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Membranous glomerulonephritis

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end-stage kidney disease, or kidney disease severe enough to require dialysis. Because the above medications carry risk, treatment should not be initiated without careful consideration as to risk/benefit profile. Of note, corticosteroids (typically Prednisone) alone are of little benefit. They should be combined with one of the other 5 medications, each of which, along with prednisone, has shown some benefit in slowing down progression of membranous nephropathy. It must be kept in mind, however, that each of the 5 medications also carry their own risks, on top of prednisone.
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Al-Rabadi, L. F.; Caza, T.; Trivin-Avillach, C.; Rodan, A. R.; Andeen, N.; Hayashi, N.; Williams, B.; Revelo, M. P.; Clayton, F.; Abraham, J.; Lin, E.; Liou, W.; Zou, C. J.; Ramkumar, N.; Cummins, T.; Wilkey, D. W.; Kawalit, I.; Herzog, C.; Storey, A.; Edmondson, R.; Sjoberg, R.; Yang, T.; Chien, J.;
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Goumenos DS, Katopodis KP, Passadakis P, Vardaki E, Liakopoulos V, Dafnis E, Stefanidis I, Vargemezis V, Vlachojannis JG, Siamopoulos KC (2007). "Corticosteroids and ciclosporin A in idiopathic membranous nephropathy: higher remission rates of nephrotic syndrome and less adverse reactions than after
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Perhaps the most difficult aspect of membranous glomerulonephritis is deciding which people to treat with immunosuppressive therapy as opposed to simple "background" or anti-proteinuric therapies. A large part of this difficulty is due to a lack of ability to predict which people will progress to
434:(MAC) on the glomerular epithelial cells. This, in turn, stimulates release of proteases and oxidants by the mesangial and epithelial cells, damaging the capillary walls and causing them to become "leaky". In addition, the epithelial cells also seem to secrete an unknown mediator that reduces 239:
receptor are responsible around 60% of cases of membranous nephropathy. Testing for these anti-PLA2R has revolutionised diagnosis and treatment of this disease in antibody positive patients, and tracking titre level over time allows you to predict risk of disease progression and chance of
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Traditional definitions split membranous nephropathy into 'primary/idiopathic' or 'secondary'. It is likely that instead the field will move to novel classification on the basis of the specific autoantigen detected, though given the current lack of clinical assays (other than for PLA2R
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comparing treatments of membranous nephropathy showed that regimes comprising chlorambucil or cyclophosphamide, either alone or with steroids, were more effective than symptomatic treatment or treatment with steroids alone in inducing remission of the nephrotic syndrome.
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NELL-1 likely the second most common autoantibody with prevalence in MN of 5-10%. It has a heterogenous pattern of secondary association, from none to sarcoidosis, malignancy, drugs such as bucillamine, and infections. Like PLA2R, antibody titres go into remission with
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In 2014, a second autoantigen was discovered, the thrombospondin type 1 domain-containing 7A (THSD7A) system that might account for an additional 1% of membranous nephropathy cases, and appears to be associated with malignancies.
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Sethi, Sanjeev; Debiec, Hanna; Madden, Benjamin; Charlesworth, M. Cristine; Morelle, Johann; Gross, LouAnn; Ravindran, Aishwarya; Buob, David; Jadoul, Michel; Fervenza, Fernando C.; Ronco, Pierre (2020-01-01).
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Sethi, Sanjeev; Madden, Benjamin J.; Debiec, Hanna; Charlesworth, M. Cristine; Gross, LouAnn; Ravindran, Aishwarya; Hummel, Amber M.; Specks, Ulrich; Fervenza, Fernando C.; Ronco, Pierre (2019-06-01).
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Tomas NM, Beck LH, Meyer-Schwesinger C, Seitz-Polski B, Ma H, Zahner G, Dolla G, Hoxha E, Helmchen U, Dabert-Gay AS, Debayle D, Merchant M, Klein J, Salant DJ, Stahl RA, Lambeau G (December 2014).
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Semaphorin3B predominates in children, esp <2 years old. there can be a family history of MN in these patients, it frequently causes progressive disease and it can recur in kidney transplants.
