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10.1007/s12663-013-0474-y http://scihub22266oqcxt.onion/10.1007/s12663-013-0474-y C4379220!4379220!25861190     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=25861190&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       J+Maxillofac+Oral+Surg 2015 ; 14 (Suppl 1): 258-62 Nephropedia Template TP {{tp|p=25861190|t=2015. Cherubism: A Case Report |pdf=|usr=}}{{25861190}} gab.com Text Cherubism: A Case Report JO: J Maxillofac Oral Surg http://www.kidney.de/pget.php?&tw=1&pmid=25861190 #FOAvip Cherubism is a benign, self-limiting fibro-osseous lesion characterized by bilateral symmetric painless expansion of jaw which is more prominent in mandible than in maxilla. Males are commonly affected (2:1) and with greater severity. It becomes noticeable in early childhood and gradually regresses after puberty. Although cherubism is considered as a familial/inherited disease but many sporadic cases have been reported in literature with no familial history. Osteoblastic and osteoclastic remodeling replaces normal bone by excessive amount of fibrovascular tissue containing multinucleated giant cells. Here, we present a case report of cherubism in a 10 year old boy describing the clinical, histological, biochemical and radiographic features. Twit Text FOAVip Cherubism: A Case Report ????J Maxillofac Oral Surg http://www.kidney.de/pget.php?&tw=1&pmid=25861190 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=25861190 #FOAvip English Wikipedia <ref>{{Cite pmid|25861190}}</ref> Cherubism: A Case Report #MMPMID25861190 Degala S; Mahesh KP; Monalisha J Maxillofac Oral Surg 2015[Mar]; 14 (Suppl 1): 258-62 PMID25861190show ga Cherubism is a benign, self-limiting fibro-osseous lesion characterized by bilateral symmetric painless expansion of jaw which is more prominent in mandible than in maxilla. Males are commonly affected (2:1) and with greater severity. It becomes noticeable in early childhood and gradually regresses after puberty. Although cherubism is considered as a familial/inherited disease but many sporadic cases have been reported in literature with no familial history. Osteoblastic and osteoclastic remodeling replaces normal bone by excessive amount of fibrovascular tissue containing multinucleated giant cells. Here, we present a case report of cherubism in a 10 year old boy describing the clinical, histological, biochemical and radiographic features. äCherubism: A Case Report (epmc).pdf DeepDyve Pubget Overpricing