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Fig. 2 | Acta Neuropathologica Communications

Fig. 2

From: Phosphorylated TDP-43 (pTDP-43) aggregates in the axial skeletal muscle of patients with sporadic and familial amyotrophic lateral sclerosis

Fig. 2

N-terminal TDP-43 immunohistochemistry in a control brain (frontotemporal lobar degeneration) and three ALS muscle samples shown to have pTDP-43-reactive inclusions. N-terminal TDP-43 immunohistochemistry reveals cytoplasmic inclusions (black arrows), as demonstrated separately with pTDP-43 immunohistochemistry. There is a loss of normal nuclear staining in affected myofibers. In sample ALS34 (bottom left) a small nerve is present (white arrow), which does not show pathologic staining in the adjacent panel (white arrow). All images are photographed at 400×

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