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Volumn 125, Issue 23, 2015, Pages 3525-3526
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Atypical HUS may become a diagnosis of inclusion
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Author keywords
[No Author keywords available]
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Indexed keywords
COMPLEMENT;
COMPLEMENT COMPONENT C5A;
COMPLEMENT FACTOR H;
COMPLEMENT INHIBITOR;
COMPLEMENT MEMBRANE ATTACK COMPLEX;
ECULIZUMAB;
MEMBRANE COFACTOR PROTEIN;
SHIGA TOXIN;
VON WILLEBRAND FACTOR CLEAVING PROTEINASE;
COMPLEMENT ACTIVATION;
COMPLEMENT ALTERNATIVE PATHWAY;
END STAGE RENAL DISEASE;
ESCHERICHIA COLI;
GENE MUTATION;
HEMOLYTIC UREMIC SYNDROME;
HUMAN;
NOTE;
PRIORITY JOURNAL;
THROMBOCYTOPENIA;
THROMBOTIC THROMBOCYTOPENIC PURPURA;
ATYPICAL HEMOLYTIC UREMIC SYNDROME;
BLOOD;
FEMALE;
MALE;
ATYPICAL HEMOLYTIC UREMIC SYNDROME;
FEMALE;
HUMANS;
MALE;
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EID: 84930959416
PISSN: 00064971
EISSN: 15280020
Source Type: Journal
DOI: 10.1182/blood-2015-04-640656 Document Type: Note |
Times cited : (2)
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References (7)
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