Atypical hemolytic uremic syndrome associated with mutations in complement regulator genes

scientific article

Atypical hemolytic uremic syndrome associated with mutations in complement regulator genes is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1055/S-0030-1262886
P8608Fatcat IDrelease_oic2fnd77rafbg3evdgulitmam
P698PubMed publication ID20865641
P5875ResearchGate publication ID46414893

P50authorVéronique Frémeaux-BacchiQ30003568
Lubka T. RoumeninaQ48324750
P2093author name stringMarina Noris
Moglie Le Quintrec
P433issue6
P921main subjectatypical hemolytic uremic syndromeQ17165460
P304page(s)641-652
P577publication date2010-09-23
P1433published inSeminars in Thrombosis and HemostasisQ15751825
P1476titleAtypical hemolytic uremic syndrome associated with mutations in complement regulator genes
P478volume36

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cites work (P2860)
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Q33405522Complement genes strongly predict recurrence and graft outcome in adult renal transplant recipients with atypical hemolytic and uremic syndrome
Q33410276Comprehensive genetic analysis of complement and coagulation genes in atypical hemolytic uremic syndrome
Q37959890Crosstalk between complement and toll-like receptors
Q64072728Novel MASP-2 inhibitors developed via directed evolution of human TFPI1 are potent lectin pathway inhibitors
Q33425891Partial Complement Factor H Deficiency Associates with C3 Glomerulopathy and Thrombotic Microangiopathy
Q33411571Renal function in normal and disordered pregnancy
Q35611793Secondary focal and segmental glomerulosclerosis associated with single-nucleotide polymorphisms in the genes encoding complement factor H and C3.
Q33433754Self-nonself discrimination by the complement system
Q38850489Targeting the complement cascade: novel treatments coming down the pike.
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Q33427932Thrombotic microangiopathy without renal involvement: two novel mutations in complement-regulator genes
Q39719068Treatment of atypical uraemic syndrome in the era of eculizumab

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