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.

10.1007/s13730-020-00550-1 http://scihub22266oqcxt.onion/10.1007/s13730-020-00550-1 33156494!8019448!33156494     free     free     free       CEN+Case+Rep 2021 ; 10 (2): 236-240 Nephropedia Template TP {{tp|p=33156494|t=2021. First case report of monoclonal IgG3-heavy-chain glomerulonephritis with microtubular structures |pdf=|usr=}}{{33156494}} gab.com Text First case report of monoclonal IgG3-heavy-chain glomerulonephritis with microtubular structures JO: CEN Case Rep http://www.kidney.de/pget.php?&tw=1&pmid=33156494 #FOAvip Our patient was a 69-year-old woman admitted to our hospital for heavy proteinuria and hematuria. A renal biopsy showed findings similar to those of membranoproliferative glomerulonephritis associated with nodular lesions, and immunofluorescence showed marked deposits of IgG, C1q, and C3 on the peripheral capillary walls. IgG3 alone was observed on IgG subclass staining with no kappa or lambda light chains, and Congo red staining was negative. These findings suggested IgG3-heavy-chain deposition disease (HCDD). However, we did not find a deletion of the first heavy-chain constant domain, which is commonly observed in HCDD. Electron microscopy showed randomly arranged subendothelial microtubular structures with diameters of 70-90 nm. Altogether, the diagnosis of HCDD could not be made, although monoclonal IgG3 deposits in glomeruli were observed. This is the first case report of monoclonal IgG3-heavy-chain glomerulonephritis with subendothelial-based, randomly arranged microtubular structures with diameters of 70-90 nm. Twit Text FOAVip First case report of monoclonal IgG3-heavy-chain glomerulonephritis with microtubular structures ????CEN Case Rep http://www.kidney.de/pget.php?&tw=1&pmid=33156494 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=33156494 #FOAvip English Wikipedia <ref>{{Cite pmid|33156494}}</ref> First case report of monoclonal IgG3-heavy-chain glomerulonephritis with microtubular structures #MMPMID33156494 Matsuura Y; Goto T; Tamayama Y; Nakamura Y; Oyama J; Ishioka H; Yoshikawa K; Nakaya I; Soma J CEN Case Rep 2021[May]; 10 (2): 236-240 PMID33156494show ga Our patient was a 69-year-old woman admitted to our hospital for heavy proteinuria and hematuria. A renal biopsy showed findings similar to those of membranoproliferative glomerulonephritis associated with nodular lesions, and immunofluorescence showed marked deposits of IgG, C1q, and C3 on the peripheral capillary walls. IgG3 alone was observed on IgG subclass staining with no kappa or lambda light chains, and Congo red staining was negative. These findings suggested IgG3-heavy-chain deposition disease (HCDD). However, we did not find a deletion of the first heavy-chain constant domain, which is commonly observed in HCDD. Electron microscopy showed randomly arranged subendothelial microtubular structures with diameters of 70-90 nm. Altogether, the diagnosis of HCDD could not be made, although monoclonal IgG3 deposits in glomeruli were observed. This is the first case report of monoclonal IgG3-heavy-chain glomerulonephritis with subendothelial-based, randomly arranged microtubular structures with diameters of 70-90 nm. |Aged[MESH] |Antibodies, Monoclonal/isolation & purification/*ultrastructure[MESH] |Female[MESH] |Glomerulonephritis/*pathology[MESH] |Humans[MESH]First case report of monoclonal IgG3-heavy-chain glomerulonephritis wi(epmc).pdf DeepDyve Pubget Overpricing