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10.1093/ckj/sfs004 http://scihub22266oqcxt.onion/10.1093/ckj/sfs004 C5783209!5783209!29497513     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       Clin+Kidney+J 2012 ; 5 (2): 130-2 Nephropedia Template TP {{tp|p=29497513|t=2012. Amyloid proximal tubulopathy: a novel form of light chain proximal tubulopathy |pdf=|usr=}}{{29497513}} gab.com Text Amyloid proximal tubulopathy: a novel form of light chain proximal tubulopathy JO: Clin Kidney J http://www.kidney.de/pget.php?&tw=1&pmid=29497513 #FOAvip Light chain proximal tubulopathy is a paraproteinemic-related kidney disease most commonly seen in patients with a plasma cell dyscrasia. The classic description is that of proximal tubules with kappa-restricted intracytoplasmic crystals in a patient with a clinical Fanconi?s syndrome. Recently, other variants of light chain proximal tubulopathy have been described including those without crystal formation. We expand the morphologic spectrum in this report of a patient who presented with acute renal failure, proteinuria and hematuria. Biopsy revealed proximal tubulopathy in which the proximal tubules show intracytoplasmic amyloid formation. This is the first description, to our knowledge, of amyloid proximal tubulopathy. Twit Text FOAVip Amyloid proximal tubulopathy: a novel form of light chain proximal tubulopathy ????Clin Kidney J http://www.kidney.de/pget.php?&tw=1&pmid=29497513 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=29497513 #FOAvip English Wikipedia <ref>{{Cite pmid|29497513}}</ref> Amyloid proximal tubulopathy: a novel form of light chain proximal tubulopathy #MMPMID29497513 Larsen CP; Borrelli GS; Walker PD Clin Kidney J 2012[Apr]; 5 (2): 130-2 PMID29497513show ga Light chain proximal tubulopathy is a paraproteinemic-related kidney disease most commonly seen in patients with a plasma cell dyscrasia. The classic description is that of proximal tubules with kappa-restricted intracytoplasmic crystals in a patient with a clinical Fanconi?s syndrome. Recently, other variants of light chain proximal tubulopathy have been described including those without crystal formation. We expand the morphologic spectrum in this report of a patient who presented with acute renal failure, proteinuria and hematuria. Biopsy revealed proximal tubulopathy in which the proximal tubules show intracytoplasmic amyloid formation. This is the first description, to our knowledge, of amyloid proximal tubulopathy. äAmyloid proximal tubulopathy: a novel form of light chain proximal tub(epmc).pdf DeepDyve Pubget Overpricing