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- W2790825942 abstract "Schwannomatosis and neurofibromatosis type 2 are hereditary tumor syndromes, and peripheral neuropathy has been reported in both. We prospectively applied in vivo morphometric measurement of dorsal root ganglia volume in 16 schwannomatosis patients, 14 neurofibromatosis type 2 patients, and 26 healthy controls by magnetic resonance neurography. Compared to healthy controls, dorsal root ganglia hypertrophy was a consistent finding in neurofibromatosis type 2 (L3, + 267%; L4, + 235%; L5, + 241%; S1, + 300%; S2, + 242%; Bonferroni‐adjusted p < 0.001) but not in schwannomatosis. Dorsal root ganglia may be a vulnerable site in origination of areflexia and sensory loss and a useful diagnostic marker in neurofibromatosis type 2. Ann Neurol 2018;83:854–857" @default.
- W2790825942 created "2018-03-29" @default.
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- W2790825942 date "2018-03-25" @default.
- W2790825942 modified "2023-10-14" @default.
- W2790825942 title "Dorsal root ganglia volume differentiates schwannomatosis and neurofibromatosis 2" @default.
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- W2790825942 doi "https://doi.org/10.1002/ana.25191" @default.
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