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Prominent sensory involvement in a case of familial amyotrophic lateral sclerosis carrying the L8V SOD1 mutation.
Nishiyama A, Warita H, Takahashi T, Suzuki N, Nishiyama S, Tano O, Akiyama T, Watanabe Y, Takahashi K, Kuroda H, Kato M, Tateyama M, Niihori T, Aoki Y, Aoki M. Nishiyama A, et al. Among authors: takahashi k, takahashi t. Clin Neurol Neurosurg. 2016 Nov;150:194-196. doi: 10.1016/j.clineuro.2016.08.008. Epub 2016 Aug 6. Clin Neurol Neurosurg. 2016. PMID: 27543311 No abstract available.
Distribution of TRPVs, P2X3, and parvalbumin in the human nodose ganglion.
Sato D, Sato T, Urata Y, Okajima T, Kawamura S, Kurita M, Takahashi K, Nanno M, Watahiki A, Kokubun S, Shimizu Y, Kasahara E, Shoji N, Sasano T, Ichikawa H. Sato D, et al. Among authors: takahashi k. Cell Mol Neurobiol. 2014 Aug;34(6):851-8. doi: 10.1007/s10571-014-0062-9. Epub 2014 Apr 24. Cell Mol Neurobiol. 2014. PMID: 24764033
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