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1
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Mutations in complement C3 predispose to development of atypical hemolytic uremic syndrome.
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Blood
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2008
|
3.10
|
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2
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Association of factor H autoantibodies with deletions of CFHR1, CFHR3, CFHR4, and with mutations in CFH, CFI, CD46, and C3 in patients with atypical hemolytic uremic syndrome.
|
Blood
|
2009
|
3.10
|
|
3
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Deletion of complement factor H-related genes CFHR1 and CFHR3 is associated with atypical hemolytic uremic syndrome.
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PLoS Genet
|
2007
|
2.79
|
|
4
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Atypical haemolytic uraemic syndrome associated with a hybrid complement gene.
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PLoS Med
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2006
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2.07
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|
5
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Plasma therapy in atypical haemolytic uremic syndrome: lessons from a family with a factor H mutation.
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Pediatr Nephrol
|
2008
|
1.68
|
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6
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De novo gene conversion in the RCA gene cluster (1q32) causes mutations in complement factor H associated with atypical hemolytic uremic syndrome.
|
Hum Mutat
|
2006
|
1.46
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7
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Maintenance of kidney function following treatment with eculizumab and discontinuation of plasma exchange after a third kidney transplant for atypical hemolytic uremic syndrome associated with a CFH mutation.
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Am J Kidney Dis
|
2009
|
1.39
|
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8
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Posttransplantation cytomegalovirus-induced recurrence of atypical hemolytic uremic syndrome associated with a factor H mutation: successful treatment with intensive plasma exchanges and ganciclovir.
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Am J Kidney Dis
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2005
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1.31
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9
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The complement factor H R1210C mutation is associated with atypical hemolytic uremic syndrome.
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J Am Soc Nephrol
|
2008
|
1.31
|
|
10
|
Prophylactic plasma exchange in CD46-associated atypical haemolytic uremic syndrome.
|
Pediatr Nephrol
|
2009
|
1.16
|
|
11
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A novel hybrid CFH/CFHR3 gene generated by a microhomology-mediated deletion in familial atypical hemolytic uremic syndrome.
|
Blood
|
2011
|
1.09
|
|
12
|
Common genetic variants in complement genes other than CFH, CD46 and the CFHRs are not associated with aHUS.
|
Mol Immunol
|
2011
|
1.06
|
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13
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A novel non-synonymous polymorphism (p.Arg240His) in C4b-binding protein is associated with atypical hemolytic uremic syndrome and leads to impaired alternative pathway cofactor activity.
|
J Immunol
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2008
|
1.03
|
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14
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Complement factor H-associated atypical hemolytic uremic syndrome in monozygotic twins: concordant presentation, discordant response to treatment.
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Am J Kidney Dis
|
2006
|
0.94
|
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15
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Atypical relapse of hemolytic uremic syndrome after transplantation.
|
Pediatr Nephrol
|
2004
|
0.91
|
|
16
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Triggering of atypical hemolytic uremic syndrome by influenza A (H1N1).
|
Ren Fail
|
2010
|
0.90
|
|
17
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Determining the population frequency of the CFHR3/CFHR1 deletion at 1q32.
|
PLoS One
|
2013
|
0.90
|
|
18
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Factor H autoantibodies in membranoproliferative glomerulonephritis.
|
Mol Immunol
|
2012
|
0.89
|
|
19
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Challenges in the management of infantile factor H associated hemolytic uremic syndrome.
|
Pediatr Nephrol
|
2004
|
0.88
|
|
20
|
Is complement factor H a susceptibility factor for IgA nephropathy?
|
Mol Immunol
|
2009
|
0.87
|
|
21
|
Complement factor h autoantibodies and age-related macular degeneration.
|
Invest Ophthalmol Vis Sci
|
2010
|
0.87
|
|
22
|
Association of a factor H mutation with hemolytic uremic syndrome following a diarrheal illness.
|
Am J Kidney Dis
|
2008
|
0.85
|
|
23
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Factor I autoantibodies in patients with atypical hemolytic uremic syndrome: disease-associated or an epiphenomenon?
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Clin J Am Soc Nephrol
|
2012
|
0.84
|
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24
|
Phenotypic variations of cartilage hair hypoplasia: granulomatous skin inflammation and severe T cell immunodeficiency as initial clinical presentation in otherwise well child with short stature.
|
J Clin Immunol
|
2013
|
0.80
|
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25
|
Successful simultaneous liver-kidney transplant in an adult with atypical hemolytic uremic syndrome associated with a mutation in complement factor H.
|
Am J Kidney Dis
|
2011
|
0.79
|
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26
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A case of acute myeloid leukemia with inv(16)(p13q22) reveals a novel MYH11 breakpoint and a new CBF beta-MYH11 transcript variant.
|
Haematologica
|
2007
|
0.76
|