Lactose malabsorption is a risk factor for decreased bone mineral density in pancreatic insufficient cystic fibrosis patients - Mądry, Edyta; Krasińska, Beata; Drzymała-Czyż, Sławomira; Sands, Dorota; Lisowska, Aleksandra; Grebowiec, Philip; Minarowska, Alina; Oralewska, Beata; Mańkowski, Przemyslaw; Moczko, Jerzy; Walkowiak, Jarosław (European journal of human genetics : EJHG, 2012)
Keywords: Adult; Biological and medical sciences; Body Weight; Bone Demineralization, Pathologic - etiology; Bone Demineralization, Pathologic - genetics; Bone density; Bone Density - genetics; Bone mineral density; Breath Tests; Calcium; Calcium - metabolism; Child; Cholecalciferol - blood; Cholestasis; Cirrhosis; Cystic fibrosis; Cystic Fibrosis - complications; Diabetes mellitus; Fatty liver; Female; Fibrosis; Fundamental and applied biological sciences. Psychology; Gastroenterology. Liver. Pancreas. Abdomen; Gene polymorphism; Genetics of eukaryotes. Biological and molecular evolution; Genotypes; Glucocorticoids; Humans; Lactase; Lactase - deficiency; Lactase - genetics; Lactose; Lactose Intolerance - complications; Lactose Intolerance - genetics; Liver; Lung; Malabsorption; Male; Medical genetics; Medical sciences; Methane; Milk; Milk products; Minerals; Molecular and cellular biology; Nutrition; Nutritional status; Other diseases. Semiology; Pancreas; Polymorphism, Single Nucleotide; Promoter Regions, Genetic - genetics; Regression analysis; Risk Factors; Short Report; Single-nucleotide polymorphism; Statistical analysis; Steatosis; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus; Teenagers; Vitamin D; Vitamin D3; Vitamins; Young adults; Poland; Human; Respiratory disease; Metabolic diseases; Patient; Cystic fibrosis; lactose malabsorption; Genetic disease; Lactose; Intestinal malabsorption; adult-type hypolactasia; Risk factor; Digestive diseases; Intestinal disease; Adult; Genetics; Bone mineral density; Pancreas; Pancreatic disease