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We include the traditional list of secondary causes, though as above nomenclature is moving towards an autoantibody specific approach. Membranous nephropathy is associated with the following:
654:(in which inflammation is implied, but the glomerulus not explicitly mentioned) is less common, but the phrase is occasionally encountered. These conditions are usually considered together. 247:
Further studies have identidied more novel auto-antigens responsible for causing a membranous nephropathy pattern of injury continue to be published, with antibodies discovered against:
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Treatment of secondary membranous nephropathy is guided by the treatment of the original disease. For treatment of idiopathic membranous nephropathy, the treatment options include
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Hallegua D, Wallace DJ, Metzger AL, Rinaldi RZ, Klinenberg JR (2016). "Cyclosporine for lupus membranous nephritis: experience with ten patients and review of the literature".
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The twin aims of treating membranous nephropathy are first to induce a remission of the nephrotic syndrome and second to prevent the development of end-stage kidney failure. A
200:, though given the very high specificity of anti-PLA2R antibody positivity this can sometimes be avoided in patients with nephrotic syndrome and preserved kidney function 1943: 264:
Protocadherin 7 (PCDH7) in 2020. It is generally described in older patients, who have less complement on renal biopsy and frequently have spontaneous remission.
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EXT1/EXT2 was reported in 2019. It is predominantly found in younger, female patients, and indeed 1/3 of patients with class V lupus nephritis are EXT positive
2082: 460:. Membranous nephropathy in particular is known to increase this risk more than other causes of nephrotic syndrome though the reason for this is not yet clear. 1874: 1938: 753:
Bobart, Shane A.; Vriese, An S. De; Pawar, Aditya S.; Zand, Ladan; Sethi, Sanjeev; Giesen, Callen; Lieske, John C.; Fervenza, Fernando C. (2019-02-01).
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Ziakas PD, Giannouli S, Psimenou E, Nakopoulou L, Voulgarelis M (July 2004). "Membranous glomerulonephritis in chronic lymphocytic leukemia".
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Membranous glomerulopathy, membranous nephritis, (epi)membranous nephropathy, extramembranous glomerulopathy, and perimembranous nephropathy.
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Immune complexes (black) are deposited in a thickened basement membrane creating a "spike and dome" appearance on electron microscopy.
149: 2072: 1867: 491:, subepithelial deposits that nestle against the glomerular basement membrane seems to be the cause of the thickening. Also, the 1521:
Passerini P, Ponticelli C (July 2003). "Corticosteroids, cyclophosphamide, and chlorambucil therapy of membranous nephropathy".
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has a similar name, but is considered a separate condition with a distinctly different causality. Membranoproliferative
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microscopy will reveal typical granular deposition of immunoglobulins and complement along the basement membrane.
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The immune complex serves as an activator that triggers a response from the C5b - C9 complements, which form a
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Within membranous glomerulonephritis, especially in cases caused by viral hepatitis, serum C3 levels are low.
427:. The antigens may be part of the basement membrane, or deposited from elsewhere by the systemic circulation. 1372:"Segmental membranous glomerulonephritis in children: comparison with global membranous glomerulonephritis" 2128: 1910: 449: 423:
formation in the glomerulus. The immune complexes are formed by binding of antibodies to antigens in the
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Markowitz GS (May 2001). "Membranous glomerulopathy: emphasis on secondary forms and disease variants".
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Although it usually affects the entire glomerulus, it can affect parts of the glomerulus in some cases.
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The defining point of MGN is the presence of subepithelial immunoglobulin-containing deposits along the
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About a third of untreated patients have spontaneous remission, another third progress to require
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von Groote TC, Williams G, Au EH, Chen Y, Mathew AT, Hodson EM, Tunnicliffe DJ (November 2021).
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spontaneous remission There is little secondary disease association with PLA2R autoantibodies.
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are often also present. Others may not have symptoms and may be picked up on screening, with
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Obana M, Nakanishi K, Sako M, Yata N, Nozu K, Tanaka R, Iijima K, Yoshikawa N (July 2006).
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Logt, Anne-Els van de; Fresquet, Maryline; Wetzels, Jack F.; Brenchley, Paul (2019-12-01).
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NDNF is associated with syphilis (close to 100% of membranous nephrology is NDNF positive).
