Severity: Warning
Message: file_get_contents(https://...@pubfacts.com&api_key=b8daa3ad693db53b1410957c26c9a51b4908&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 176
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 176
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 250
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 1034
Function: getPubMedXML
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3152
Function: GetPubMedArticleOutput_2016
File: /var/www/html/application/controllers/Detail.php
Line: 575
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 489
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 316
Function: require_once
Abstract Objectives: Because of its specificity for nerve fibers of the enteric nervous system, calretinin is an effective adjunctive marker in the assessment for Hirchsprung disease. Growth associated protein (GAP-43) has been shown to be expressed in nerve fibers within the intestinal lamina propria. No prior report compares GAP-43 expression in ganglionic versus aganglionic intestine. Methods: Six consecutive Hirschsprung endorectal pull through specimens were retrieved from our archives. In addition 3 controls were selected from colonic resections for reasons other than Hirschsprung Disease. Immunoperoxidase for GAP-43 was carried out on the ganglionic and aganglionic segments of all cases and controls. Submucosal ganglion soma positivity and nerve fiber positivity within the lamina propria were graded on a subjective scale of 1-3 that incorporated both strength and density. Data: GAP-43 strongly stained submucosal ganglion cells and nerve fibers within the lamina propria in 6/6 of the ganglionic segments and 3/3 of the normally innervated controls . GAP-43 did not show any ganglion cell body positivity within the aganglionic segments; however, all 6 aganglionic segment lamina propria were positive for nerve fiber staining. There was a small subjective increase in the amount of nerve fiber positivity for GAP-43 in ganglionic segments and controls versus aganglionic segments. Conclusion: GAP-43 marks mucosal nerve fibers in ganglionic intestine but also aganglionic intestine and thus is less useful than calretinin as a marker for Hirschsprung Disease. The abundant mucosal nerves highlighted by GAP-43 requires further characterization.
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Source |
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http://dx.doi.org/10.2350/12-06-1213-OA.1 | DOI Listing |
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