving contemporary account of the interactions between this network of BAAS dredging committee members, so this correspondence seemingly remains, to date, the only information that is available as primary sources.
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Maurer, Christian. "Archibald Campbell and the Committee for Purity of Doctrine on Natural Reason, Natural Religion, and Revelation." History of European Ideas 42, no. 2 (February 23, 2015): 256–75. http://dx.doi.org/10.1080/01916599.2014.1002969.

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Pinceratto, E. J. "THE MINERVA GAS FIELD EIA—A CASE STUDY OF COMMUNITY INVOLVEMENT IN DECISIONMAKING." APPEA Journal 41, no. 1 (2001): 767. http://dx.doi.org/10.1071/aj00045.

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The Minerva gas field is situated approximately 10 km offshore Port Campbell, Victoria, in the Southern Ocean in water depth of approximately 60 m. The development involves the drilling and completion of two wells, offshore pipelines to the coast, subterranean shore crossing and onshore pipelines to a gas treatment plant where liquids will be removed prior to exporting the gas.From the outset, the project attracted the interest of the local and wider community due to its proximity to the highly regarded Port Campbell National Park. The National Park is known for its unique geomorphological features, its fauna and flora and aboriginal heritage sites.The development has been subject to a dual jurisdiction, State and Federal, Environmental Impact Assessment (EIA) process. The process included the formation of a Community Consultative Committee consisting of representatives from government agencies, local community groups, environmental groups, industry associations and the proponent. The Committee provided input to the scope of the EIA and reviewed and endorsed the studies and report prior to public exhibition. An independent panel hearing and ministerial assessments followed public exhibition.A phased process was adopted in the selection of routes, sites and technologies to achieve the lowest practicable environmental impact. Each phase was supported by studies of environmental aspects, fauna, flora, heritage, visual and social impacts. The process commenced on a regional scale and progressively refined the concept and the study area. Detailed studies of key environmental aspects were conducted for the selected development options.The final development concept addressed the key findings of the baseline and subsequent environmental studies and was largely supported by an independent panel. However, there still remained concerns by sectors of the community on the issue of precedent and integrity of the National Park. The Ministerial assessment reflected the issues of community value above technical, environmental, archaeological and heritage considerations.
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Van Dulmen, Sandra, and Juan Mezzich. "Summary Report of the Ninth Geneva Conference on Person Centered Medicine." International Journal of Person Centered Medicine 6, no. 2 (July 13, 2016): 126–30. http://dx.doi.org/10.5750/ijpcm.v6i2.581.

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For the 9th time, the International College for Person-Centered Medicine (ICPCM) held its annual conference on Person-Centered Medicine in Geneva, Switzerland. Like previous years, the conference was formally co-sponsored by the World Health Organization, the World Medical Association, the World Organization of Family Doctors, the International Council of Nurses, the International Alliance of Patients' Organizations and thirty other global health professional and academic institutions. The organizing committee was composed of the ICPCM Board members, Ruth Wilson as program director and Islene Araujo de Carvalho, Jim Campbell and Nuria Toro Polanco from WHO. Material support was provided by the World Medical Association, the World Health Organization, the Geneva University Hospital, and the Paul Tournier Association.
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Black, Amy, and Stephen Brooke. "The Labour Party, Women, and the Problem of Gender, 1951–1966." Journal of British Studies 36, no. 4 (October 1997): 419–52. http://dx.doi.org/10.1086/386144.