2050: 2038: 1775: 952:"Neural epidermal growth factor-like 1 protein (NELL-1) associated membranous nephropathy" 620: 553: 736: 481: 62: 1883: 1454: 1429: 1327: 1302: 1143: 1118: 1082: 1025: 1000: 926: 901: 828: 640: 624: 557: 541: 420: 177: 1686: 1534: 17: 2122: 1569: 603: 526: 358: 346: 1628: 1585: 1303:"Membranous nephropathy in children: clinical presentation and therapeutic approach" 1287: 269:
FAT1 is associated with haemopoetic stem cell transplant, and responds to treatment
2064: 1852: 1507: 1445: 1119:"Serine Protease HTRA1 as a Novel Target Antigen in Primary Membranous Nephropathy" 644: 572: 567: 496: 395: 115: 103: 1732: 1697: 1049: 902:"Thrombospondin type-1 domain-containing 7A in idiopathic membranous nephropathy" 452:), membranous nephropathy is known to predispose affected individuals to develop 270: 265: 61:
of membranous nephropathy showing prominent glomerular basement membrane spikes.
803: 707: 636: 561: 391: 354: 322: 318: 256: 193: 165: 111: 1612: 968: 869: 771: 258:. Prognosis is good. A less common target antigen in lupus nephritis is NCAM1. 1708: 1318: 695: 691: 577: 453: 350: 292: 222: 189: 75: 58: 1073: 977: 878: 780: 1727: 1670: 741: 670: 651: 592: 362: 338: 305: 1620: 1577: 1542: 1499: 1463: 1397: 1336: 1279: 1152: 1134: 1105:
https://www.kidney-international.org/article/S0085-2538(20)31180-7/fulltext
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Merchant, M.; Arthur, J.; Klein, J.; Larsen, C.; Beck Jr, L. H. (2021).
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and the last third continue to have proteinuria, without progression of
500: 435: 314: 173: 1491: 1271: 1665: 480:, the basement membrane is observed to be diffusely thickened. Using 342: 197: 196:. A definitive diagnosis of membranous nephropathy requires a kidney 107: 99: 643:
both refer to a similar constellation but without the assumption of
1744: 410: 386: 169: 120: 694:; Cohen, Arthur H.; Jennette, J. Charles; Bruijn, Jan A. (eds.), 536:
Recommended first line immunosuppressive therapy often includes:
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affecting mostly people between ages of 30 and 50 years, usually
375: 333: 1856: 1748: 326: 225:(of unknown origin or cause). This can also be referred to as 1050:"Exostosin 1/Exostosin 2–Associated Membranous Nephropathy" 484:, the GBM appears to have a "spiked" or "holey" appearance. 525:
drugs and non-specific anti-proteinuric measures such as
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Clinical Journal of the American Society of Nephrology
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Similar to other causes of nephrotic syndrome (e.g.,
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autoantibodies) this may be several years off still.
1643: 2095: 2059: 2020: 1998: 1982: 1957: 1929: 1901: 1890: 1718: 1647: 69: 40: 35: 398:; melanomas; hematological malignancies such as 217:Traditionally 85% of MGN cases are classified as 2083:Eosinophilic granulomatosis with polyangiitis 1868: 1760: 1478:traditional treatment with cytotoxic drugs". 1123:Journal of the American Society of Nephrology 1054:Journal of the American Society of Nephrology 808:Journal of the American Society of Nephrology 221:—that is to say, the cause of the disease is 8: 1434:The Cochrane Database of Systematic Reviews 1995: 1898: 1875: 1861: 1853: 1767: 1753: 1745: 1644: 804:"New 'Antigens' in Membranous Nephropathy" 702:, New York, NY: Springer, pp. 21–29, 152:(FSGS) recently becoming the most common. 