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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...
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...
Detection of Cystic Fibrosis DF508 Mutation in the Çukurova Region
Mutation Cystic Fibrosis Ç ukurova Region
2009/6/29
Cystic fibrosis (CF) is a well-known inherited multisystem disorder characterised primarily by chronic obstructive lung disease and maldigestion. The frequency of the disease varies among ethnic group...
Acute pancreatitis as an atypical presentation of Henoch-Schonlein purpura and cystic fibrosis
acute pancreatitis cystic fibrosis Henoch-Schonlein purpura
2010/1/12
Acute pancreatitis (AP) is a rare clinical entity in childhood. Two children, aged 10 and 14 years, were hospitalized for acute abdominal pain. Clinical and laboratory findings were compatible with AP...
Immunolocalization and Regulation of Cystic Fibrosis Transmembrane Conductance Regulator in the Adult Rat Epididymis
Principal and clear cells orchidectomy efferent duct ligation lumicrine testicular factor
2008/12/22
Cystic fibrosis is the most common serious autosomal recessive condition in whites, and more than 95% of men with cystic fibrosis are infertile. The cystic fibrosis transmembrane conductance regul...
Vitamin D insufficiency in children, adolescents, and young adults with cystic fibrosis despite routine oral supplementation1,2,3
Cystic fibrosis vitamin D fat-soluble vitamins children adolescents
2008/12/17
Background: Cystic fibrosis (CF) with pancreatic insufficiency is associated with poor absorption of fat and fat-soluble vitamins, including vitamin D. Pancreatic enzyme supplementation does not compl...
Evaluation of formulas for calculating total energy requirements of preadolescent children with cystic fibrosis
Doubly labeled water validation energy expenditure energy requirement cystic fibrosis
2008/12/12
Background: To support age-appropriate growth and to prevent and treat malnutrition in children with cystic fibrosis (CF), energy requirements for those children are often set above the requirements f...
