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Difficulties and pi...
Difficulties and pitfalls in the laboratory diagnosis of bleeding disorders
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Bolton-Maggs, P. H. B. (författare)
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Favaloro, E. J. (författare)
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- Hillarp, Andreas (författare)
- Lund University,Lunds universitet,Klinisk kemi, Malmö,Forskargrupper vid Lunds universitet,Clinical Chemistry, Malmö,Lund University Research Groups
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Jennings, I. (författare)
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Kohler, H. P. (författare)
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(creator_code:org_t)
- 2012-06-25
- 2012
- Engelska.
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Ingår i: Haemophilia. - : Wiley. - 1351-8216. ; 18, s. 66-72
- Relaterad länk:
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http://dx.doi.org/10...
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https://www.onlineli...
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https://lup.lub.lu.s...
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https://doi.org/10.1...
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Abstract
Ämnesord
Stäng
- . von Willebrand disease (VWD) is the most common inherited bleeding disorder, but variable severity and several classification types mean that diagnosis is often not straightforward. In many countries, the assays are not readily available and/or are not well standardized. The latest methods and the basis of VWD are discussed here, together with information from the international quality assessment programme (IEQAS). Factor XIII deficiency is a rare, but important bleeding disorder, which may be missed or diagnosed late. A discussion and update on this diagnosis is considered in the final section of our review.
Ämnesord
- MEDICIN OCH HÄLSOVETENSKAP -- Klinisk medicin -- Hematologi (hsv//swe)
- MEDICAL AND HEALTH SCIENCES -- Clinical Medicine -- Hematology (hsv//eng)
Nyckelord
- bleeding disorders
- external quality assurance
- factor XIII deficiency
- laboratory diagnosis
- von Willebrand disease
Publikations- och innehållstyp
- art (ämneskategori)
- ref (ämneskategori)
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