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10.1007/s13730-017-0262-5 http://scihub22266oqcxt.onion/10.1007/s13730-017-0262-5 C5694400!5694400!28593486     free     free     free Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       CEN+Case+Rep 2017 ; 6 (2): 148-51 Nephropedia Template TP {{tp|p=28593486|t=2017. Urinary mulberry cells and mulberry bodies are useful tool to detect late-onset Fabry disease |pdf=|usr=}}{{28593486}} gab.com Text Urinary mulberry cells and mulberry bodies are useful tool to detect late-onset Fabry disease JO: CEN Case Rep http://www.kidney.de/pget.php?&tw=1&pmid=28593486 #FOAvip Fabry disease is an X-linked lysosomal storage disorder caused by a lack of ?-galactosidase A activity, which leads to the accumulation of globotriaosylceramide in various organs. A complete lack of ?-galactosidase A activity in a hemizygous male is the classical phenotype, and some hemizygous males show primarily cardiac and/or renal symptoms that appear in adulthood; this is called the variant type or the late-onset type. The kidney and heart are the major target organs, with damage to these organs related to mortality. Thus, in Fabry patients, early detection and early treatment are critical to longevity. Here, we present a 55-year-old Japanese male patient who was diagnosed with late-onset Fabry nephropathy with cardiomyopathy but with no abnormal urinary findings except for urinary mulberry cells and mulberry bodies. In spite of the absence of abnormal urinary findings, the light microscopic and electron microscopic pathological findings showed extensive deposition of globotriaosylceramide to podocytes. In this paper, we propose that the presence of mulberry cells and mulberry bodies can be used for the earlier detection of Fabry nephropathy, especially the late-onset type. Twit Text FOAVip Urinary mulberry cells and mulberry bodies are useful tool to detect late-onset Fabry disease ????CEN Case Rep http://www.kidney.de/pget.php?&tw=1&pmid=28593486 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=28593486 #FOAvip English Wikipedia <ref>{{Cite pmid|28593486}}</ref> Urinary mulberry cells and mulberry bodies are useful tool to detect late-onset Fabry disease #MMPMID28593486 Shimohata H; Maruyama H; Miyamoto Y; Takayasu M; Hirayama K; Kobayashi M CEN Case Rep 2017[Nov]; 6 (2): 148-51 PMID28593486show ga Fabry disease is an X-linked lysosomal storage disorder caused by a lack of ?-galactosidase A activity, which leads to the accumulation of globotriaosylceramide in various organs. A complete lack of ?-galactosidase A activity in a hemizygous male is the classical phenotype, and some hemizygous males show primarily cardiac and/or renal symptoms that appear in adulthood; this is called the variant type or the late-onset type. The kidney and heart are the major target organs, with damage to these organs related to mortality. Thus, in Fabry patients, early detection and early treatment are critical to longevity. Here, we present a 55-year-old Japanese male patient who was diagnosed with late-onset Fabry nephropathy with cardiomyopathy but with no abnormal urinary findings except for urinary mulberry cells and mulberry bodies. In spite of the absence of abnormal urinary findings, the light microscopic and electron microscopic pathological findings showed extensive deposition of globotriaosylceramide to podocytes. In this paper, we propose that the presence of mulberry cells and mulberry bodies can be used for the earlier detection of Fabry nephropathy, especially the late-onset type. äUrinary mulberry cells and mulberry bodies are useful tool to detect l(epmc).pdf DeepDyve Pubget Overpricing