<p>Study subgroups: CF-C-PI = CF-causing group, pancreatic insufficient; CF-C-PS = CF-causing group, pancreatic sufficient; VCC = mutations of varying clinical consequence group; and Unk = mutation of unknown liability group. Pancreatic insufficient subjects were removed from VCC (n = 3) and Unk (n = 16) groups for this analysis. There was a statistically significant difference between CF-C-PI and CF-C-PS (p = 0.0247), VCC (p = 0.0013), and Unk (p<0.0001). There is no statistically significance difference between CF-C-PS and VCC and Unk (respectively p = 0.9767 and p = 0.9922). Pairwise comparisons indicate a significant difference of WHZ between CF-C-PI and CF-C-PS, VCC, and Unk at 1m (p<0.0001) and at 6 months (p = 0.0003), and no statist...
OBJECTIVE: To describe pancreatic function during the first year of life in infants diagnosed with c...
We showed elsewhere that the pancreatic function status of cystic fibrosis (CF) patients could be co...
OBJECTIVE: The aim of this study was to evaluate by clinical and laboratory parameters how cystic fi...
To determine the pancreatic phenotype of infants with cystic fibrosis (CF) diagnosed in the first we...
Newborn screening (NBS) for cystic fibrosis (CF) improves nutritional outcomes. Despite early dietet...
Background: We aimed to assess whether final height in children with cystic fibrosis (CF) is affecte...
Newborn screening (NBS) for cystic fibrosis (CF) improves nutritional outcomes. Despite early dietet...
Objectives. To study bone mineral density (BMD) in cystic fibrosis (CF) children and adults with the...
<p>Clinical characteristics in CF patients with pancreatic insufficiency, CF patients with pancreati...
AbstractBackgroundHeight is a strong prognostic factor in cystic fibrosis (CF) and is usually compar...
Background: Poor clinical outcomes in cystic fibrosis are often associated with undernutrition. Nutr...
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the ...
The aim of this study was to describe and compare the nutritional status of children aged 0-18 years...
ACKGROUND & AIMS: Different mutations in the cystic fibrosis gene (CFTR) are associated with di...
OBJECTIVES: Cystic fibrosis transmembrane conductance regulator (CFTR), cationic trypsinogen gene (P...
OBJECTIVE: To describe pancreatic function during the first year of life in infants diagnosed with c...
We showed elsewhere that the pancreatic function status of cystic fibrosis (CF) patients could be co...
OBJECTIVE: The aim of this study was to evaluate by clinical and laboratory parameters how cystic fi...
To determine the pancreatic phenotype of infants with cystic fibrosis (CF) diagnosed in the first we...
Newborn screening (NBS) for cystic fibrosis (CF) improves nutritional outcomes. Despite early dietet...
Background: We aimed to assess whether final height in children with cystic fibrosis (CF) is affecte...
Newborn screening (NBS) for cystic fibrosis (CF) improves nutritional outcomes. Despite early dietet...
Objectives. To study bone mineral density (BMD) in cystic fibrosis (CF) children and adults with the...
<p>Clinical characteristics in CF patients with pancreatic insufficiency, CF patients with pancreati...
AbstractBackgroundHeight is a strong prognostic factor in cystic fibrosis (CF) and is usually compar...
Background: Poor clinical outcomes in cystic fibrosis are often associated with undernutrition. Nutr...
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the ...
The aim of this study was to describe and compare the nutritional status of children aged 0-18 years...
ACKGROUND & AIMS: Different mutations in the cystic fibrosis gene (CFTR) are associated with di...
OBJECTIVES: Cystic fibrosis transmembrane conductance regulator (CFTR), cationic trypsinogen gene (P...
OBJECTIVE: To describe pancreatic function during the first year of life in infants diagnosed with c...
We showed elsewhere that the pancreatic function status of cystic fibrosis (CF) patients could be co...
OBJECTIVE: The aim of this study was to evaluate by clinical and laboratory parameters how cystic fi...