Association between celiac disease and primary lactase deficiency

[1]  U. Ghoshal,et al.  Frequency of lactose malabsorption among healthy southern and northern Indian populations by genetic analysis and lactose hydrogen breath and tolerance tests. , 2010, The American journal of clinical nutrition.

[2]  C. Borgna-Pignatti,et al.  Genetic testing for adult-type hypolactasia in Italian families , 2008, Clinical chemistry and laboratory medicine.

[3]  D. Schuppan,et al.  Etiologies and predictors of diagnosis in nonresponsive celiac disease. , 2007, Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association.

[4]  E. Seidman,et al.  Guideline for the Diagnosis and Treatment of Celiac Disease in Children : Recommendations of the North American Society for Pediatric Gastroenterology , Hepatology and Nutrition , 2004 .

[5]  D. Swallow.  Genetics of lactase persistence and lactose intolerance. , 2003, Annual review of genetics.

[6]  I. Järvelä,et al.  Transcriptional regulation of the lactase-phlorizin hydrolase gene by polymorphisms associated with adult-type hypolactasia , 2003, Gut.

[7]  Leena Peltonen,et al.  Identification of a variant associated with adult-type hypolactasia , 2002, Nature Genetics.

[8]  American Academy of Pediatrics Committee on Nutrition: Practical significance of lactose intolerance in children: supplement. , 1990, Pediatrics.

[9]  L. Bolund,et al.  The human lactase‐phlorizin hydrolase gene is located on chromosome 2 , 1988, FEBS letters.

[10]  N. Kretchmer.  Lactose and lactase--a historical perspective. , 1971, Gastroenterology.