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Combined Exercise Training Improves Glycemic Control in Adult with Cystic Fibrosis
CYSTIC FIBROSIS–RELATED DIABETES TRAINING GLUCOSE TOLERANCE DYSGLYCEMIA
2018/4/24
Purpose Glucose abnormality and diabetes are the most common comorbidities in cystic fibrosis (CF). Combined (aerobic and resistance) exercise program in type 2 patients with diabetes demonstrated an ...
Diminished and erratic absorption of ergocalciferol in adult cystic fibrosis patients
Vitamin D cystic fibrosis malabsorption
2016/6/13
Osteoporosis diminishes the quality of life in
adults with cystic fibrosis (CF). Vitamin D deficiency resulting
from malabsorption may be a factor in the etiology of low bone
mineral density (BMD) ...
Patients with cystic fibrosis (CF) are at risk of
developing vitamin K deficiency because of pancreatic insufficiency,
hepatobiliary disease, or both.
Energy expenditure and substrate utilization in adults with cystic fibrosis and diabetes mellitus
Cystic fibrosis diabetes mellitus energy expenditure
2016/5/31
The onset of cystic fibrosis–related diabetes mellitus
(CFDM) is often associated with a decline in clinical and
nutritional status.
Comparison of growth status of patients with cystic fibrosis between the United States and Canada
Cystic fibrosis growth height percentile
2016/5/30
Differences in growth status of patients with cystic
fibrosis (CF) between the United States and Canada were
reported in the 1980s based on analysis of data from 2 regional
CF centers.
Fat malabsorption in cystic fibrosis patients receiving enzyme replacement therapy is due to impaired intestinal uptake of long-chain fatty acids
fat malabsorption fat balance lipolysis
2016/5/27
Pancreatic enzyme replacement therapy frequently
fails to correct intestinal fat malabsorption completely in
cystic fibrosis (CF) patients. The reason for this failure is
unknown.
A Possible Alternative Exercise Test for Youths with Cystic Fibrosis: The Steep Ramp Test
PULMONARY DISEASE EXERCISE TESTING EXERCISE CAPACITY REHABILITATION PHYSIOLOGY
2017/4/14
Purpose: The steep ramp test (SRT) can be used to provide an indication of exercise capacity when gas exchange measurements are not possible. This study evaluated the clinical usefulness of the SRT in...
Exercise testing and training with the young cystic fibrosis patient
Cystic fibrosis young patients exercise testing
2015/4/2
The purpose of the article is to review the literature related to
exercise and Cystic fibrosis (CF), with particular focus on the
young CF patient. Exercise intolerance is a characteristic of CF, ...
Impaired Aerobic Function in Patients with Cystic Fibrosis during Ramp Exercise
NEAR-INFRARED,SPECTROSCOPY AEROBIC,FUNCTION EXERCISE,TESTING EXERCISE,LIMITATION LUNG,DISEASE PEDIATRICS
2017/5/25
This study aimed to document the matching of muscle O2 delivery to O2 use in young patients with cystic fibrosis (CF) from muscle deoxygenation (HHb) dynamics during ramp exercise.
The Role of Bacteriocins in Mediating Interactions of Bacterial Isolates from Cystic Fibrosis Patients
Bacteriocin Burkholderia cepacia complex Cystic Fibrosis Pseudomonas aeruginosa
2014/12/10
Cystic Fibrosis (CF) is a common autosomal genetic disorder in Caucasian populations. CF is caused by mutations in the cftr gene, which encodes the CF transmembrane conductance regulator (CFTR). CFTR ...
Prediction of Mortality in Adolescents with Cystic Fibrosis
CYSTIC,FIBROSIS MORTALITY EXERCISE,CAPACITY NUTRITIONAL,STATUS LUNG,FUNCTION
2017/5/24
Lung function, nutritional status, and parameters of exercise capacity are known predictors of mortality in patients with cystic fibrosis (CF). The aim of the current study was to use these important ...
NHMRC funds The University of Queensland research into kidney disease, cystic fibrosis and more
chronic kidney disease respiratory illness
2014/7/14
The University of Queensland was today awarded more than $51 million in National Health and Medical Research Council grants that will fund research projects investigating health issues such as cystic ...
Infantile convulsions due to hyponatremia caused by Cystic Fibrosis
Cystic fibrosis Infantile convulsions
2009/12/31
Cystic Fibrosis (CF) is an inherited multisystem disorder of children and adults. Characterized chiefly by chronic obstruction and infection of airways, maldigestion and its consequences. It is the mo...
Quantitative and O2 Enhanced MRI of the Pathologic Lung: Findings in Emphysema, Fibrosis, and Cystic Fibrosis
the Pathologic Lung Emphysema Cystic Fibrosis
2009/9/7
Purpose: beyond the pure morphological visual representation, MR imaging offers the possibility to quantify parameters in the healthy, as well as, in pathologic lung parenchyma. Gas exchange is the pr...
Neutrophil chemotaxis in acutely infected and clinically stable cystic fibrosis patients
Cystic fibrosis neutrophils chemotaxis
2009/7/1
Brochopulmonary infection in cystic fibrosis (CF) patients is associated with chronic progressive lung disease. The role of host factors, such as neutrophil functions, in the progressive pathologic pr...