Notes
Keine oder weniger als 4 Marklagerläsionen bzw. weniger als 3 Marklagerläsionen, wenn hiervon eine periventrikulär liegt.
Wurde zu Erkrankungsbeginn kein kraniales MRT angefertigt oder ist der Befund unbekannt, sollte das früheste verfügbare MRT herangezogen werden [85].
Der Nachweis von NMO-IgG mittels Immunhistochemie [43] kann durch den Nachweis von AQP4-Ak mittels rekombinanter Verfahren ersetzt werden. Voraussetzung ist, dass das gewählte rekombinante Testverfahren anhand eines NMO-IgG-positiven Kollektivs erfolgreich validiert wurde. Unter den bislang (Stand: Oktober 2010) in der wissenschaftlichen Literatur beschriebenen und gegenwärtig für diagnostische Zwecke zur Verfügung stehenden Testsystemen erfüllen lediglich die sog. zellbasierten Assays diese Voraussetzung [29, 35, 79].
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Interessenkonflikt
Die korrespondierende Autorin weist auf folgende Beziehungen hin:
C. Trebst hat Honorare für wissenschaftliche Vorträge und Reiseunterstützung erhalten von Bayer Health Care, Biogen Idec, Diamed Medizintechnik, Merck Serono, Sanofi Aventis und Talecris Biotherapeutics.
A. Berthele, S. Schippling, B. Wildemann und C. Wilke haben keine Interessenskonflikte.
S. Jarius erhält Forschungsunterstützung von Bayer Schering und Merck Serono und hat ein Fellowship des European Committee for Treatment and Research in Multiple Sclerosis (ECTRIMS) erhalten.
T. Kümpfel hat Honorare für wissenschaftliche Vorträge und Reiseunterstützung erhalten von Bayer Schering, Teva/Sanofi- Aventis, Merck-Serono and Biogen-Idec sowie Forschungsunterstützung von Bayer Schering.
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Trebst, C., Berthele, A., Jarius, S. et al. Diagnostik und Therapie der Neuromyelitis optica. Nervenarzt 82, 768–777 (2011). https://doi.org/10.1007/s00115-010-3192-4
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DOI: https://doi.org/10.1007/s00115-010-3192-4