Author:
Publisher:
ISBN:
Category :
Languages : en
Pages : 1088
Book Description
Supplement to Lucius H. Hallock's A Hallock genealogy includes biographies of later descendants of Peter Hallock (b. ca. 1590), who may have been one of the first settlers of Southold, Long Island, New York in 1640.
1992 Addendum to A Hallock Genealogy of 1928
Author:
Publisher:
ISBN:
Category :
Languages : en
Pages : 1088
Book Description
Supplement to Lucius H. Hallock's A Hallock genealogy includes biographies of later descendants of Peter Hallock (b. ca. 1590), who may have been one of the first settlers of Southold, Long Island, New York in 1640.
Publisher:
ISBN:
Category :
Languages : en
Pages : 1088
Book Description
Supplement to Lucius H. Hallock's A Hallock genealogy includes biographies of later descendants of Peter Hallock (b. ca. 1590), who may have been one of the first settlers of Southold, Long Island, New York in 1640.
Master Register of Bicentennial Projects, February 1976
Author: American Revolution Bicentennial Administration
Publisher:
ISBN:
Category : American Revolution Bicentennial, 1976
Languages : en
Pages : 572
Book Description
Publisher:
ISBN:
Category : American Revolution Bicentennial, 1976
Languages : en
Pages : 572
Book Description
Vermont Genealogy
Author:
Publisher:
ISBN:
Category : Registers of births, etc
Languages : en
Pages : 510
Book Description
Publisher:
ISBN:
Category : Registers of births, etc
Languages : en
Pages : 510
Book Description
Index of Bicentennial Activities
Author: American Revolution Bicentennial Administration
Publisher:
ISBN:
Category : American Revolution Bicentennial, 1976
Languages : en
Pages : 268
Book Description
Publisher:
ISBN:
Category : American Revolution Bicentennial, 1976
Languages : en
Pages : 268
Book Description
A Brink Book Addendum 1997
Author: Laurel Shanafelt Powell
Publisher:
ISBN:
Category : Dutch Americans
Languages : en
Pages : 162
Book Description
Publisher:
ISBN:
Category : Dutch Americans
Languages : en
Pages : 162
Book Description
The Bicentennial of the United States of America
Author: American Revolution Bicentennial Administration
Publisher:
ISBN:
Category : American Revolution Bicentennial, 1976..
Languages : en
Pages : 540
Book Description
Publisher:
ISBN:
Category : American Revolution Bicentennial, 1976..
Languages : en
Pages : 540
Book Description
The Laws of the State of Vermont
Author: Vermont
Publisher:
ISBN:
Category : Law
Languages : en
Pages : 526
Book Description
Publisher:
ISBN:
Category : Law
Languages : en
Pages : 526
Book Description
Across the Onion
Author: Ellen C. Hill
Publisher:
ISBN:
Category : History
Languages : en
Pages : 392
Book Description
Publisher:
ISBN:
Category : History
Languages : en
Pages : 392
Book Description
Genealogies of Connecticut Families
Author: Judith McGhan
Publisher: Genealogical Publishing Com
ISBN: 0806310308
Category : Connecticut
Languages : en
Pages : 2456
Book Description
Publisher: Genealogical Publishing Com
ISBN: 0806310308
Category : Connecticut
Languages : en
Pages : 2456
Book Description
Registries for Evaluating Patient Outcomes
Author: Agency for Healthcare Research and Quality/AHRQ
Publisher: Government Printing Office
ISBN: 1587634333
Category : Medical
Languages : en
Pages : 385
Book Description
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.
Publisher: Government Printing Office
ISBN: 1587634333
Category : Medical
Languages : en
Pages : 385
Book Description
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.