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Following the 1966 General Election, the Labour Party's Home Policy Committee observed that the party had, “for the first time, obtained a majority of the female vote” and remarked, “it would be very satisfactory if we could retain it.” Two years later, the Report of the Committee of Enquiry into Party Organisation emphasized the “imperative that the Party concerns itself with how to win much more support among women.” These comments not only betrayed a serious weakness in Labour's electoral support between 1951 and 1966 but also acknowledged an important lacuna in its broader political outlook.Given the party's electoral difficulties in the period after 1951, the first concern was particularly apposite. Beatrix Campbell, Nicky Hart, and Ina Zweiniger-Bargielowska have underlined the importance of this gender gap favoring the Conservatives after 1950 (see fig. 1). In the elections of 1951 and 1955, for example, Labour's vote among women lagged twelve and thirteen percentage points behind that of the Conservatives. Only in two elections between 1945 and 1970 did Labour enjoy leads among female voters, and these were much less substantial than those held by the Conservatives in 1951, 1955, 1959, and 1964. In rough numerical terms, this difference was potentially very significant. In 1951, for instance, women made up approximately 51.9 percent of the population of England, Scotland, and Wales and roughly 53.8 percent of those of voting age. With an electorate of 28.5 million, this meant a possible political advantage for the Conservatives of 1.2 million votes in an electoral contest where there were only .2 million votes between the two parties.
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8

Coogan, John W., and Peter F. Coogan. "The British Cabinet and the Anglo-French Staff Talks, 1905–1914: Who Knew What and When Did He Know It?" Journal of British Studies 24, no. 1 (January 1985): 110–31. http://dx.doi.org/10.1086/385827.

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The role of the British cabinet in the Anglo-French military conversations prior to the First World War has been and remains controversial. The acrimonious debate within the government during November 1911 seems linked inextricably to the flood of angry memoirs that followed August 1914 and to the continuing historical debate over the actions and motivations of the various ministers involved. Two generations of researchers now have examined an enormous body of evidence, yet the leading modern scholars continue to publish accounts that differ on the most basic questions. Historians have proved no more able than the ministers themselves were to reconcile the contradictory statements of honorable men. The persistence of these differences in historical literature demonstrates both the continuing confusion over the cabinet's role in the military conversations and the need for a renewed effort to resolve this confusion.The starting point for any discussion of the staff talks must be the recognition that the meaning of the term changed significantly over the nine years before the outbreak of World War I. The contacts began with a series of informal discussions between senior British and French officers during 1905. The first systematic conversations took place early in January 1906 under the authority of Lord Esher, a permanent member of the Committee of Imperial Defence (CID), and Sir George Clarke, the CID secretary. Later in that month a small group of ministers, including Prime Minister Sir Henry Campbell-Bannerman, sanctioned formal, ongoing exchanges between the two general staffs.
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9

Bejar, Rafael, Elli Papaemmanuil, Torsten Haferlach, Guillermo Garcia-Manero, Jaroslaw P. Maciejewski, Mikkael A. Sekeres, Matthew J. Walter, et al. "TP53 Mutation Status Divides MDS Patients with Complex Karyotypes into Distinct Prognostic Risk Groups: Analysis of Combined Datasets from the International Working Group for MDS-Molecular Prognosis Committee." Blood 124, no. 21 (December 6, 2014): 532. http://dx.doi.org/10.1182/blood.v124.21.532.532.

