Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Paula J. Anderson"'
Autor:
Laura D Wagner, Allen C. Sherman, Dianne Campbell, Bethany Guinee, Catherine E. O'Brien, Paula J. Anderson, Stephanie Simonton-Atchley, Raghu M Reddy
Publikováno v:
Journal of Behavioral Medicine. 43:596-604
Individuals with cystic fibrosis (CF) are confronted by a range of difficult physical and psychosocial sequelae. Gratitude has drawn growing attention as a psychosocial resource, but it has yet to be examined among adults with CF. The current investi
Autor:
Bethany Guinee, Allen C. Sherman, Raghu M Reddy, Laura D Wagner, Catherine E. O'Brien, Stephanie Simonton-Atchley, Dianne Campbell, Paula J. Anderson
Publikováno v:
Journal of Religion and Health.
Individuals with cystic fibrosis (CF) face a challenging disease, and depression is a significant concern. Many patients draw on religious/spiritual resources to assist them in managing the demands of chronic illness; however, these coping efforts ra
Autor:
Allen C, Sherman, Stephanie, Simonton-Atchley, Catherine E, O'Brien, Dianne, Campbell, Raghu M, Reddy, Bethany, Guinee, Laura D, Wagner, Paula J, Anderson
Publikováno v:
Journal of religion and health. 60(4)
Individuals with cystic fibrosis (CF) face a challenging disease, and depression is a significant concern. Many patients draw on religious/spiritual resources to assist them in managing the demands of chronic illness; however, these coping efforts ra
Autor:
Marcia L. Erbland, Nicolaas E. P. Deutz, Renate Jonker, Paula J. Anderson, Mariëlle P.K.J. Engelen
Publikováno v:
Metabolism. 69:120-129
Background The development of effective nutritional strategies in support of muscle growth for patients with chronic obstructive pulmonary disease (COPD) remains challenging. Dietary essential amino acids (EAAs) are the main driver of postprandial ne
Autor:
Bethany Guinee, Raghu M Reddy, Laura D Wagner, Stephanie Simonton-Atchley, Allen C. Sherman, Dianne Campbell, Catherine E. O'Brien, Paula J. Anderson
Publikováno v:
Respiratory care. 64(7)
BACKGROUND: Airway clearance therapy (ACT) is a core component of daily treatment for cystic fibrosis (CF). However, surprisingly little is known about sustained or persistent use of ACT over time among adults with CF. This longitudinal study examine
Autor:
Marcia L. Erbland, Nicolaas E. P. Deutz, Mariëlle P.K.J. Engelen, Paula J. Anderson, Renate Jonker
Publikováno v:
The American Journal of Clinical Nutrition. 103:1458-1464
Background: Chronic obstructive pulmonary disease (COPD) is a condition characterized by systemic low-grade inflammation that could increase the production of nitric oxide (NO), of which arginine is the sole precursor. Arginine is derived from the br
Publikováno v:
Clinical Nutrition. 33:1024-1032
Adequate protein intake and digestion are necessary to prevent muscle wasting in cystic fibrosis (CF). Accurate and easy-to-use methodology to quantify protein maldigestion is lacking in CF.To measure protein digestibility and the response to pancrea
Autor:
Nicolaas E. P. Deutz, Mariëlle P.K.J. Engelen, Renate Jonker, Marcia L. Erbland, Paula J. Anderson
Publikováno v:
Clinical Nutrition. 33:211-220
Muscle wasting commonly occurs in COPD, negatively affecting outcome. The aim was to examine the net whole-body protein synthesis response to two milk protein meals with comparable absorption rates (hydrolyzed casein (hCAS) vs. hydrolyzed whey (hWHEY
Autor:
Krishna Kakkera, Nishi Shah, Kshitij Chatterjee, Rajani Jagana, Paula J. Anderson, Abhinav Goyal
Publikováno v:
Advances in Respiratory Medicine; Volume 84; Issue 6; Pages: 316-323
Introduction: Cystic fibrosis (CF) is a life-limiting multisystemic genetic disease. Patients with CF have a high rate of hospitalization. We attempt to ascertain national trends of inpatient stays, prevalence of various co-morbidities during hospita
Publikováno v:
Journal of the American Academy of Nurse Practitioners. 24:625-632
Purpose: To discuss the role of the nurse practitioner in medical management of adult patients with cystic fibrosis (CF). Data sources: A systematic literature review was done by searching online databases: CINAHYL, OVID, and Medline. The Cystic Fibr