[Thrombotic microangiopathies]

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Standard

[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

Harvard

Nielsen, OJ & Friis-Hansen, L 2009, '[Thrombotic microangiopathies]', Ugeskrift for læger, bind 171, nr. 49, s. 3614-3620.

APA

Nielsen, O. J., & Friis-Hansen, L. (2009). [Thrombotic microangiopathies]. Ugeskrift for læger, 171(49), 3614-3620.

Vancouver

Nielsen OJ, Friis-Hansen L. [Thrombotic microangiopathies]. Ugeskrift for læger. 2009;171(49):3614-3620.

Author

Nielsen, O.J. ; Friis-Hansen, L. / [Thrombotic microangiopathies]. I: Ugeskrift for læger. 2009 ; Bind 171, Nr. 49. s. 3614-3620.

Bibtex

@article{1b553310626d11df928f000ea68e967b,
title = "[Thrombotic microangiopathies]",
abstract = "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",
author = "O.J. Nielsen and L. Friis-Hansen",
note = "Cochrane: Den danske tekst klippet hertil, De trombotiske mikroangiopatier, og den engelske tekst downloadet.",
year = "2009",
language = "Dansk",
volume = "171",
pages = "3614--3620",
journal = "Ugeskrift for Laeger",
issn = "0041-5782",
publisher = "Almindelige Danske Laegeforening",
number = "49",

}

RIS

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