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Abstract Background: Complex karyotypes in patients with myelodysplastic syndromes (MDS) are defined by the presence of 3 or more cytogenetic abnormalities and are considered indicators of a poor prognosis by nearly all models in clinical use. There is evidence that the prognostic significance of complex karyotypes in MDS can be refined by considering the number of cytogenetic abnormalities or the presence of specific lesions, the presence of monosomy, and the mutation status of the TP53 gene. Mutations of TP53 are strongly associated with adverse clinical features including complex karyotypes, yet still have independent prognostic significance. Whether these mutations or other elements associated with complex karyotypes carry the greatest prognostic significance is unknown and has been the subject of recent contradictory findings. Here we examine the relationship between TP53 mutations, the number and type of chromosomal abnormalities, and clinical features including overall survival in a combined analysis of MDS patients with complex karyotypes. Methods: Data on 258 complex karyotype MDS patients from the US and Europe gathered by members of the International Working Group for Prognosis in MDS-Molecular Committee were combined for this analysis. Patients gave informed consent to have their data and clinical samples collected at their respective institutions in accordance with the Declaration of Helsinki. Tumor samples were examined for TP53 mutations primarily with next generation sequencing techniques. Categorical variables were compared using a Fisher exact test or Kruskal-Wallis test as appropriate, while continuous variables were compared using a Wilcoxon rank-sum test. All p-values reported are two-sided, unadjusted for multiple testing, and considered significant at the 0.05 level. Results: Of the 258 complex karyotype MDS samples examined, TP53 mutation status was determined in 223, of which 133 (60%) carried a TP53 mutation. Patients with TP53 mutations were slightly older than unmutated patients (median age 70.8 vs. 65.5 years, p=0.055), were more thrombocytopenic (median platelet count 42 vs. 78 x109/L, p=0.002), and had a greater percentage of bone marrow blasts (7.75% vs 4%, p=0.03). Mutated patients were also more likely to have a monosomal karyotype (85% vs. 59%, p<0.0001), have 5 or more chromosomal abnormalities (85% vs. 51%, p<0.0001), and have abnormalities of chromosome 17 (38% vs. 23%, p=0.03). Patients with TP53 mutation had a significantly shorter median overall survival of 7.7 months compared to 23.4 months for patients with unmutated TP53 (p<0.0001, see figure). Multivariate analysis that considered potential confounders such as monosomal karyotypes, number of abnormalities, blast proportions and platelet count identified TP53 mutation status as the most significant prognostic marker for overall survival (hazard ration [HR] 2.12, p<0.0001). The presence of only 3 or only 4 karyotype abnormalities was protective compared with 5 or more such lesions (HR 0.385, p=0.0005 for 3 lesions and HR 0.505, p=0.0083 for 4 lesions). Discussion: Despite strong associations with adverse clinical and cytogenetic abnormalities incorporated into existing prognostic scoring systems, TP53 mutations carry significant independent prognostic value for patients with MDS. In our multivariable analyses, TP53 mutation appears to dominate over monosomal karyotype as an adverse prognostic marker in MDS patients with complex cytogenetics. Many of the TP53 mutations identified had a small variant allele fraction suggesting that they were present in a disease subclone. The small number of mutant cells in these cases may be insufficient to alter clinical measures, but could still indicate a poor prognosis if they represent a clone capable of treatment resistance and rapid disease progression. This combined analysis is a work in progress that will include data from additional groups and explore mutation status of other MDS-related genes, TP53 variant allele fraction, clinical risk scores, and data from patients without complex karyotypes. Conclusions: Somatic TP53 mutations are highly enriched in MDS patients with complex karyotypes and identify a group with significantly shortened overall survival. Sequencing of TP53 can improve the prediction of prognosis in MDS patients with 3 or more chromosomal abnormalities. Figure 1 Figure 1. Disclosures Bejar: Genoptix Medical Laboratory: Consultancy, Honoraria, Licensed IP, no royalties Patents & Royalties, Membership on an entity's Board of Directors or advisory committees; Celgene: Membership on an entity's Board of Directors or advisory committees. Haferlach:MLL Munich Leukemia Laboratory: Other. Garcia-Manero:Celgene: Research Funding. Sekeres:Celgene: Membership on an entity's Board of Directors or advisory committees; Amgen Corp: Membership on an entity's Board of Directors or advisory committees; Boehringer-Ingelheim Corp: Membership on an entity's Board of Directors or advisory committees. Campbell:14M Genomics Limited: Consultancy, Equity Ownership.
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10

Bejar, Rafael, Elli Papaemmanuil, Torsten Haferlach, Guillermo Garcia-Manero, Jaroslaw P. Maciejewski, Mikkael A. Sekeres, Matthew J. Walter, et al. "Somatic Mutations in MDS Patients Are Associated with Clinical Features and Predict Prognosis Independent of the IPSS-R: Analysis of Combined Datasets from the International Working Group for Prognosis in MDS-Molecular Committee." Blood 126, no. 23 (December 3, 2015): 907. http://dx.doi.org/10.1182/blood.v126.23.907.907.

