Zobrazeno 1 - 10
of 66
pro vyhledávání: '"Diane C. Tucker"'
Autor:
Sarah M. Beno, Diane C. Tucker
Publikováno v:
Trends in Teaching Experimentation in the Life Sciences ISBN: 9783030985912
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a01dc7dff7d25cccebfb8999e5054438
https://doi.org/10.1007/978-3-030-98592-9_20
https://doi.org/10.1007/978-3-030-98592-9_20
Autor:
Hanne Würtzen, Christina H. Jagielski, Susanne Oksbjerg Dalton, Christoffer Johansen, Sylvie Mrug, Diane C. Tucker
Publikováno v:
Journal of Psychosocial Oncology. 38:4-19
Purpose: Many clinical interventions have been designed to improve psychological well-being in women with breast cancer; however, there are individual differences in the extent of benefit across participants. Mindfulness-Based Stress Reduction (MBSR)
Autor:
David C. Schwebel, Kimberly Whelan, Avi Madan-Swain, Wendy Demark-Wahnefried, Diane C. Tucker, Margaux B. Gilliam
Publikováno v:
Psycho-Oncology. 22:1361-1368
Objective Determine the extent to which self-efficacy mediates the relations between social support and childhood cancer survivors’ physical activity (PA).
Autor:
Nicole M. Webb, Diane C. Tucker
Publikováno v:
Journal of Palliative Medicine. 12:337-342
Exploring preferences for and barriers to quality end-of-life care is essential to improving care for dying individuals. Young adults often are involved or will be involved in decisions about the care of a loved one, and little research has examined
Autor:
Helen Harrison, Margaret Fadojutimi-Akinsiku, Beverly M. Snively, Shana L. Palla, Diane C. Tucker, Ometha Lewis-Jack, Mark Speechley, Jacob A. Reiss, John H. Eckfeldt, Elizabeth J. Thomson, Charles A. Rivers, Lari Wenzel, Christine E. McLaren, Ebony Bookman, Roger T. Anderson
Publikováno v:
Genetics in Medicine. 9:705-712
The HEIRS Study screened 101,168 primary care participants for iron overload with serum transferrin saturation (TS), serum ferritin (SF), and C282Y and H63D mutations of the HFE gene. The objective of this study was to evaluate the impact of screenin
Autor:
Andrea Ruggiero, Elizabeth J. Thomson, Ann P. Walker, Tara E Power, Lari Wenzel, Diane C. Tucker, Ronald T. Acton, Mark A. Hall, Joan Holup, Barbara Harrison, Catherine Leiendecker-Foster, Roger T. Anderson, Edmund G Howe, Paul C. Adams
Publikováno v:
Genetics in Medicine. 8:681-687
Purpose: Assess the quality of life impact of receiving indeterminate test results for hemochromatosis, a disorder involving HFE genetic mutations and/or elevated serum transferrin saturation and ferritin. Methods: The study sample was from the Hemoc
Autor:
Ronald T. Acton, Nancy Press, Shellie D. Ellis, Elizabeth J. Thomson, Mark A. Hall, Ann P. Walker, Lari Wenzel, Ometha Lewis-Jack, Beverly M. Snively, Roger T. Anderson, Diane C. Tucker
Publikováno v:
Genetics in Medicine. 7:557-563
Purpose: Genetic screening can enable timely detection and treatment of hereditary hemochromatosis (HH). Little is known about patient acceptability of DNA testing as compared to conventional phenotypic testing. Methods: Within the HEIRS Study, a lar
Autor:
Elizabeth J. Thomson, Edmund G Howe, Barbara Harrison, Tara E Power, Jacob A. Reiss, Diane C. Tucker, Mark A. Hall, Gordon D. McLaren, James C. Barton, Ann P. Walker, Andrea Ruggiero, Shellie D. Ellis, Jean E. McEwen
Publikováno v:
Genetics in Medicine. 7:311-316
Purpose: Fear of genetic discrimination might deter participation in research or therapy. This is a major impetus for laws limiting insurers' use of genetic information, yet there is little information about the extent of this fear in the general pop
Publikováno v:
Journal of Behavioral Medicine. 27:491-505
The present study examined the feasibility of evaluating online communication of cancer patients using an automated content analysis program modified for application to cancer-related communication. Public messages posted to the Breast Cancer Discuss
Publikováno v:
Genetic Testing. 8:90-97
We examined attitudes regarding genetic testing and psychosocial outcomes of HFE genotyping for hemochromatosis. A total of 87 persons with hemochromatosis (patients) (39 women, 48 men), who underwent HFE genotyping, and 50 persons with hypertension