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10.1093/ckj/sfs062 http://scihub22266oqcxt.onion/10.1093/ckj/sfs062 26019812!4432403!26019812     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=26019812&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       Clin+Kidney+J 2012 ; 5 (5): 383-9 Nephropedia Template TP {{tp|p=26019812|t=2012. Heavy-chain deposition disease: a morphological, immunofluorescence and ultrastructural assessment |pdf=|usr=}}{{26019812}} gab.com Text Heavy-chain deposition disease: a morphological, immunofluorescence and ultrastructural assessment JO: Clin Kidney J http://www.kidney.de/pget.php?&tw=1&pmid=26019812 #FOAvip Heavy-chain deposition disease (HCDD) is the least common of the monoclonal immunoglobulin deposition diseases with only 24 reported cases in English literature, including the present case. The rarity of this disease merits its documentation. We present a case of HCDD from our archival material, who presented with rapidly progressive renal failure and nephrotic syndrome and was found to have nodular glomerulosclerosis on renal biopsy which on immunofluorescence and electron microscopy confirmed HCDD of immunoglobulin G1 type without any light-chain deposition. We also present an in-depth literature review on HCDD. Twit Text FOAVip Heavy-chain deposition disease: a morphological, immunofluorescence and ultrastructural assessment ????Clin Kidney J http://www.kidney.de/pget.php?&tw=1&pmid=26019812 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26019812 #FOAvip English Wikipedia <ref>{{Cite pmid|26019812}}</ref> Heavy-chain deposition disease: a morphological, immunofluorescence and ultrastructural assessment #MMPMID26019812 Rane S; Rana S; Mudrabettu C; Jha V; Joshi K Clin Kidney J 2012[Oct]; 5 (5): 383-9 PMID26019812show ga Heavy-chain deposition disease (HCDD) is the least common of the monoclonal immunoglobulin deposition diseases with only 24 reported cases in English literature, including the present case. The rarity of this disease merits its documentation. We present a case of HCDD from our archival material, who presented with rapidly progressive renal failure and nephrotic syndrome and was found to have nodular glomerulosclerosis on renal biopsy which on immunofluorescence and electron microscopy confirmed HCDD of immunoglobulin G1 type without any light-chain deposition. We also present an in-depth literature review on HCDD. ?Heavy-chain deposition disease: a morphological, immunofluorescence an(epmc).pdf DeepDyve Pubget Overpricing