80: 49: 32: 1453: 1387: 1326: 1142: 1081: 1024: 967: 925: 868: 827: 770: 194:high amounts of protein loss in the urine 98:) is a slowly progressive disease of the 659:membranoproliferative glomerulonephritis 1949:Membranoproliferative/mesangiocapillary 1801:Mesangial proliferative lupus nephritis 682: 544:, also known as the Ponticelli regime. 144:It is the second most common cause of 1301:Menon S, Valentini RP (August 2010). 635:The closely related terms membranous 219:primary membranous glomerulonephritis 7: 1791:Minimal mesangial glomerulonephritis 906:The New England Journal of Medicine 446:focal segmental glomerulosclerosis 150:focal segmental glomerulosclerosis 25: 548:Immunosuppressive therapy options 390:, frequently solid tumors of the 227:idiopathic membranous nephropathy 2073:Granulomatosis with polyangiitis 1884:Disease of the kidney glomerules 1570:10.1097/00125480-200105000-00001 531:angiotensin II receptor blockers 1821:Diffuse proliferative nephritis 700:Fundamentals of Renal Pathology 1558:Advances in Anatomic Pathology 1480:American Journal of Nephrology 1446:10.1002/14651858.CD004293.pub4 1260:American Journal of Hematology 278:HTRA1, often in older persons. 92:Membranous glomerulonephritis 1: 1811:Focal proliferative nephritis 1535:10.1016/S0270-9295(03)00052-4 737:Membranous Glomerulonephritis 36:Membranous glomerulonephritis 1001:"The Many Faces of NELL1 MN" 608:randomized controlled trials 470:glomerular basement membrane 438:synthesis and distribution. 425:glomerular basement membrane 400:chronic lymphocytic leukemia 299:systemic lupus erythematosus 160:Most people will present as 1944:Endocapillary proliferative 708:10.1007/978-0-387-31127-2_2 696:"Membranous Glomerulopathy" 2150: 1613:10.1191/096120300680198935 969:10.1016/j.kint.2019.09.014 870:10.1016/j.kint.2019.07.014 772:10.1016/j.kint.2018.10.021 2026:Type III hypersensitivity 1782: 1319:10.1007/s00467-009-1324-5 57: 48: 2078:Microscopic polyangiitis 2004:Type II hypersensitivity 232:Antibodies to an M-type 1939:Mesangial proliferative 1005:Clinical Kidney Journal 999:Sethi, Sanjeev (2022). 802:Sethi, Sanjeev (2021). 690:Bruijn, Jan A. (2007), 560:without improvement in 432:membrane attack complex 1523:Seminars in Nephrology 1135:10.1681/ASN.2020101395 1066:10.1681/ASN.2018080852 820:10.1681/ASN.2020071082 450:minimal change disease 416: 141: 18:Membranous nephropathy 2044:diffuse proliferative 1412:"KDIGO GN guidelines" 918:10.1056/NEJMoa1409354 588:Mycophenolate mofetil 414: 139: 2012:Goodpasture syndrome 1831:Membranous nephritis 1389:10.2215/CJN.01211005 1307:Pediatric Nephrology 956:Kidney International 857:Kidney International 759:Kidney International 639:(MN) and membranous 164:, with the triad of 1017:10.1093/ckj/sfac237 540:alternating with a 489:electron microscopy 182:High blood pressure 2108:glomerulonephrosis 2103:glomerulonephritis 2034:Post-streptococcal 1841:Glomerulosclerosis 1719:External resources 663:glomerulonephritis 507:Immunofluorescence 417: 213:Primary/idiopathic 162:nephrotic syndrome 156:Signs and symptoms 146:nephrotic syndrome 142: 2116: 2115: 2091: 2090: 1978: 1977: 1903:Non-proliferative 1850: 1849: 1742: 1741: 1492:10.1159/000101367 1351:"Renal Pathology" 1272:10.1002/ajh.20109 1167:"Renal Pathology" 912:(24): 2277–2287. 