Autograph Card Signed W.J. To: "Miss M.W. Calkins"
Author : William James
Publisher :
Page : 1 pages
File Size : 32,37 MB
Release : 1907
Category :
ISBN :
Author : William James
Publisher :
Page : 1 pages
File Size : 32,37 MB
Release : 1907
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Author : William James
Publisher :
Page : 1 pages
File Size : 34,70 MB
Release : 1904
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Author : William James
Publisher :
Page : 4 pages
File Size : 49,65 MB
Release : 1909
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Author : William James
Publisher :
Page : 6 pages
File Size : 35,53 MB
Release : 1907
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Author : May Sinclair
Publisher :
Page : 5 pages
File Size : 25,77 MB
Release : 1918
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Author : Charles Dudley Warner
Publisher :
Page : 2 pages
File Size : 45,95 MB
Release : 1886
Category :
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Author : William James
Publisher :
Page : 4 pages
File Size : 10,12 MB
Release : 1908
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Author : Henry James
Publisher :
Page : 1 pages
File Size : 21,9 MB
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Author : Thomas Kren
Publisher : Getty Publications
Page : 273 pages
File Size : 45,35 MB
Release : 1992-07-16
Category : Art
ISBN : 0892362049
Presented at a symposium held in 1990 to celebrate the Getty Museum's acquisition of the only known illuminated copy of The Visions of Tondal, twenty essays address the celebrated bibliophilic activity of Margaret of York; the career of Simon Marmion, a favorite artist of the Burgundian court; and The Visions of Tondal in relation to illustrated visions of the Middle Ages. Contributors include Maryan Ainsworth, Wim Blockmans, Walter Cahn, Albert Derolez, Peter Dinzelbacher, Rainald Grosshans, Sandra Hindman, Martin Lowry, Nigel Morgan, and Nigel Palmer.
Author : Agency for Healthcare Research and Quality/AHRQ
Publisher : Government Printing Office
Page : 385 pages
File Size : 34,61 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.