Atypical hemolytic uremic syndrome: telling the difference between H and Y.

scientific article

Atypical hemolytic uremic syndrome: telling the difference between H and Y. is …
instance of (P31):
scholarly articleQ13442814

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P6179Dimensions Publication ID1001222351
P356DOI10.1038/KI.2010.222
P698PubMed publication ID20877372

P50authorMatthew C PickeringQ55692581
P2093author name stringE Goicoechea de Jorge
P2860cites workAtypical hemolytic-uremic syndromeQ33386736
Impact of compound heterozygous complement factor H mutations on development of atypical hemolytic uremic syndrome-A pedigree revisitedQ33388816
Variant-specific quantification of factor H in plasma identifies null alleles associated with atypical hemolytic uremic syndromeQ33391370
Genetic and environmental factors influencing the human factor H plasma levelsQ43958315
Deletion of complement factor H-related genes CFHR1 and CFHR3 is associated with atypical hemolytic uremic syndromeQ21145235
The human complement factor H: functional roles, genetic variations and disease associationsQ28263548
Atypical haemolytic uraemic syndrome associated with a hybrid complement geneQ28766922
Insights into hemolytic uremic syndrome: segregation of three independent predisposition factors in a large, multiple affected pedigreeQ33369744
Factor H autoantibodies in atypical hemolytic uremic syndrome correlate with CFHR1/CFHR3 deficiencyQ33377384
Thrombomodulin mutations in atypical hemolytic-uremic syndromeQ33385474
P433issue8
P407language of work or nameEnglishQ1860
P921main subjectatypical hemolytic uremic syndromeQ17165460
P304page(s)721-723
P577publication date2010-10-01
P1433published inKidney InternationalQ6404823
P1476titleAtypical hemolytic uremic syndrome: telling the difference between H and Y.
P478volume78

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cites work (P2860)
Q37522557Complement related kidney diseases: Recurrence after transplantation
Q58120548Complement-mediated renal diseases after kidney transplantation - current diagnostic and therapeutic options in and recurrent diseases
Q61651844Hyperfunctional complement C3 promotes C5-dependent atypical hemolytic uremic syndrome in mice
Q33399520Thrombotic microangiopathy: current knowledge and outcomes with plasma exchange

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