717:978-0-387-31127-2 667:basement membrane 523:immunosuppressive 419:MGN is caused by 176:(with or without 140:Video explanation 137: 89: 88: 30:Medical condition 16:(Redirected from 2141: 1996: 1899: 1877: 1870: 1863: 1854: 1769: 1762: 1755: 1746: 1645: 1633: 1632: 1596: 1590: 1589: 1553: 1547: 1546: 1518: 1512: 1511: 1474: 1468: 1467: 1457: 1440:(11): CD004293. 1425: 1419: 1418: 1416: 1408: 1402: 1401: 1391: 1367: 1361: 1360: 1358: 1357: 1347: 1341: 1340: 1330: 1298: 1292: 1291: 1255: 1249: 1248: 1246: 1245: 1239:www.uptodate.com 1231: 1225: 1224: 1222: 1221: 1215:www.uptodate.com 1207: 1201: 1200: 1198: 1197: 1191:www.uptodate.com 1183: 1177: 1176: 1174: 1173: 1163: 1157: 1156: 1146: 1129:(7): 1666–1681. 1113: 1107: 1102: 1096: 1095: 1085: 1060:(6): 1123–1136. 1045: 1039: 1038: 1028: 996: 990: 989: 971: 946: 940: 939: 929: 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657:By contrast, 655: 653: 648: 646: 642: 638: 630: 628: 626: 622: 614: 612: 609: 605: 604:meta-analysis 600: 594: 591: 589: 586: 584: 581: 579: 576: 574: 571: 569: 566: 563: 559: 555: 552: 551: 547: 545: 543: 539: 534: 532: 528: 524: 516: 514: 508: 505: 502: 498: 494: 490: 486: 483: 479: 475: 474: 473: 471: 463: 461: 459: 455: 451: 447: 442: 439: 437: 433: 428: 426: 422: 413: 406: 401: 397: 393: 389: 388: 384: 381: 377: 373: 372: 367: 364: 360: 356: 352: 348: 347:penicillamine 344: 340: 336: 335: 331: 328: 324: 320: 316: 312: 308: 307: 303: 300: 296: 294: 290: 289: 288: 282: 277: 274: 271: 268: 266: 263: 260: 257: 254: 250: 249: 248: 245: 241: 238: 230: 228: 224: 220: 212: 210: 203: 201: 199: 195: 191: 187: 183: 179: 175: 171: 167: 163: 155: 153: 151: 147: 119: 117: 116:North African 113: 109: 105: 101: 97: 93: 83: 77: 74: 72: 68: 64: 60: 56: 52: 47: 43: 39: 34: 19: 2065:Pauci-immune 2061:Type III RPG 1958:By condition 1920: 1830: 1826: 1726: 1702: 1691: 1676: 1660: 1604: 1600: 1594: 1561: 1557: 1551: 1526: 1522: 1516: 1483: 1479: 1472: 1437: 1433: 1423: 1406: 1382:(4): 723–9. 1379: 1375: 1365: 1354:. Retrieved 1345: 1310: 1306: 1296: 1266:(3): 271–4. 1263: 1259: 1253: 1242:. Retrieved 1238: 1229: 1218:. Retrieved 1214: 1205: 1194:. Retrieved 1190: 1181: 1170:. Retrieved 1161: 1126: 1122: 1111: 1100: 1057: 1053: 1043: 1008: 1004: 994: 959: 955: 944: 909: 905: 895: 860: 856: 846: 811: 807: 797: 762: 758: 748: 735: 731: 721:, retrieved 699: 685: 656: 649: 645:inflammation 634: 618: 601: 597: 573:Cyclosporine 568:Chlorambucil 535: 520: 512: 482:Jones' stain 467: 443: 440: 429: 418: 407:Pathogenesis 385: 368: 332: 304: 291: 286: 246: 242: 231: 226: 218: 216: 207: 159: 143: 118:ancestry.). 104:white people 95: 91: 90: 63:Jones' stain 2022:Type II RPG 1970:Amyloidosis 650:Membranous 637:nephropathy 631:Terminology 562:proteinuria 495:lose their 454:blood clots 355:Bucillamine 323:hepatitis C 319:hepatitis B 166:albuminuria 41:Other names 2123:Categories 2000:Type I RPG 1921:Membranous 1704:DiseasesDB 1356:2008-11-25 1244:2019-05-11 1235:"UpToDate" 1220:2019-05-11 1211:"UpToDate" 1196:2019-05-11 1187:"UpToDate" 1172:2008-11-25 723:2021-05-16 677:References 578:Tacrolimus 501:hyalinized 464:Morphology 369:inorganic 351:probenecid 306:infections 295:conditions 293:autoimmune 252:treatment. 