Barely Significant
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Naming and conceptual understanding in frontotemporal dementia.

Cortex · 2019 · PMC6838679 · PMID 31220614

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hedged sentence
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closest p · 0.1× alpha
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The sentences

showed a trendp = .007actually significant
Patients with MAPT mutations showed a trend towards more severe atrophy in left entorhinal cortex (U = 2.0, z = −2.68, p = .007) and fusiform gyrus (U = 1.5, z = −2.72, p = .006) and right perirhinal cortex (U = 1.5, z = −2.67, p = .007) than patients with mutations in the GRN and C9orf72 gene and in right fusiform gyrus compared to bvFTD patients with no gene mutation (U = 13.0, z = −2.80, p = .005). 4 Discussion In this large cohort of bvFTD patients naming problems were a prominent feature of many, although not all, patients (around 50%).

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