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Abstract Background Somatic mutations identified in patients with myelodysplastic syndromes (MDS) are associated with disease features and carry prognostic information independent of the International Prognostic Scoring System (IPSS) and the revised IPSS (IPSS-R). Risk models that include mutation information have been proposed, but not widely adopted. In practice, there is no consensus on how to best combine clinical information with tumor sequencing data to predict prognosis. To accomplish this, we must define the relevant genes to consider and accurately measure their prognostic impact. Here we examine the relationship between mutations in MDS-associated genes and clinically relevant measures, including overall survival, in a large, multi-center analysis of MDS patient cohorts collected around the globe. Methods Data on 3392 MDS patients gathered by members of the International Working Group for Prognosis in MDS-Molecular Committee were combined under the aegis of the MDS Foundation. Patients gave informed consent for collection of their data and tumor samples at their respective institutions in accordance with the Declaration of Helsinki. Samples were examined for somatic mutations primarily by next generation sequencing. Categorical variables were compared using a chi-squared test, while continuous variables were compared using a Wilcoxon rank-sum test. Overall survival (OS) was calculated from the date of the sequenced sample to the date of death and was censored at transplant or the last known follow-up time. P-values are two-sided and considered significant at the <0.001 level to adjust for multiple comparisons. Results Survival data were available for 3200 patients with a median follow up of 3.7 years and included 1671 deaths. Median survival of the cohort was 2.88 years. The 27 genes sequenced in at least half of the cohort and mutated in > 1.5% of samples were included for analysis (Figure 1). Mutations in 12 genes were strongly associated with shorter OS in univariate analyses (p<0.001 for each gene): ASXL1, CBL, EZH2, IDH2, NF1, NRAS, PTPN11, RUNX1, SRSF2, STAG2, TP53, and U2AF1. Only mutations of SF3B1 were associated with a longer OS at this significance threshold. The large size of the cohort allowed for more precise estimates of survival in less frequently mutated genes. For example, mutations of IDH2 (present in 3.4% of cases, n=103) were associated with shorter OS (hazard ratio [HR] 1.61, 95% confidence interval [CI] 1.26-2.05; p=0.0001) whereas IDH1 mutations (present in 2.4% of cases, n=77) were only marginal (HR 1.29, CI: 0.97-1.72; p=0.082), demonstrating the distinct impact of mutations in these highly related genes. IPSS-R risk groups could be determined for 2173 patients and were strongly associated with OS. Adjusting the hazard ratio of death for IPSS-R risk groups identified several mutated genes with independent prognostic significance: TP53 (HR 2.37, CI 1.94-2.90), CBL (HR 1.57, CI 1.22-2.03), EZH2 (HR 1.55, CI 1.22-2.03), and RUNX1 (HR 1.50, CI 1.24-1.83). Mutations of U2AF1 (HR 1.29, CI 1.06-1.58) and ASXL1 (HR 1.21, CI 1.04-1.41) retained a more modest association with shorter OS. Adjustment for IPSS-R risk groups also moderated the favorable risk associated with mutations of SF3B1 (HR 0.83, CI 0.70-0.99). Patients without mutations in any of the 6 adverse genes above represented 58% of the fully sequenced cohort and had a longer median survival than patients with adverse mutations (4.8 years vs. 1.6 years respectively, p < 0.0001; Figure 2) even after correction for IPSS-R risk groups (adjusted HR 0.59, CI 0.51-0.67). Multivariable analysis of this dataset will examine the combined contribution of mutated genes to prognosis. A mutation score based on survival risk will be proposed and internally validated. The impact of somatic mutation in patients traditionally considered lower risk will be explored. Conclusions This large study definitively validates the prognostic value of mutations in several MDS-associated genes while clarifying the significance of other, less frequently mutated ones. Mutations in several genes retain their prognostic significance after adjustment for IPSS-R risk groups, indicating that these select abnormalities could refine the prediction of prognosis when incorporated into a clinical scoring system such as the IPSS-RM. The results of this analysis will serve as the template with which to build an integrated molecular risk model for MDS. Disclosures Bejar: Alexion: Other: ad hoc advisory board; Celgene: Consultancy, Honoraria; Genoptix Medical Laboratory: Consultancy, Honoraria, Patents & Royalties: MDS prognostic gene signature. Haferlach:MLL Munich Leukemia Laboratory: Employment, Equity Ownership. Sekeres:Celgene Corporation: Membership on an entity's Board of Directors or advisory committees; TetraLogic: Membership on an entity's Board of Directors or advisory committees; Amgen: Membership on an entity's Board of Directors or advisory committees. Fenaux:Celgene Corporation: Honoraria, Research Funding; Amgen: Honoraria, Research Funding; Janssen: Honoraria, Research Funding; Novartis: Honoraria, Research Funding. Kern:MLL Munich Leukemia Laboratory: Employment, Equity Ownership. Shih:Novartis: Research Funding. Komrokji:Celgene: Consultancy, Research Funding; Incyte: Consultancy; Novartis: Research Funding, Speakers Bureau; Pharmacylics: Speakers Bureau. List:Celgene Corporation: Honoraria, Research Funding. Santini:celgene, Janssen, Novartis, Onconova: Honoraria, Research Funding. Campbell:14M genomics: Other: Co-founder and consultant. Ebert:Celgene: Consultancy; Genoptix: Consultancy, Patents & Royalties; H3 Biomedicine: Consultancy.
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Books on the topic "Campbell Committee"

