Translational mini-review series on complement factor H: therapies of renal diseases associated with complement factor H abnormalities: atypical haemolytic uraemic syndrome and membranoproliferative glomerulonephritis.
Translational mini-review series on complement factor H: therapies of renal diseases associated with complement factor H abnormalities: atypical haemolytic uraemic syndrome and membranoproliferative glomerulonephritis.
复制标题
补体因子 H 转化迷你综述系列：与补体因子 H 异常相关的肾脏疾病的治疗：非典型溶血性尿毒症综合征和膜增生性肾小球肾炎。
DOI：
10.1111/j.1365-2249.2007.03558.x
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发表时间：
2008
影响因子：
4.6
通讯作者：
Remuzzi,G
中科院分区：
文献类型：
--
作者：
Noris,M;Remuzzi,G
SummaryGenetic and acquired abnormalities in complement factor H (CFH) have been associated with two different human renal diseases: haemolytic uraemic syndrome and membrano proliferative glomerulonephritis. The new genetic and pathogenetic findings in these diseases and their clinical implications for the management and cure of patients are reviewed in this paper.
