To investigate the role of nutritional factors in growth and in the clinical, nutritional, and respiratory status in cystic fibrosis, we studied 12 problem CF patients from six months before to six months after a period of supplemental parenteral nutrition. During the initial six months' observation period on appropriate conventional therapy, the patients (aged 0.5 to 11 years) had inadequate growth and weight gain, a total of 21 active pulmonary infections, and, despite dietary supplements, inadequate ad libitum nutrient intakes. After nutritional therapy, providing a balanced consistent hypercaloric intake for 21 days, catch-up weight gain occurred by one month and continued at six months; catch-up in linear growth was observed by three m...
Cystic fibrosis (CF) is the most common life-threatening autosomal recessive inherited disease in Ca...
Background: A high-calorie diet has been a standard of care in cystic fibrosis (CF) for.3 decades. H...
Optimizing nutrition remains the cornerstone of therapy for patients with cystic fibrosis (CF) since...
Previously, we reported catch-up weight gain, growth, and improved lung function in a group of malno...
Previously, we reported catch-up weight gain, growth, and improved lung function in a group of malno...
The effects of a sustained increase in energy and protein intake on weight gain, growth, body protei...
Effects of nutritional supplements on minimizing weight loss and abnormalities of protein turnover d...
Purpose of review Cystic fibrosis (CF) is a progressive genetic disease that affects multiple organ ...
ABSTRACT. The efficacy and safety of short-term supple-mental peripheral hyperalimentation (PH) was ...
The pulmonary function of patients with cystic fibrosis (CF) is associated with nutritional status n...
AbstractObjectiveTo review the literature addressing the relationship of growth and nutritional para...
Although outcome data for individuals with cystic fibrosis (CF) have shown consistent improvements t...
Abstract Objective: To review the literature addressing the relationship of growth and nutritional ...
PURPOSE OF REVIEW: Cystic fibrosis (CF) is a progressive genetic disease that affects multiple organ...
Cystic fibrosis (CF) is the most commonly occurring lethal autosomal recessive disorder. The gene de...
Cystic fibrosis (CF) is the most common life-threatening autosomal recessive inherited disease in Ca...
Background: A high-calorie diet has been a standard of care in cystic fibrosis (CF) for.3 decades. H...
Optimizing nutrition remains the cornerstone of therapy for patients with cystic fibrosis (CF) since...
Previously, we reported catch-up weight gain, growth, and improved lung function in a group of malno...
Previously, we reported catch-up weight gain, growth, and improved lung function in a group of malno...
The effects of a sustained increase in energy and protein intake on weight gain, growth, body protei...
Effects of nutritional supplements on minimizing weight loss and abnormalities of protein turnover d...
Purpose of review Cystic fibrosis (CF) is a progressive genetic disease that affects multiple organ ...
ABSTRACT. The efficacy and safety of short-term supple-mental peripheral hyperalimentation (PH) was ...
The pulmonary function of patients with cystic fibrosis (CF) is associated with nutritional status n...
AbstractObjectiveTo review the literature addressing the relationship of growth and nutritional para...
Although outcome data for individuals with cystic fibrosis (CF) have shown consistent improvements t...
Abstract Objective: To review the literature addressing the relationship of growth and nutritional ...
PURPOSE OF REVIEW: Cystic fibrosis (CF) is a progressive genetic disease that affects multiple organ...
Cystic fibrosis (CF) is the most commonly occurring lethal autosomal recessive disorder. The gene de...
Cystic fibrosis (CF) is the most common life-threatening autosomal recessive inherited disease in Ca...
Background: A high-calorie diet has been a standard of care in cystic fibrosis (CF) for.3 decades. H...
Optimizing nutrition remains the cornerstone of therapy for patients with cystic fibrosis (CF) since...