1

Springer, R. Blair. Firefighters: A battle with cancer : a report to Senator William Campbell, chairman, Joint Committee on Fire, Police, Emergency, and Disaster Services. Sacramento, CA: The Committee, 1987.

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Committee, South Carolina General Assembly Insurance Law Study. Report of the Insurance Law Study Committee, April 1988, to the Honorable Carroll A. Campbell, Jr., Governor of South Carolina, the honorable presiding officers and members of the General Assembly. Columbia, S.C: The Committee, 1988.

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Nominations of Anita M. Josey and John M. Campbell: Hearing before the Committee on Governmental Affairs, United States Senate, One Hundred Fifth Congress, first session, on nominations of Anita M. Josey and John M. Campbell, to be asosciate [i.e. associate] judges for the Superior Court of the District of Columbia, October 30, 1997. Washington: U.S. G.P.O., 1998.

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United States. Congress. Senate. Committee on Health, Education, Labor, and Pensions. Subcommittee on Children and Families. Understanding the needs of children and families especially during times of military deployment: Hearing before the Subcommittee on Children and Families of the Committee of Health, Education, Labor and Pensions, United States Senate, One Hundred Eighth Congress, first session on examining how effective the Army has been in making it easier for military families raising children and to determine what additional changes can be made to further assist military families, June 2, 2003 (FT. Campbell, TN). Washington: U.S. G.P.O., 2003.

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Nominations considered during the second session of the 106th Congress: Hearings before the Committee on Environment and Public Works, United States Senate, One Hundred Sixth Congress, second session, on the nomination of Eric D. Eberhard to be a member, Board of Trustees, Morris K. Udall Scholarship and Excellence in National Environmental Policy Foundation, February 3, 2000; the nomination of W. Michael McCabe to be Deputy Administrator, Environmental Protection Agency, February 3, 2000; the nomination of Ella Wong-Ruskinko to be an Alternate Federal co-chair, Appalachian Regional Commission, June 13, 2000; the nomination of Arthur C. Campbell to be Assistant Secretary for Economic Development, Department of Commerce, June 13, 2000; the nomination of James B. Aidala to be Assistant Administrator for Prevention, Pesticides, and Toxic Substances, Environmental Protection Agency, June 13, 2000. Washington: U.S. G.P.O., 2000.

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Report of the Committee of Inquiry into the Care and After-Care of Miss Sharon Campbell. Stationery Office Books, 1988.

