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
Juvenile ossifying fibroma is a benign lesion with aggressive local growth. It is similar to an ossifying fibroma, although it is more aggressive and of earlier onset. Some cases of ossifying fibroma are part of a syndrome that includes hyperparathyroidism (caused by adenoma or carcinoma) and renal lesions, possibly caused by a recently discovered genetic mutation. These tumours must be treated by radical excision, to prevent recurrence. We report a case of recurrent juvenile ossifying fibroma, in an 18-year-old girl. The treatment was radical en-bloc resection, which was reconstructed at the same operation with an iliac crest bone graft. After one year, there has been satisfactory integration of the graft and the teeth have been implanted.
Download full-text PDF |
Source |
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http://dx.doi.org/10.1016/j.bjoms.2007.11.007 | DOI Listing |
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