A child with relapsing haemolytic anemia and thrombocytopenia;Et barn med residiverende hemolytisk anemi og trombocytopeni

Tidsskrift for den Norske Laegeforening

Volumn 127, Issue 7, 2007, Pages 884-885

  Gulati, Sasha ^a   Siebke, Elisabeth ^a   Gamlem, Agnete Malm ^b  

^a Barneavdelingen   (Norway)

^b NORWEGIAN UNIVERSITY OF SCIENCE AND TECHNOLOGY   (Norway)

Author keywords

[No Author keywords available]

Indexed keywords

ADAM PROTEIN; ADAMTS13 PROTEIN, HUMAN; UNCLASSIFIED DRUG;

ARTICLE; BLOOD; BLOOD COMPONENT THERAPY; CASE REPORT; DIFFERENTIAL DIAGNOSIS; FEMALE; GENETICS; HUMAN; INFANT; NEWBORN; RECURRENT DISEASE; THROMBOCYTOPENIA; THROMBOTIC THROMBOCYTOPENIC PURPURA;

ADAM PROTEINS; BLOOD COMPONENT TRANSFUSION; DIAGNOSIS, DIFFERENTIAL; FEMALE; HUMANS; INFANT; INFANT, NEWBORN; PURPURA, THROMBOTIC THROMBOCYTOPENIC; RECURRENCE; THROMBOCYTOPENIA;

EID: 34047192953     PISSN: 00292001     EISSN: 08077096     Source Type: Journal    
DOI: None     Document Type: Article

References (10)

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2. Kwaan HC, Soff GA. Management of thrombotic thrombocytopenic purpura and hemolytic uremic syndrome. Semin Hematol 1997; 2: 159-66.
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9. Lester WA, Williams MD, Allford SL et al. Succesful treatment of congenital thrombotic thrombocytopenic purpura using the intermediate purity factor VIII concentrate BPL 8Y. Br J Haematol 2002; 119: 176-9.
10. Allford SL, Harrison P, Lawrie AS et al. Von Willebrand factor-cleaving protease activity in congenital thrombotic thrombocytopenic purpura. Br J Haematol 2000; 111: 1215-22.