Thin basement membrane nephropathy: is there genetic predisposition to more severe disease?
暂无分享,去创建一个
[1] E. Boerwinkle,et al. The association of podocin R229Q polymorphism with increased albuminuria or reduced estimated GFR in a large population-based sample of US adults. , 2008, American journal of kidney diseases : the official journal of the National Kidney Foundation.
[2] T. Tabone,et al. The R229Q mutation in NPHS2 may predispose to proteinuria in thin-basement-membrane nephropathy , 2008, Pediatric Nephrology.
[3] K. Voskarides,et al. COL4A3 founder mutations in Greek-Cypriot families with thin basement membrane nephropathy and focal segmental glomerulosclerosis dating from around 18th century. , 2008, Genetic testing.
[4] K. Kyriacou,et al. COL4A3/COL4A4 mutations producing focal segmental glomerulosclerosis and renal failure in thin basement membrane nephropathy. , 2007, Journal of the American Society of Nephrology : JASN.
[5] C. Kashtan. The wages of thin. , 2007, Journal of the American Society of Nephrology : JASN.
[6] F. Cosio,et al. Thin basement membrane nephropathy associated with other glomerular diseases. , 2005, Seminars in nephrology.
[7] C. Kashtan. Familial hematurias: what we know and what we don’t , 2005, Pediatric Nephrology.
[8] P. van Paassen,et al. Signs and symptoms of thin basement membrane nephropathy: a prospective regional study on primary glomerular disease-The Limburg Renal Registry. , 2004, Kidney international.
[9] J. Krieger,et al. NPHS2 R229Q functional variant is associated with microalbuminuria in the general population. , 2004, Kidney international.
[10] J. Savige,et al. Thin basement membrane nephropathy. , 2003, Kidney international.
[11] L. Truong,et al. Thin basement membrane disease with heavy proteinuria or nephrotic syndrome at presentation. , 2000, American journal of kidney diseases : the official journal of the National Kidney Foundation.
[12] P. D. de Leeuw,et al. Thin GBM nephropathy: premature glomerular obsolescence is associated with hypertension and late onset renal failure. , 1997, Kidney international.
[13] H. Smeets,et al. Benign familial hematuria due to mutation of the type IV collagen alpha4 gene. , 1996, The Journal of clinical investigation.
[14] V. Parsons,et al. Abnormally thin glomerular basement membranes associated with hematuria, proteinuria or renal failure in adults. , 1985, American journal of nephrology.