Clinico-pathological correlations in 127 patients in 11 large pedigrees, segregating one of three heterozygous mutations in the COL4A3/ COL4A4 genes associated with familial haematuria and significant late progression to proteinuria and chronic kidney disease from focal segmental glomerulosclerosis

Author:

Pierides Alkis,Voskarides Konstantinos,Athanasiou Yiannis,Ioannou Kyriacos,Damianou Loukas,Arsali Maria,Zavros Michalis,Pierides Michael,Vargemezis Vasilios,Patsias Charalambos,Zouvani Ioanna,Elia Avraam,Kyriacou Kyriacos,Deltas Constantinos

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

Reference58 articles.

1. Hereditary familial congenital haemorrhagic nephritis;Alport;Brit Med J,1927

2. Disorders of the basement membrane: hereditary nephritis;Flinter,1998

3. Characteristic ultrastructural lesion of the glomerular basement membrane in progressive hereditary nephritis (Alport syndrome);Hinglais;Lab Invest,1972

4. Alport's syndrome. Emphasizing electron microscopic studies of the glomerulus;Spear;Am J Pathol,1972

5. Pathology of hereditary nephritis;Churg;Arch Path,1973

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