[Thrombotic microangiopathies]
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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[Thrombotic microangiopathies]. / Nielsen, O.J.; Friis-Hansen, L.
I: Ugeskrift for læger, Bind 171, Nr. 49, 2009, s. 3614-3620.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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TY - JOUR
T1 - [Thrombotic microangiopathies]
AU - Nielsen, O.J.
AU - Friis-Hansen, L.
N1 - Cochrane: Den danske tekst klippet hertil, De trombotiske mikroangiopatier, og den engelske tekst downloadet.
PY - 2009
Y1 - 2009
N2 - The thrombotic microangiopathic diseases, which include acquired and congenital TTP and HUS, are most frequently acute disease entities. Untreated, these diseases are associated with a lethal course in many cases. Deficiency of the von Willebrand cleaving enzyme, ADAMTS13, is a decisive pathophysiological defect in most cases of thrombotic microangiopathic diseases. Early recognition and a secure distinction from other conditions that resemble TMA diseases is essential in order to institute adequate treatment and to obtain a favourable outcome in terms of both survival and development of serious sequelae Udgivelsesdato: 2009/11/30
AB - The thrombotic microangiopathic diseases, which include acquired and congenital TTP and HUS, are most frequently acute disease entities. Untreated, these diseases are associated with a lethal course in many cases. Deficiency of the von Willebrand cleaving enzyme, ADAMTS13, is a decisive pathophysiological defect in most cases of thrombotic microangiopathic diseases. Early recognition and a secure distinction from other conditions that resemble TMA diseases is essential in order to institute adequate treatment and to obtain a favourable outcome in terms of both survival and development of serious sequelae Udgivelsesdato: 2009/11/30
M3 - Tidsskriftartikel
VL - 171
SP - 3614
EP - 3620
JO - Ugeskrift for Laeger
JF - Ugeskrift for Laeger
SN - 0041-5782
IS - 49
ER -
ID: 19797819