Literature DB >> 4470885

The pathology of the kidney in the Alport syndrome.

G S Spear.   

Abstract

The histologic picture in the kidney in Alport syndrome varies (later lesions resemble glomerulonephritis, pyelonephritis, or interstitial nephritis), and the site of the initial renal lesion is uncertain. We have observed marked characteristic ultrastructural changes in the basement membranes of glomerular capillaries, even when few abnormalities were seen in the kidney by light microscopy. Their cause is unknown. There was no significant evidence that immune complexes, fibrin, or viruses were factors in their pathogenesis.

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Year:  1974        PMID: 4470885

Source DB:  PubMed          Journal:  Birth Defects Orig Artic Ser        ISSN: 0547-6844


  4 in total

1.  Injection of amniotic fluid stem cells delays progression of renal fibrosis.

Authors:  Sargis Sedrakyan; Stefano Da Sacco; Anna Milanesi; Liron Shiri; Astgik Petrosyan; Radka Varimezova; David Warburton; Kevin V Lemley; Roger E De Filippo; Laura Perin
Journal:  J Am Soc Nephrol       Date:  2012-02-02       Impact factor: 10.121

2.  Phenotype recognition. Clinicians' contributions to molecular genetics.

Authors:  K D Gardner
Journal:  West J Med       Date:  1992-05

Review 3.  An update on the pathomechanisms and future therapies of Alport syndrome.

Authors:  Damien Noone; Christoph Licht
Journal:  Pediatr Nephrol       Date:  2012-08-18       Impact factor: 3.714

4.  Stage-specific action of matrix metalloproteinases influences progressive hereditary kidney disease.

Authors:  Michael Zeisberg; Mona Khurana; Velidi H Rao; Dominic Cosgrove; Jean-Philippe Rougier; Michelle C Werner; Charles F Shield; Zena Werb; Raghu Kalluri
Journal:  PLoS Med       Date:  2006-03-07       Impact factor: 11.069

  4 in total

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