scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1001222351 |
P356 | DOI | 10.1038/KI.2010.222 |
P698 | PubMed publication ID | 20877372 |
P50 | author | Matthew C Pickering | Q55692581 |
P2093 | author name string | E Goicoechea de Jorge | |
P2860 | cites work | Atypical hemolytic-uremic syndrome | Q33386736 |
Impact of compound heterozygous complement factor H mutations on development of atypical hemolytic uremic syndrome-A pedigree revisited | Q33388816 | ||
Variant-specific quantification of factor H in plasma identifies null alleles associated with atypical hemolytic uremic syndrome | Q33391370 | ||
Genetic and environmental factors influencing the human factor H plasma levels | Q43958315 | ||
Deletion of complement factor H-related genes CFHR1 and CFHR3 is associated with atypical hemolytic uremic syndrome | Q21145235 | ||
The human complement factor H: functional roles, genetic variations and disease associations | Q28263548 | ||
Atypical haemolytic uraemic syndrome associated with a hybrid complement gene | Q28766922 | ||
Insights into hemolytic uremic syndrome: segregation of three independent predisposition factors in a large, multiple affected pedigree | Q33369744 | ||
Factor H autoantibodies in atypical hemolytic uremic syndrome correlate with CFHR1/CFHR3 deficiency | Q33377384 | ||
Thrombomodulin mutations in atypical hemolytic-uremic syndrome | Q33385474 | ||
P433 | issue | 8 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | atypical hemolytic uremic syndrome | Q17165460 |
P304 | page(s) | 721-723 | |
P577 | publication date | 2010-10-01 | |
P1433 | published in | Kidney International | Q6404823 |
P1476 | title | Atypical hemolytic uremic syndrome: telling the difference between H and Y. | |
P478 | volume | 78 |
Q37522557 | Complement related kidney diseases: Recurrence after transplantation |
Q58120548 | Complement-mediated renal diseases after kidney transplantation - current diagnostic and therapeutic options in and recurrent diseases |
Q61651844 | Hyperfunctional complement C3 promotes C5-dependent atypical hemolytic uremic syndrome in mice |
Q33399520 | Thrombotic microangiopathy: current knowledge and outcomes with plasma exchange |
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