Malabsorption in children

Practitioner

Volumn 245, Issue 1620, 2001, Pages 162-183

  Lindley, Keith J ^a   Macdonald, Sarah ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL; CYSTIC FIBROSIS; FAILURE TO THRIVE; FOOD ALLERGY; GIARDIASIS; HUMAN; LACTOSE INTOLERANCE; MALABSORPTION; PRESCHOOL CHILD; REVIEW;

ANIMALS; CHILD, PRESCHOOL; CYSTIC FIBROSIS; FAILURE TO THRIVE; FOOD HYPERSENSITIVITY; GIARDIASIS; HUMANS; LACTOSE INTOLERANCE; MALABSORPTION SYNDROMES;

EID: 0041866429     PISSN: 00326518     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (9)

1. Molberg O, Mcadam SN, Korner R et al Tissue transglutaminase selectively modifies gliaden peptides that are recognised by gut-derived T cells in celiac disease. Nature Med 1998;4:713-7
2. Baldas V, Tommasini A, Trevisiol C et al. Development of a novel rapid non-invasive screening test for coeliac disease. Gut 2000;47:628-31
3. Walker-Smith JA, Guandalini S, Schmitz J, Shmerling DH, Visakorpi JK. Revised criteria for the diagnosis of celiac disease. Arch Dis Childhood 1990;65:909-19
4. Anderson RP, Degano P, Godkin AJ, Jewell DP, Hill AVS. In vivo antigen challenge in celiac disease identifies a single transglutaminase-modified peptide as the dominant a-gliaden T-cell epitope. Nature Med 2000;6:337-42
5. Arentz-Hansen H, Korner R, Molberg O et al. The intestinal T cell response to alpha-gliaden in adult celiac disease is focussed on a single deaminated glutamine targeted by tissue transglutaminase. J Exp Med 2000;191:603-12
6. Ellis HJ, Rosen-Bronsen S, O'Reilly N, Ciclitera PJ. Measurement of gluten using a monoclonal antibody to a coeliac toxic peptide of A-gliaden. Gut 1998;43:190-5
7. Maiuri L, Rossi M, Rai V et al. Mosaic regulation of lactase in human adult type hypolactasia. Gastroenterology 1994;107:54-60
8. Harvey CB, Hollox EJ, Poulter M et al. Lactase haplotype frequencies in Caucasians: association with the lactase persistence/non-persistence polymorphism. Am Hum Genet 1998;62:215-23
9. Massir RJ, Wilcken B, Van-Asperen P et al. Pancreatic function and extended mutation analysis in DeltaF508 heterozygous infants with an elevated immunoreactive trypsinogen but abnormal sweat electrolyte levels. J Pediatr 2000;137(2):214-20