Glomerulopathy associated with predominant fibronectin deposits: A newly recognized hereditary disease-Reference-Cited by-同舟云学术

Glomerulopathy associated with predominant fibronectin deposits: A newly recognized hereditary disease

Published:1995-07 Issue:1 Volume:48 Page:163-170
ISSN:0085-2538
Container-title:Kidney International
language:en
Short-container-title:Kidney International

Author:

Strøm Erik H.,Banfi Giovanni,Krapf Reto,Abt Arthur B.,Mazzucco Gianna,Monga Guido,Gloor Friedrich,Neuweiler Jörg,Riess Regine,Stosiek Peter,Hebert Lee A.,Sedmak Daniel D.,Gudat Fred,Mihatsch Michael J.

Publisher

Elsevier BV

Subject

Nephrology

Reference26 articles.

1. Collagen type III glomerulopathy: A new idiopathic glomerular disease;Imbasciati;Am J Nephrol,1991

2. Collagen type III glomerulopathy: A new type of hereditary nephropathy;Gubler;Pediatr Nephrol,1993

3. Familial glomerulopathy with giant fibrillar deposits;Buergin;Virchows Archiv A,1980

4. A unique familial lobular glomerulopathy;Tuttle;Arch Pathol Lab Med,1987

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