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.

10.1093/ndt/gfu090 http://scihub22266oqcxt.onion/10.1093/ndt/gfu090 C4158338!4158338 !25165189     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=25165189 &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 Warning: imagejpeg(C:\Inetpub\vhosts\kidney.de\httpdocs\phplern\25165189 .jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117       Nephrol+Dial+Transplant 2014 ; 29 Suppl 4 (Suppl 4 ): iv87-94 Nephropedia Template TP {{tp|p=25165189 |t=2014. Nephropathic cystinosis: an international consensus document |pdf=|usr=}}{{25165189 }} gab.com Text Nephropathic cystinosis: an international consensus document JO: Nephrol Dial Transplant http://www.kidney.de/pget.php?&tw=1&pmid=25165189 #FOAvip Cystinosis is caused by mutations in the CTNS gene (17p13.2), which encodes for a lysosomal cystine/proton symporter termed cystinosin. It is the most common cause of inherited renal Fanconi syndrome in young children. Because of its rarity, the diagnosis and specific treatment of cystinosis are frequently delayed, which has a significant impact on the overall prognosis. In this document, we have summarized expert opinions on several aspects of the disease to improve knowledge and provide guidance for diagnosis and treatment. Twit Text FOAVip Nephropathic cystinosis: an international consensus document ????Nephrol Dial Transplant http://www.kidney.de/pget.php?&tw=1&pmid=25165189 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=25165189 #FOAvip English Wikipedia <ref>{{Cite pmid|25165189 }}</ref> Nephropathic cystinosis: an international consensus document #MMPMID25165189 Emma F ; Nesterova G ; Langman C ; Labbé A ; Cherqui S ; Goodyer P ; Janssen MC ; Greco M ; Topaloglu R ; Elenberg E ; Dohil R ; Trauner D ; Antignac C ; Cochat P ; Kaskel F ; Servais A ; Wühl E ; Niaudet P ; Van't Hoff W ; Gahl W ; Levtchenko E Nephrol Dial Transplant 2014[Sep]; 29 Suppl 4 (Suppl 4 ): iv87-94 PMID25165189 show ga Cystinosis is caused by mutations in the CTNS gene (17p13.2), which encodes for a lysosomal cystine/proton symporter termed cystinosin. It is the most common cause of inherited renal Fanconi syndrome in young children. Because of its rarity, the diagnosis and specific treatment of cystinosis are frequently delayed, which has a significant impact on the overall prognosis. In this document, we have summarized expert opinions on several aspects of the disease to improve knowledge and provide guidance for diagnosis and treatment. |Child [MESH] |Cystinosis/*diagnosis/genetics/*therapy [MESH] |Fanconi Syndrome/diagnosis/therapy [MESH] |Humans [MESH] |Practice Guidelines as Topic [MESH]Nephropathic cystinosis: an international consensus document (epmc).pdf DeepDyve Pubget Overpricing