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Volumn 162, Issue 4, 2013, Pages 558-559
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Use of eculizumab in the treatment of a case of refractory, adamts13-deficient thrombotic thrombocytopenic purpura: Additional data and clinical follow-up
c
E DA HOSPITAL
(Taiwan)
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Author keywords
antibodies; atypical haemolytic uraemic syndrome; complement factor h; Thrombotic thrombocytopenic purpura
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Indexed keywords
COMPLEMENT FACTOR H;
COMPLEMENT FACTOR H ANTIBODY;
ECULIZUMAB;
GLUCOCORTICOID;
PROTEIN ANTIBODY;
RITUXIMAB;
UNCLASSIFIED DRUG;
VINCRISTINE;
VON WILLEBRAND FACTOR CLEAVING PROTEINASE;
ANTIBODY DETECTION;
ANTIBODY TITER;
CLINICAL EXAMINATION;
COMPLEMENT FACTOR H GENE;
DRUG APPROVAL;
DRUG MEGADOSE;
ENZYME ACTIVITY;
ENZYME DEFICIENCY;
ENZYME LINKED IMMUNOSORBENT ASSAY;
FOLLOW UP;
GENETIC ANALYSIS;
GENETIC POLYMORPHISM;
HEMATOLOGIC DISEASE;
HUMAN;
KIDNEY DYSFUNCTION;
LETTER;
NEUROLOGIC DISEASE;
OPTICAL DENSITY;
OUTCOME ASSESSMENT;
PLASMAPHERESIS;
PRIORITY JOURNAL;
THERAPY RESISTANCE;
THROMBOCYTE COUNT;
THROMBOCYTOPENIA;
THROMBOTIC THROMBOCYTOPENIC PURPURA;
TREATMENT DURATION;
TREATMENT RESPONSE;
ANTIBODIES;
ATYPICAL HAEMOLYTIC URAEMIC SYNDROME;
COMPLEMENT FACTOR H;
THROMBOTIC THROMBOCYTOPENIC PURPURA;
ANTIBODIES, MONOCLONAL, HUMANIZED;
HUMANS;
MALE;
PURPURA, THROMBOTIC THROMBOCYTOPENIC;
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EID: 84880700770
PISSN: 00071048
EISSN: 13652141
Source Type: Journal
DOI: 10.1111/bjh.12387 Document Type: Letter |
Times cited : (41)
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References (6)
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