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Clinicopathological analysis of glomerulopathy with fibronectin deposits (GFND): a case of sporadic, elderly-onset GFND with codeposition of IgA, C1q, and fibrinogen.
Yoshino M, Miura N, Ohnishi T, Suzuki K, Kitagawa W, Nishikawa K, Imai H. Yoshino M, et al. Intern Med. 2013;52(15):1715-20. doi: 10.2169/internalmedicine.52.0046. Epub 2012 Mar 1. Intern Med. 2013. PMID: 23903505 Free article. Review.
A 67-year-old Japanese man with recurrent nephrotic syndrome and impaired kidney function had a sporadic, elderly-onset case of glomerulopathy with fibronectin deposits. The daily urinary protein, serum albumin, blood urea nitrogen, and creatinine leve …
A 67-year-old Japanese man with recurrent nephrotic syndrome and impaired kidney function had a sporadic, elderly-onset case of glomerulo …
AJKD Atlas of Renal Pathology: Fibronectin Glomerulopathy.
Lusco MA, Chen YP, Cheng H, Dong HR, Najafian B, Alpers CE, Fogo AB. Lusco MA, et al. Am J Kidney Dis. 2017 Nov;70(5):e21-e22. doi: 10.1053/j.ajkd.2017.09.001. Am J Kidney Dis. 2017. PMID: 29055354 Review. No abstract available.
Molecular genetics of familial hematuric diseases.
Deltas C, Pierides A, Voskarides K. Deltas C, et al. Nephrol Dial Transplant. 2013 Dec;28(12):2946-60. doi: 10.1093/ndt/gft253. Epub 2013 Sep 17. Nephrol Dial Transplant. 2013. PMID: 24046192 Review.
(ii) The FN1 gene, expressed in the glomerulus and responsible for a rare form of glomerulopathy with fibronectin deposits (GFND). (iii) CFHR5 gene, a recently recognized regulator of the complement alternative pathway and mutated in a recently revisit …
(ii) The FN1 gene, expressed in the glomerulus and responsible for a rare form of glomerulopathy with fibronectin de …
An aid to the diagnosis of genetic disorders underlying adult-onset renal failure: a literature review.
Joosten H, Strunk AL, Meijer S, Boers JE, Ariës MJ, Abbes AP, Engel H, Beukhof JR. Joosten H, et al. Clin Nephrol. 2010 Jun;73(6):454-72. doi: 10.5414/cnp73454. Clin Nephrol. 2010. PMID: 20497759 Review.
The following disorders are discussed by mode of inheritance: 1) Autosomal dominant: autosomal dominant polycystic kidney disease, nephropathies associated with uromodulin (medullary cystic disease and familial juvenile hyperuricemic nephropathy), renal cysts and diabetes syndrom …
The following disorders are discussed by mode of inheritance: 1) Autosomal dominant: autosomal dominant polycystic kidney disease, nephropat …