Background: Cystic fibrosis is a multisystemic disorder. It is the most common autosomal recessive disorder in whites that causes complications such as changes in bone density. Therefore, evaluating bone densitometry and serum levels of vitamin D in children with cystic fibrosis is the aim of our study. Methods: This study was performed on 54 children with cystic fibrosis. After recording demographic information, bone densitometry and serum levels of vitamin D were recorded. Chi-square and Pearson correlation tests were used to compare data. Results: Based on our study 53.7% of patients with CF had vitamin D less than 20 nmol / l. It was also found that based on lumbar BMD, 20.3% had a BMD less than 2.5 - Based on femoral BMD, 18.5% had a B...
Background: Cystic fibrosis (CF) with pancreatic insufficiency is associated with poor absorption of...
The objective of the study is to evaluate alterations of bone metabolism in adolescence and adult CF...
This is the author accepted manuscript. The final version is available from Elsevier via the DOI in ...
Cystic fibrosis is the most common genetic disease that causes respiratory failure and earlydeath. T...
The objective of this study was to investigate the extent to which vitamin D and K are associated wi...
BACKGROUND: Low bone mineral density (BMD) is recognised in individuals with cystic fibrosis (CF) al...
Background: We aimed to describe the longitudinal changes in bone mineral content and influencing f...
An alarming incidence of low bone mineral density (BMD) has been identified in individuals with cyst...
Cystic Fibrosis is the most common inherited genetic respiratory disorder in the Western World. Hypo...
Cystic Fibrosis is the most common inherited genetic respiratory disorder in the Western World. Hypo...
Abnormalities of calcium and vitamin D metabolism in cystic fibrosis (CF) are well documented. We te...
Background—Patients with cystic fibrosis have several risk factors for the develop-ment of low bone ...
© 2018 SENPE and Arán Ediciones S.L. Background: cystic fibrosis (CF) is the most common inherited d...
AbstractBackgroundLow bone mineral density is common in adults with cystic fibrosis. Children with g...
Patients with cystic fibrosis (CF) have an increasing life span and osteoporosis has become a more r...
Background: Cystic fibrosis (CF) with pancreatic insufficiency is associated with poor absorption of...
The objective of the study is to evaluate alterations of bone metabolism in adolescence and adult CF...
This is the author accepted manuscript. The final version is available from Elsevier via the DOI in ...
Cystic fibrosis is the most common genetic disease that causes respiratory failure and earlydeath. T...
The objective of this study was to investigate the extent to which vitamin D and K are associated wi...
BACKGROUND: Low bone mineral density (BMD) is recognised in individuals with cystic fibrosis (CF) al...
Background: We aimed to describe the longitudinal changes in bone mineral content and influencing f...
An alarming incidence of low bone mineral density (BMD) has been identified in individuals with cyst...
Cystic Fibrosis is the most common inherited genetic respiratory disorder in the Western World. Hypo...
Cystic Fibrosis is the most common inherited genetic respiratory disorder in the Western World. Hypo...
Abnormalities of calcium and vitamin D metabolism in cystic fibrosis (CF) are well documented. We te...
Background—Patients with cystic fibrosis have several risk factors for the develop-ment of low bone ...
© 2018 SENPE and Arán Ediciones S.L. Background: cystic fibrosis (CF) is the most common inherited d...
AbstractBackgroundLow bone mineral density is common in adults with cystic fibrosis. Children with g...
Patients with cystic fibrosis (CF) have an increasing life span and osteoporosis has become a more r...
Background: Cystic fibrosis (CF) with pancreatic insufficiency is associated with poor absorption of...
The objective of the study is to evaluate alterations of bone metabolism in adolescence and adult CF...
This is the author accepted manuscript. The final version is available from Elsevier via the DOI in ...