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Britain, Great. Public Order Bill: Amendment to be moved in Committee by the Earl ofHalsbury, the Lord Allen Abbeydale, the Lord Campbell of Alloway. London: H.M.S.O., 1986.

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Army family housing: Additional dwelling units not justified at Fort Campbell : report to the Chairman, Subcommittee on Military Construction, Committee on Appropriations, U.S. Senate. Washington, D.C: The Office, 1991.

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Army family housing: Additional dwelling units not justified at Fort Campbell : report to the Chairman, Subcommittee on Military Construction, Committee on Appropriations, U.S. Senate. Washington, D.C: The Office, 1991.

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US GOVERNMENT. Nominations of Anita M. Josey and John M. Campbell: Hearing before the Committee on Governmental Affairs, United States Senate, One Hundred Fifth Congress, ... of Columbia, October 30, 1997 (S. hrg). For sale by the Supt. of Docs., Congressional Sales Office, U.S. G.P.O, 1998.

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Book chapters on the topic "Campbell Committee"

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Lechtreck, Elaine Allen. "New Directions." In Southern White Ministers and the Civil Rights Movement, 144–68. University Press of Mississippi, 2018. http://dx.doi.org/10.14325/mississippi/9781496817525.003.0006.

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This chapter depicts directions far removed from the nonviolent civil rights movement. It includes the rhetoric and actions of New Leaders such as Malcolm X, Stokely Carmichael, Bobby Seale, and James Forman, descriptions of incendiary riots, ministerial responses to the riots, the efforts of Rev. Frank McRae to end the Sanitation Workers Strike in Memphis, King’s assassination, and the dramatic Demand for Reparations. Significant were the responses to the events from Episcopal Bishop John Hines, Rev. Dr. Ralph Sockman, John Morris of the Episcopal Society for Cultural and Racial Unity (ESCRU), W. W. Finlator, Rev. Ed King, and Rabbi James Wax. Also significant were the transformation of Roman Catholic Bishop Joseph Durick, the changes in the Student Nonviolent Coordination Committee (SNCC), and the new directions of Will Campbell who began to see that the racist was perhaps the greatest challenge of the day.
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Maurer, Christian. "Early Enlightenment Shifts." In The History of Scottish Theology, Volume II, 42–55. Oxford University Press, 2019. http://dx.doi.org/10.1093/oso/9780198759348.003.0004.

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This chapter focuses on the tensions concerning doctrinal matters between several Committees for Purity of Doctrine of the Church of Scotland and the three Divinity professors John Simson (1667–1740), Archibald Campbell (1691–1756), and William Leechman (1706–85). It analyses how the themes of innovation, toleration, and rational debate marked theological debates in the early stages of the Scottish Enlightenment. The cases of Simson, Campbell, and Leechman exemplify how in a relatively short time span, the General Assembly and the Kirk started dealing with doctrinal debates concerning orthodoxy and heresy in a more moderate manner, and how the status of the Confession of Faith was subject to discussion, even if there were no proper debates on subscription in eighteenth-century Scotland.
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Graham, Dustin, Isabel Killoran, and Gillian Parekh. "Supporting Students' Mental Health and Emotional Well-Being in Inclusive Classrooms." In Advances in Early Childhood and K-12 Education, 86–116. IGI Global, 2016. http://dx.doi.org/10.4018/978-1-4666-9452-1.ch005.

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Many governments, organizations, and school boards have recently committed to focusing their attention on children's Mental Health and Emotional Well-being (MHEW) (e.g., Kidger, Gunnell, Biddle, Campbell, & Donovan, 2010; Mental Health Commission of Canada, 2013; Ontario Ministry of Education, 2013b). Although often left out of the conversation, teachers play a critical role in supporting and fostering children's MHEW. The purpose of this chapter is threefold: (1) to introduce educators to a critical mental health literacy (CMHL) approach, (2) to identify the teacher's role in supporting MHEW in inclusive classrooms, and (3) to support educators in their efforts to provide inclusive classrooms that accommodate all needs, including MHEW, through the introduction of mindfulness and critical media literacy.
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