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

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3