Use my Search Websuite to scan PubMed, PMCentral, Journal Hosts and Journal Archives, FullText. Kick-your-searchterm to multiple Engines kick-your-query now !>

A dictionary by aggregated review articles of nephrology, medicine and the life sciences Your one-stop-run pathway from word to the immediate pdf of peer-reviewed on-topic knowledge.

10.3892/ol.2018.8409 http://scihub22266oqcxt.onion/10.3892/ol.2018.8409 C5950510!5950510 !29805581     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=29805581 &cmd=llinks): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 215 Warning: imagejpeg(C:\Inetpub\vhosts\kidney.de\httpdocs\phplern\29805581 .jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117       Oncol+Lett 2018 ; 15 (6 ): 8447-8453 Nephropedia Template TP {{tp|p=29805581 |t=2018. Cronkhite-Canada syndrome: A case report |pdf=|usr=}}{{29805581 }} gab.com Text Cronkhite-Canada syndrome: A case report JO: Oncol Lett http://www.kidney.de/pget.php?&tw=1&pmid=29805581 #FOAvip Cronkhite-Canada syndrome (CCS) is a rare non-inherited condition characterized by gastrointestinal (GI) hamartomatous polyposis, alopecia, onychodystrophy, hyperpigmentation, weight loss and diarrhea. The etiology is most likely autoimmune and diagnosis is based on patient history, physical examination, endoscopic findings of GI polyposis and histology. The disease is very rare; thus far more than 500 cases of CCS have been reported globally. A 58-years-old male with CCS was reported in the present case study. The patient experienced a history of diarrhea and hematochezia for 4 months, with abdominal pain for 1 month and additional nail and toenail loss for half a month. The clinical, endoscopic and histological data confirmed the diagnosis. Twit Text FOAVip Cronkhite-Canada syndrome: A case report ????Oncol Lett http://www.kidney.de/pget.php?&tw=1&pmid=29805581 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=29805581 #FOAvip English Wikipedia <ref>{{Cite pmid|29805581 }}</ref> Cronkhite-Canada syndrome: A case report #MMPMID29805581 Yuan W ; Tian L ; Ai FY ; Liu SJ ; Shen SR ; Wang XY ; Liu F Oncol Lett 2018[Jun]; 15 (6 ): 8447-8453 PMID29805581 show ga Cronkhite-Canada syndrome (CCS) is a rare non-inherited condition characterized by gastrointestinal (GI) hamartomatous polyposis, alopecia, onychodystrophy, hyperpigmentation, weight loss and diarrhea. The etiology is most likely autoimmune and diagnosis is based on patient history, physical examination, endoscopic findings of GI polyposis and histology. The disease is very rare; thus far more than 500 cases of CCS have been reported globally. A 58-years-old male with CCS was reported in the present case study. The patient experienced a history of diarrhea and hematochezia for 4 months, with abdominal pain for 1 month and additional nail and toenail loss for half a month. The clinical, endoscopic and histological data confirmed the diagnosis. äCronkhite-Canada syndrome: A case report (epmc).pdf DeepDyve Pubget Overpricing