Cystic Fibrosis and Congenital Anomalies of the Exocrine Pancreas

Medicine and Dentistry

• Congenital Malformation 100%
• Cystic Fibrosis 100%
• Exocrine Pancreas 100%
• Patient with Cystic Fibrosis 60%
• Cystic Fibrosis Transmembrane Conductance Regulator 40%
• Exocrine Pancreatic Insufficiency 40%
• Organ Systems 20%
• Autosomal Recessive Disorder 20%
• Liver Disease 20%
• Gastrointestinal Tract 20%
• Lung Function 20%
• Gastrointestinal Distress 20%
• Malabsorption 20%
• Nutritional Status 20%
• Gastrointestinal Disease 20%
• Caloric Intake 20%
• Pancreas Disease 20%
• Energy Expenditure 20%
• Pancreas Enzyme 20%
• Antibiotics 20%
• Lung Clearance 20%
• Nutrition 20%

Keyphrases

• Congenital Anomalies 100%
• Cystic Fibrosis 100%
• Exocrine Pancreas 100%
• Exocrine Pancreatic Insufficiency 42%
• Gastrointestinal Diseases 28%
• Cystic Fibrosis Transmembrane Conductance Regulator 28%
• Genotype 14%
• Antibiotics 14%
• Autosomal Recessive 14%
• Gastrointestinal Tract 14%
• Overall Outcome 14%
• Functional Outcome 14%
• Pancreas 14%
• Nutrition Support 14%
• Pulmonary Function 14%
• Malabsorption 14%
• Nutritional Status 14%
• Multiple Organs 14%
• Energy Expenditure 14%
• Respiratory Tract 14%
• Polycystic Liver Disease 14%
• Pancreatic Diseases 14%
• Caloric Intake 14%
• Pancreatic Enzymes 14%
• Airway Clearance 14%