Zobrazeno 1 - 10
of 35
pro vyhledávání: '"K. M. Gil"'
Autor:
K. M. Gil, David H. Elwyn, N. P. D'Attellis, S B Heymsfield, S Bursztein-De Myttenaere, Jeffrey Askanazi, Peter Fürst
Publikováno v:
The American Journal of Clinical Nutrition. 60:244-248
Intravenous administration of nutrients can suppress oral food intake. Inhibition of gastric emptying (GE) is a potential explanation for this process. Inhibition of GE during parenteral nutrition (PN) and attenuation of this by parenteral nutrition
Autor:
L E, Schanberg, M J, Sandstrom, K, Starr, K M, Gil, J C, Lefebvre, F J, Keefe, G, Affleck, H, Tennen
Publikováno v:
Arthritis care and research : the official journal of the Arthritis Health Professions Association. 13(1)
The purpose of this study was 3-fold: 1) to assess the feasibility of a daily diary for use with children with juvenile rheumatic disease (JRD), 2) to describe daily variation in mood, stressful events, and symptoms in children with JRD, and 3) to ex
Publikováno v:
Health psychology : official journal of the Division of Health Psychology, American Psychological Association. 19(1)
This study examined the 3-month follow-up effects of a pain coping skills intervention in African American adults with sickle cell disease. Sixty-seven participants were randomly assigned to either a coping skills condition or a disease-education con
Autor:
J J, Wison Schaeffer, K M, Gil, M, Burchinal, K D, Kramer, K B, Nash, E, Orringer, D, Strayhorn
Publikováno v:
Journal of behavioral medicine. 22(2)
The present study examined depressive symptomatology in 440 adults with sickle cell disease (SCD). Participants completed the Center for Epidemiologic Studies--Depression scale (CES-D) as part of their yearly routine visits to the Duke University--Un
Publikováno v:
Journal of clinical psychology. 54(1)
Illness-specific patterns of adjustment and cognitive adaptational process were identified in children (7-12 years of age) with cystic fibrosis (CF, n = 40) or sickle cell disease (SCD, n = 40). Anxiety diagnoses were most frequent for both illness s
Publikováno v:
Journal of clinical psychology. 52(3)
The stability of psychological adjustment was assessed across three time points spanning a 20-month period with 59 African-American adults with sickle cell anemia. Stable good adjustment was associated with lower levels of daily and illness-related s
Publikováno v:
Arthritis care and research : the official journal of the Arthritis Health Professions Association. 9(2)
The purpose of this study was twofold: 1) to describe the coping strategies used by children with juvenile primary fibromyalgia syndrome (JPFS), and 2) to examine how pain coping relates to measures of pain, disability/function, psychological distres
Publikováno v:
Journal of consulting and clinical psychology. 62(4)
Rates of poor psychological adjustment of children with sickle cell disease remained relatively constant over initial and follow-up assessment points. However, there was relatively little stability in the classification of the adjustment of individua
Publikováno v:
The Clinical journal of pain. 9(2)
The purpose of the present study was to examine factors that influence individual differences in treatment response after multidisciplinary pain management.Pre-post assessment design.119 chronic pain inpatients.Outcome measures included pain report f
Publikováno v:
Journal of consulting and clinical psychology. 61(3)
In this study, 64% of children aged 7-12 years with sickle cell disease were found to have a parent-reported behavior problem, and 50% met the criteria for a Diagnostic and Statistical Manual of Mental Disorders (3rd ed.) diagnosis based on a structu