Factor H deficiency and fibrillary glomerulopathy
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Abstract
References (11)
Uncontrolled C3 activation causes membranoproliferative glomerulonephritis in mice deficient in complement factor H
2002 • 495 citations
The Molecular Basis of Familial Hemolytic Uremic Syndrome
2001 • 291 citations
H deficiency in two brothers with atypical dense intramembranous deposit disease
1986 • 173 citations
Factor H and disease: a complement regulator affects vital body functions
1999 • 101 citations
Long-term effects of cyclosporine A in Alport's syndrome
1999 • 96 citations
Factor H and the pathogenesis of renal diseases
2000 • 94 citations
Inherited factor H deficiency and collagen type III glomerulopathy
1995 • 86 citations
Cyclosporine A Slows the Progressive Renal Disease of Alport Syndrome (X-Linked Hereditary Nephritis)
2003 • 86 citations
Hypocomplementemic autosomal recessive hemolytic uremic syndrome with decreased factor H
1998 • 85 citations
Familial relapsing haemolytic uraemic syndrome and complement factor H deficiency
1999 • 66 citations
A familial deficiency of complement factor H
1987 • 47 citations
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