Author : National Library of Medicine (U.S.)
Publisher :
Page : 1442 pages
File Size : 20,14 MB
Release : 1983
Category : Medicine
ISBN :
First multi-year cumulation covers six years: 1965-70.
Author : Mari Sandoz
Publisher : U of Nebraska Press
Page : 356 pages
File Size : 30,21 MB
Release : 1982-01-01
Category : History
ISBN : 9780803291263
First published in the dark days immediately before World War II, Capital City is Mari Sandoz's angriest and most political novel. Like many important American novels of the 1930s?John Steinbeck's The Grapes of Wrath, John Conroy's The Disinherited, Robert Cantwell's Land of Plenty?Capital City depicts the troubles and responses of working people trapped in the Great Depression. It is a unique portrayal of the depression in the Great Plains, and a study of the forces that bitterly contended for wealth and power. Sandoz researched the daily life and behind-the-scenes operations of several state capitals in the thirties before drawing them together in this novel, part allegory, part indictment, part warning. Famous for her passionate writing, Sandoz gave Capital City the full measure of ferocity and rage.
Author : Laure Sandoz
Publisher : Springer Nature
Page : 253 pages
File Size : 22,96 MB
Release : 2019-08-21
Category : Social Science
ISBN : 3030211223
This open access book analyses the strategies of migration intermediaries from the public and private sectors in Switzerland to select, attract, and retain highly skilled migrants who represent value to them. It reveals how state and economic actors define “wanted immigrants” and provide them with privileged access to the Swiss territory and labour market. The analysis draws on an ethnographic study conducted in the French-speaking Lake Geneva area and the German-speaking northwestern region of Switzerland between 2014 and 2018. It shows how institutional actors influence which resources are available to different groups of newcomers by defining and dividing migrants according to constructed social categories that correlate with specific status and privileges. This research thus shifts the focus from an approach that takes the category of highly skilled migrant for granted to one that regards context as crucial for structuring migrants’ characteristics, trajectories, and experiences. Beyond consideration of professional qualifications, the ways decision-makers perceive candidates and shape their resource environments are crucial for constructing them as skilled or unskilled, wanted or unwanted, welcome or unwelcome.
Author : National Library of Medicine (U.S.)
Publisher :
Page : 1118 pages
File Size : 33,62 MB
Release : 1979
Category : Medicine
ISBN :
A keyword listing of serial titles currently received by the National Library of Medicine.
Author : Agency for Healthcare Research and Quality/AHRQ
Publisher : Government Printing Office
Page : 385 pages
File Size : 36,55 MB
Release : 2014-04-01
Category : Medical
ISBN : 1587634333
This User’s Guide is intended to support the design, implementation, analysis, interpretation, and quality evaluation of registries created to increase understanding of patient outcomes. For the purposes of this guide, a patient registry is an organized system that uses observational study methods to collect uniform data (clinical and other) to evaluate specified outcomes for a population defined by a particular disease, condition, or exposure, and that serves one or more predetermined scientific, clinical, or policy purposes. A registry database is a file (or files) derived from the registry. Although registries can serve many purposes, this guide focuses on registries created for one or more of the following purposes: to describe the natural history of disease, to determine clinical effectiveness or cost-effectiveness of health care products and services, to measure or monitor safety and harm, and/or to measure quality of care. Registries are classified according to how their populations are defined. For example, product registries include patients who have been exposed to biopharmaceutical products or medical devices. Health services registries consist of patients who have had a common procedure, clinical encounter, or hospitalization. Disease or condition registries are defined by patients having the same diagnosis, such as cystic fibrosis or heart failure. The User’s Guide was created by researchers affiliated with AHRQ’s Effective Health Care Program, particularly those who participated in AHRQ’s DEcIDE (Developing Evidence to Inform Decisions About Effectiveness) program. Chapters were subject to multiple internal and external independent reviews.
Author :
Publisher :
Page : 1060 pages
File Size : 37,57 MB
Release : 1993
Category : Cancer
ISBN :
Author : Library of Congress
Publisher :
Page : 1034 pages
File Size : 16,10 MB
Release : 1979
Category :
ISBN :
Author : Amos Bad Heart Bull
Publisher :
Page : 0 pages
File Size : 22,12 MB
Release : 2017
Category : History
ISBN : 9781496203595
"Originally published in 1967, this remarkable pictographic history consists of more than four hundred drawings and script notations by Amos Bad Heart Bull, an Oglala Lakota man from the Pine Ridge Reservation, made between 1890 and the time of his death in 1913. The text, resulting from nearly a decade of research by Helen H. Blish and originally presented as a three-volume report to the Carnegie Institution, provides ethnological and historical background and interpretation of the content. This 50th anniversary edition provides a fresh perspective on Bad Heart Bull's drawings through digital scans of the original photographic plates created when Blish was doing her research. Lost for nearly half a century--and unavailable when the 1967 edition was being assembled--the recently discovered plates are now housed at the Smithsonian's National Anthropological Archives. Readers of the volume will encounter new introductions by Emily Levine and Candace S. Greene, crisp images and notations, and additional material that previously appeared only in a limited number of copies of the original edition." -- Publisher's website.
Author : National Institutes of Health (U.S.)
Publisher :
Page : 532 pages
File Size : 32,51 MB
Release : 1990
Category :
ISBN :
Author : Institute of Medicine
Publisher : National Academies Press
Page : 135 pages
File Size : 31,1 MB
Release : 2000-04-07
Category : Medical
ISBN : 0309183642
The Institute of Medicine's (IOM's) Roundtable on Research and Development of Drugs, Biologics, and Medical Devices evolved from the Forum on Drug Development, which was established in 1986. Sponsor representatives and IOM determined the importance of maintaining a neutral setting for discussions regarding long-term and politically sensitive issues justified the need to revise and enhance past efforts. The new Roundtable is intended to be a mechanism by which a broad group of experts from the public* and private sectors can be convened to conduct a dialogue and exchange information related to the development of drugs, biologics, and medical devices. Members have expertise in clinical medicine, pediatrics, clinical pharmacology, health policy, health insurance, industrial management, and product development; and they represent interests that address all facets of public policy issues. From time to time, the Roundtable requests that a workshop be conducted for the purpose of exploring a specific topic in detail and obtaining the views of additional experts. The first workshop for the Roundtable was held on April 14 and 15, 1998, and was entitled Assuring Data Quality and Validity in Clinical Trials for Regulatory Decision Making. The summary on that workshop is available from IOM. This workshop summary covers the second workshop, which was held on May 24 and 25, 1999, and which was aimed at facilitating the development and proper use of drugs, biologics, and medical devices for infants and children. It explores the scientific underpinnings and clinical needs, as well as the regulatory, legal, and ethical issues, raised by this area of research and development.
