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The problem of diagnosing von Willebrand's disease
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| Zeitschriftentitel: | Journal of Internal Medicine |
|---|---|
| Personen und Körperschaften: | , , , |
| In: | Journal of Internal Medicine, 242, 1997, S740, S. 121-128 |
| Format: | E-Article |
| Sprache: | Englisch |
| veröffentlicht: |
Wiley
|
| Schlagwörter: |
| author_facet |
BATLLE, J. TOREA, J. RENDAL, E. FERNÁNDEZ, M.F.L. BATLLE, J. TOREA, J. RENDAL, E. FERNÁNDEZ, M.F.L. |
|---|---|
| author |
BATLLE, J. TOREA, J. RENDAL, E. FERNÁNDEZ, M.F.L. |
| spellingShingle |
BATLLE, J. TOREA, J. RENDAL, E. FERNÁNDEZ, M.F.L. Journal of Internal Medicine The problem of diagnosing von Willebrand's disease Internal Medicine |
| author_sort |
batlle, j. |
| spelling |
BATLLE, J. TOREA, J. RENDAL, E. FERNÁNDEZ, M.F.L. 0954-6820 1365-2796 Wiley Internal Medicine http://dx.doi.org/10.1111/joim.1997.242.s740.121 <jats:p>Diagnosis of von Willebrand's disease (vWD), particularly vWD Type 1. remains a clinical problem for several aspects. Its definitive diagnosis requires documentation of three factors: bleeding, low levels of qualitively normal von Willebrand factor (vWF), and inheritance. In the absence of any of these factors the diagnosis may be only merely ‘possible’, or even unacceptable. Laboratory diagnosis of vWD includes screening tests and confirmatory tests. vWD Types 2 and 3 are relatively easy to diagnose and appear to be genetic disease of a single locus, the vWF gene. As new genetic and possibly non‐genetic factors are discovered, the diagnosis of vWD Type 1 may become easier.</jats:p> The problem of diagnosing von Willebrand's disease Journal of Internal Medicine |
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Wiley, 1997 |
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Journal of Internal Medicine |
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| title |
The problem of diagnosing von Willebrand's disease |
| title_unstemmed |
The problem of diagnosing von Willebrand's disease |
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The problem of diagnosing von Willebrand's disease |
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The problem of diagnosing von Willebrand's disease |
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The problem of diagnosing von Willebrand's disease |
| title_short |
The problem of diagnosing von Willebrand's disease |
| title_sort |
the problem of diagnosing von willebrand's disease |
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Internal Medicine |
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http://dx.doi.org/10.1111/joim.1997.242.s740.121 |
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1997 |
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121-128 |
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<jats:p>Diagnosis of von Willebrand's disease (vWD), particularly vWD Type 1. remains a clinical problem for several aspects. Its definitive diagnosis requires documentation of three factors: bleeding, low levels of qualitively normal von Willebrand factor (vWF), and inheritance. In the absence of any of these factors the diagnosis may be only merely ‘possible’, or even unacceptable. Laboratory diagnosis of vWD includes screening tests and confirmatory tests. vWD Types 2 and 3 are relatively easy to diagnose and appear to be genetic disease of a single locus, the vWF gene. As new genetic and possibly non‐genetic factors are discovered, the diagnosis of vWD Type 1 may become easier.</jats:p> |
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| author | BATLLE, J., TOREA, J., RENDAL, E., FERNÁNDEZ, M.F.L. |
| author_facet | BATLLE, J., TOREA, J., RENDAL, E., FERNÁNDEZ, M.F.L., BATLLE, J., TOREA, J., RENDAL, E., FERNÁNDEZ, M.F.L. |
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| description | <jats:p>Diagnosis of von Willebrand's disease (vWD), particularly vWD Type 1. remains a clinical problem for several aspects. Its definitive diagnosis requires documentation of three factors: bleeding, low levels of qualitively normal von Willebrand factor (vWF), and inheritance. In the absence of any of these factors the diagnosis may be only merely ‘possible’, or even unacceptable. Laboratory diagnosis of vWD includes screening tests and confirmatory tests. vWD Types 2 and 3 are relatively easy to diagnose and appear to be genetic disease of a single locus, the vWF gene. As new genetic and possibly non‐genetic factors are discovered, the diagnosis of vWD Type 1 may become easier.</jats:p> |
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| imprint | Wiley, 1997 |
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| physical | 121-128 |
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| series | Journal of Internal Medicine |
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| spelling | BATLLE, J. TOREA, J. RENDAL, E. FERNÁNDEZ, M.F.L. 0954-6820 1365-2796 Wiley Internal Medicine http://dx.doi.org/10.1111/joim.1997.242.s740.121 <jats:p>Diagnosis of von Willebrand's disease (vWD), particularly vWD Type 1. remains a clinical problem for several aspects. Its definitive diagnosis requires documentation of three factors: bleeding, low levels of qualitively normal von Willebrand factor (vWF), and inheritance. In the absence of any of these factors the diagnosis may be only merely ‘possible’, or even unacceptable. Laboratory diagnosis of vWD includes screening tests and confirmatory tests. vWD Types 2 and 3 are relatively easy to diagnose and appear to be genetic disease of a single locus, the vWF gene. As new genetic and possibly non‐genetic factors are discovered, the diagnosis of vWD Type 1 may become easier.</jats:p> The problem of diagnosing von Willebrand's disease Journal of Internal Medicine |
| spellingShingle | BATLLE, J., TOREA, J., RENDAL, E., FERNÁNDEZ, M.F.L., Journal of Internal Medicine, The problem of diagnosing von Willebrand's disease, Internal Medicine |
| title | The problem of diagnosing von Willebrand's disease |
| title_full | The problem of diagnosing von Willebrand's disease |
| title_fullStr | The problem of diagnosing von Willebrand's disease |
| title_full_unstemmed | The problem of diagnosing von Willebrand's disease |
| title_short | The problem of diagnosing von Willebrand's disease |
| title_sort | the problem of diagnosing von willebrand's disease |
| title_unstemmed | The problem of diagnosing von Willebrand's disease |
| topic | Internal Medicine |
| url | http://dx.doi.org/10.1111/joim.1997.242.s740.121 |