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10.1177/0022034514529150 http://scihub22266oqcxt.onion/10.1177/0022034514529150 C4107543!4107543!24700690     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=24700690&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 Deprecated: Implicit conversion from float 231.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 231.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       J+Dent+Res 2014 ; 93 (7 Suppl): 7S-19S Nephropedia Template TP {{tp|p=24700690|t=2014. Rare Bone Diseases and Their Dental, Oral, and Craniofacial Manifestations |pdf=|usr=}}{{24700690}} gab.com Text Rare Bone Diseases and Their Dental, Oral, and Craniofacial Manifestations JO: J Dent Res http://www.kidney.de/pget.php?&tw=1&pmid=24700690 #FOAvip Hereditary diseases affecting the skeleton are heterogeneous in etiology and severity. Though many of these conditions are individually rare, the total number of people affected is great. These disorders often include dental-oral-craniofacial (DOC) manifestations, but the combination of the rarity and lack of in-depth reporting often limit our understanding and ability to diagnose and treat affected individuals. In this review, we focus on dental, oral, and craniofacial manifestations of rare bone diseases. Discussed are defects in 4 key physiologic processes in bone/tooth formation that serve as models for the understanding of other diseases in the skeleton and DOC complex: progenitor cell differentiation (fibrous dysplasia), extracellular matrix production (osteogenesis imperfecta), mineralization (familial tumoral calcinosis/hyperostosis hyperphosphatemia syndrome, hypophosphatemic rickets, and hypophosphatasia), and bone resorption (Gorham-Stout disease). For each condition, we highlight causative mutations (when known), etiopathology in the skeleton and DOC complex, and treatments. By understanding how these 4 foci are subverted to cause disease, we aim to improve the identification of genetic, molecular, and/or biologic causes, diagnoses, and treatment of these and other rare bone conditions that may share underlying mechanisms of disease. Twit Text FOAVip Rare Bone Diseases and Their Dental, Oral, and Craniofacial Manifestations ????J Dent Res http://www.kidney.de/pget.php?&tw=1&pmid=24700690 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=24700690 #FOAvip English Wikipedia <ref>{{Cite pmid|24700690}}</ref> Rare Bone Diseases and Their Dental, Oral, and Craniofacial Manifestations #MMPMID24700690 Foster B; Ramnitz M; Gafni R; Burke A; Boyce A; Lee J; Wright J; Akintoye S; Somerman M; Collins M J Dent Res 2014[Jul]; 93 (7 Suppl): 7S-19S PMID24700690show ga Hereditary diseases affecting the skeleton are heterogeneous in etiology and severity. Though many of these conditions are individually rare, the total number of people affected is great. These disorders often include dental-oral-craniofacial (DOC) manifestations, but the combination of the rarity and lack of in-depth reporting often limit our understanding and ability to diagnose and treat affected individuals. In this review, we focus on dental, oral, and craniofacial manifestations of rare bone diseases. Discussed are defects in 4 key physiologic processes in bone/tooth formation that serve as models for the understanding of other diseases in the skeleton and DOC complex: progenitor cell differentiation (fibrous dysplasia), extracellular matrix production (osteogenesis imperfecta), mineralization (familial tumoral calcinosis/hyperostosis hyperphosphatemia syndrome, hypophosphatemic rickets, and hypophosphatasia), and bone resorption (Gorham-Stout disease). For each condition, we highlight causative mutations (when known), etiopathology in the skeleton and DOC complex, and treatments. By understanding how these 4 foci are subverted to cause disease, we aim to improve the identification of genetic, molecular, and/or biologic causes, diagnoses, and treatment of these and other rare bone conditions that may share underlying mechanisms of disease. äRare Bone Diseases and Their Dental, Oral, and Craniofacial Manifestat(epmc).pdf DeepDyve Pubget Overpricing