Zobrazeno 1 - 10
of 81
pro vyhledávání: '"Celia I. Kaye"'
Autor:
John J. Mulvihill, Lori Williamson, Celia I. Kaye, Marc S. Williams, Ann F. Chou, Sylvia Mann
Publikováno v:
Genetics in Medicine. 21:955-964
The Institute of Medicine recommended the utilization of metrics to improve quality in health care, although they have rarely been used in genetics. This study developed and tested a set of metrics for a quality assessment tool for genetic services M
Autor:
Celia I. Kaye, Bruce R. Korf
Publikováno v:
Pediatrics. 132:S224-S230
Since the sequencing of the human genome was completed, progress toward understanding the genetic contributions to both rare and common disorders has accelerated dramatically. That understanding will lead to new approaches to diagnosis and management
Improving Newborn Screening Follow-up in Pediatric Practices: Quality Improvement Innovation Network
Autor:
Barry H. Thompson, Cynthia F. Hinton, Alex R. Kemper, Ruth S. Gubernick, Robert A. Saul, Daniel R. Neuspiel, Jill A. Healy, Celia I. Kaye, Timothy Geleske, Michele A. Lloyd-Puryear
Publikováno v:
Pediatrics. 130:e669-e675
OBJECTIVE: To implement a 6-month quality improvement project in 15 primary care pediatric practices to improve short-term newborn screening (NBS) follow-up. METHODS: At the start of the project, each practice completed a survey to evaluate office sy
Autor:
Susan A. Berry, Celia I. Kaye, Cynthia F. Hinton, Amy Brower, Anne Marie Comeau, Andrea Williams, Kathryn L. Hassell, Jana Monaco, Bradford L. Therrell, Denise Dougherty, Robert J. Ostrander, Christine Brown, Katharine B. Harris, Lisa Feuchtbaum, Carol L. Greene, Nancy S. Green, Charles J. Homer, Alexis A. Thompson, Alan E. Zuckerman
Publikováno v:
Molecular genetics and metabolism. 118(4)
Newborn screening (NBS) is intended to identify congenital conditions prior to the onset of symptoms in order to provide early intervention that leads to improved outcomes. NBS is a public health success, providing reduction in mortality and improved
Autor:
Celia I. Kaye
Publikováno v:
Public Health Genomics. 15:164-171
Identification of genomic determinants of complex disorders such as cancer, diabetes and cardiovascular disease has prompted public health systems to focus on genetic service delivery for prevention of these disorders, adding to their previous effort
Autor:
Dawn Peck, Carolyn Stady Anderson, Judith E Livingston, Dorothy K. Grange, Celia I. Kaye, Maura Taylor, Bradford L. Therrell, Jerome L. Gorski, Sharmini Rogers, Marie Y. Mann, Katherine M. Christensen, Margy Roberston
Publikováno v:
Journal of Community Genetics. 2:191-200
To determine how US newborn dried bloodspot screening (NDBS) programs obtain patient-level data on clinical genetic counseling services offered to families of newborns identified through newborn NDBS and the extent to which newborns and their familie
Autor:
Celia I, Kaye, Robert, Feinstein
Publikováno v:
Academic Medicine. 85:S114-S119
Autor:
Maxine Hayes, Ned Calonge, Kathryn A. Phillips, Ora L. Strickland, Jeffrey R. Botkin, Katrina Armstrong, Joan Scott, Carolyn Sue Richards, James Haddow, Celia I. Kaye, Alfred O. Berg, Margaret Piper, Steven M. Teutsch
Publikováno v:
Genetics in Medicine. 11:15-20
The Evaluation of Genomic Applications in Practice and Prevention (EGAPP) Working Group found that the evidence is currently insufficient to recommend for or against the routine use of UGT1A1 genotyping in patients with metastatic colorectal cancer w
Autor:
Margaret Piper, Carolyn Sue Richards, Jeffrey R. Botkin, Steven M. Teutsch, Kathryn A. Phillips, Alfred O. Berg, James Haddow, Celia I. Kaye, Ora L. Strickland, Katrina Armstrong, Joan Scott, Maxine Hayes, Ned Calonge
Publikováno v:
Genetics in Medicine. 11:66-73
The EGAPP Working Group (EWG) found insufficient evidence to make a recommendation for or against the use of tumor gene expression profiles to improve outcomes in defined populations of women with breast cancer. For one test, the EWG found preliminar
Autor:
Katrina Armstrong, Maxine Hayes, Ned Calonge, Joan Scott, Margaret Piper, Alfred O. Berg, Jeffrey R. Botkin, James Haddow, Celia I. Kaye, Kathryn A. Phillips, Carolyn Sue Richards, Steven M. Teutsch, Ora L. Strickland
Publikováno v:
Genetics in Medicine. 11:35-41