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
Neuroendocrine tumours of head and neck are rare neoplasms and even more rare are those of cutaneous adenoid cystic carcinoma with neuroendocrine differentiation. Virtually every known variant of neoplasia with neuroendocrine differentiation can arise in complex structures of head and neck (Mills in Endocr Pathol 7(4):329-343. doi:10.1007/BF02739841) [1]. Such tumours are usually non functional, locally aggressive and may spread to lymph nodes or lungs. They are diagnosed by histopathology, immunohistochemistry and radionuclide imaging. When these tumours involve the carotid artery, they pose challenges in the surgical management.
Download full-text PDF |
Source |
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6848500 | PMC |
http://dx.doi.org/10.1007/s12070-017-1073-x | DOI Listing |
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