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2016
DOI: 10.1016/j.anpede.2015.07.037
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Faecal calprotectin as an aid to the diagnosis of non-IgE mediated cow's milk protein allergy

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Cited by 14 publications
(14 citation statements)
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“…In addition to GI diseases, the FC level was recently used as a diagnostic marker for various atopic and allergic diseases in children. [6][7][8][9][10] In our study, three children with high FC values had allergic diseases, In addition, numerous ongoing studies investigate the relationship of the FC levels with various bowel diseases, such as acute appendicitis, Henoch-Schönlein purpura, and colonic polyps. [23][24][25] Several studies showed that even neonates who suffered from necrotizing enterocolitis had early elevation in FC levels.…”
Section: Discussionmentioning
confidence: 73%
See 3 more Smart Citations
“…In addition to GI diseases, the FC level was recently used as a diagnostic marker for various atopic and allergic diseases in children. [6][7][8][9][10] In our study, three children with high FC values had allergic diseases, In addition, numerous ongoing studies investigate the relationship of the FC levels with various bowel diseases, such as acute appendicitis, Henoch-Schönlein purpura, and colonic polyps. [23][24][25] Several studies showed that even neonates who suffered from necrotizing enterocolitis had early elevation in FC levels.…”
Section: Discussionmentioning
confidence: 73%
“…In addition to GI diseases, the FC level was recently used as a diagnostic marker for various atopic and allergic diseases in children . In our study, three children with high FC values had allergic diseases, one 34‐month‐old child with high FC value was diagnosed with cow's milk protein allergy, and other 24‐month‐old and 29‐month‐old children without food allergy had a history of atopic dermatitis.…”
Section: Discussionmentioning
confidence: 74%
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“…Therefore, gut proteins such as β-defensin, eosinophil cationic protein, TNF-α, and calprotectin in fecal samples can act as surrogate markers of cellular response. The Table lists studies showing that estimation of FC may prove to be a useful biomarker in FPIES [2,4,5]. Beşer et al [4] showed a higher FC level in non-IgE-mediated disease before elimination of CMP that decreased after elimination of CMP, although levels were still higher than in IgE-mediated disease.…”
mentioning
confidence: 99%