Renal apolipoprotein A-I amyloidosis: a rare and usually ignored cause of hereditary tubulointerstitial nephritis.
Gregorini G, Izzi C, Obici L, Tardanico R, Röcken C, Viola BF, Capistrano M, Donadei S, Biasi L, Scalvini T, Merlini G, Scolari F.
Gregorini G, et al.
J Am Soc Nephrol. 2005 Dec;16(12):3680-6. doi: 10.1681/ASN.2005040382. Epub 2005 Oct 12.
J Am Soc Nephrol. 2005.
PMID: 16221867
The clinical phenotype was mainly characterized by a variable combination of kidney and liver disturbance. The occurrence of renal involvement seemed to be almost universal, although its severity varied greatly ranging from subclinical organ damage to overt, slowly …
The clinical phenotype was mainly characterized by a variable combination of kidney and liver disturbance. The occurrence of renal …