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In vivo confocal microscopy may show hyperreflective filaments, corresponding to filamentous fungi including Alternaria, and thus may help to establish an early diagnosis [9]; however, this technique is not widely available.
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He may show interest.
From this we show that CARS microscopy may be use as a reliable, non-destructive, in vivo technique with sufficient accuracy to assess axonal myelination of normal and injured peripheral nerves.
Some innovative microscopy may resolve the issue.
Electron microscopy may also be employed for similar studies.
Electron microscopy may help to resolve this question.
Although in PICG, by definition, there is a paucity of immune deposits on immunofluorescence microscopy and electron microscopy, a significant proportion of cases may indeed show Ig deposits on histopathological examination [ 7, 16, 17].
Notably, the microscopy images show a virtually digital behavior.
Our scanning confocal microscopy data show differential localization of hornerin.
Microscopy experiments show colocalization of both fluorescein and MG fluorescence.
Confocal microscopy analysis showed that TIAF1 aggregates may or may not colocalize with A β. TIAF1 aggregates are normally >100 μm in diameter.
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