223:idiopathic 190:urinalysis 76:Nephrology 59:Micrograph 1986:nephritic 1983:Primarily 1894:nephrotic 1891:Primarily 1807:Class III 1728:eMedicine 1074:1046-6673 978:0085-2538 879:0085-2538 781:0085-2538 742:eMedicine 671:mesangium 652:nephritis 615:Prognosis 593:Rituximab 517:Treatment 493:podocytes 363:Tiopronin 361:therapy, 339:captopril 283:Secondary 71:Specialty 1965:Diabetic 1837:Class VI 1817:Class IV 1797:Class II 1629:20048968 1621:10866094 1586:39640332 1578:11345236 1543:12923723 1500:17389782 1464:34778952 1398:17699279 1337:19908069 1288:35937418 1280:15224365 1153:33952630 1092:31061139 1035:36865014 986:31901340 936:25394321 887:31611068 838:33380523 789:30665573 621:dialysis 606:of four 456:such as 359:Anti-TNF 311:syphilis 192:finding 108:European 2096:General 1827:Class V 1787:Class I 1733:med/885 1698:D015433 1508:1475371 1455:8591447 1328:2887508 1144:8425645 1083:6551791 1026:9972807 927:4278759 829:8054892 472:(GBM). 436:nephrin 380:mercury 337:(e.g., 315:malaria 309:(e.g., 297:(e.g., 174:albumin 1627:  1619:  1584:  1576:  1541:  1506:  1498:  1462:  1452:  1396:  1335:  1325:  1286:  1278:  1151:  1141:  1090:  1080:  1072:  1033:  1023:  984:  976:  934:  924:  885:  877:  836:  826:  787:  779:  714:  387:tumors 374:(e.g. 343:NSAIDs 204:Causes 198:biopsy 100:kidney 78:  2039:Lupus 1687:583.1 1625:S2CID 1601:Lupus 1582:S2CID 1504:S2CID 1415:(PDF) 1284:S2CID 396:colon 371:salts 334:drugs 170:edema 114:, or 1709:7970 1693:MeSH 1682:9-CM 1617:PMID 1574:PMID 1539:PMID 1496:PMID 1460:PMID 1438:2021 1394:PMID 1333:PMID 1276:PMID 1149:PMID 1088:PMID 1070:ISSN 1031:PMID 982:PMID 974:ISSN 932:PMID 883:PMID 875:ISSN 834:PMID 785:PMID 777:ISSN 712:ISBN 669:and 394:and 392:lung 376:gold 184:and 180:). 2051:IgA 1991:RPG 1678:ICD 1671:N03 1662:ICD 1609:doi 1566:doi 1531:doi 1488:doi 1450:PMC 1442:doi 1384:doi 1323:PMC 1315:doi 1268:doi 1139:PMC 1131:doi 1078:PMC 1062:doi 1021:PMC 1013:doi 964:doi 922:PMC 914:doi 910:371 865:doi 824:PMC 816:doi 767:doi 740:at 704:doi 529:or 487:On 476:By 448:or 327:HIV 229:. 96:MGN 2125:: 1731:: 1707:: 1696:: 1685:: 1673:.2 1669:: 1666:10 1623:. 1615:. 1603:. 1580:. 1572:. 1560:. 1537:. 1527:23 1525:. 1502:. 1494:. 1484:27 1482:. 1458:. 1448:. 1436:. 1432:. 1392:. 1378:. 1374:. 1331:. 1321:. 1311:25 1309:. 1305:. 1282:. 1274:. 1264:76 1262:. 1237:. 1213:. 1189:. 1147:. 1137:. 1127:32 1125:. 1121:. 1086:. 1076:. 1068:. 1058:30 1056:. 1052:. 1029:. 1019:. 1009:16 1007:. 1003:. 980:. 972:. 960:97 958:. 954:. 930:. 920:. 908:. 904:. 881:. 873:. 861:96 859:. 855:. 832:. 822:. 812:32 810:. 806:. 783:. 775:. 763:95 761:. 757:. 710:, 698:, 647:. 627:. 382:). 378:, 365:). 357:, 353:, 349:, 345:, 341:, 329:). 325:, 321:, 317:, 313:, 301:). 168:, 110:, 2063:/ 2024:/ 2002:/ 1988:, 1876:e 1869:t 1862:v 1843:) 1839:( 1833:) 1829:( 1823:) 1819:( 1813:) 1809:( 1803:) 1799:( 1793:) 1789:( 1768:e 1761:t 1754:v 1680:- 1664:- 1654:D 1631:. 1611:: 1605:9 1588:. 1568:: 1562:8 1545:. 1533:: 1510:. 1490:: 1466:. 1444:: 1417:. 1400:. 1386:: 1380:1 1359:. 1339:. 1317:: 1290:. 1270:: 1247:. 1223:. 1199:. 1175:. 1155:. 1133:: 1094:. 1064:: 1037:. 1015:: 988:. 966:: 938:. 916:: 889:. 867:: 840:. 818:: 791:. 769:: 706:: 564:. 503:. 272:. 236:2 94:( 65:. 20:)

Index

Membranous nephropathy

Micrograph
Jones' stain
Specialty
Nephrology
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kidney
white people
European
Middle Eastern
North African
nephrotic syndrome
focal segmental glomerulosclerosis
nephrotic syndrome
albuminuria
edema
albumin
kidney failure
High blood pressure
high cholesterol
urinalysis
high amounts of protein loss in the urine
biopsy
idiopathic
phospholipase A2



autoimmune

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