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Page 1
Clinical characteristics and pathophysiological properties of newly discovered LRRK2 variants associated with Parkinson's disease.
Tezuka T, Ishiguro M, Taniguchi D, Osogaguchi E, Shiba-Fukushima K, Ogata J, Ishii R, Ikeda A, Li Y, Yoshino H, Matsui T, Kaida K, Funayama M, Nishioka K, Kumazawa F, Matsubara T, Tsuda H, Saito Y, Murayama S, Imai Y, Hattori N. Tezuka T, et al. Among authors: ikeda a. Neurobiol Dis. 2024 Sep;199:106571. doi: 10.1016/j.nbd.2024.106571. Epub 2024 Jun 18. Neurobiol Dis. 2024. PMID: 38901781 Free article.
Pathophysiological evaluation of the LRRK2 G2385R risk variant for Parkinson's disease.
Tezuka T, Taniguchi D, Sano M, Shimada T, Oji Y, Tsunemi T, Ikeda A, Li Y, Yoshino H, Ogata J, Shiba-Fukushima K, Funayama M, Nishioka K, Imai Y, Hattori N. Tezuka T, et al. Among authors: ikeda a. NPJ Parkinsons Dis. 2022 Aug 5;8(1):97. doi: 10.1038/s41531-022-00367-y. NPJ Parkinsons Dis. 2022. PMID: 35931783 Free PMC article.
FBXO7 mutations in Parkinson's disease and multiple system atrophy.
Conedera S, Apaydin H, Li Y, Yoshino H, Ikeda A, Matsushima T, Funayama M, Nishioka K, Hattori N. Conedera S, et al. Among authors: ikeda a. Neurobiol Aging. 2016 Apr;40:192.e1-192.e5. doi: 10.1016/j.neurobiolaging.2016.01.003. Epub 2016 Jan 14. Neurobiol Aging. 2016. PMID: 26882974 Review.
Homozygous alpha-synuclein p.A53V in familial Parkinson's disease.
Yoshino H, Hirano M, Stoessl AJ, Imamichi Y, Ikeda A, Li Y, Funayama M, Yamada I, Nakamura Y, Sossi V, Farrer MJ, Nishioka K, Hattori N. Yoshino H, et al. Among authors: ikeda a. Neurobiol Aging. 2017 Sep;57:248.e7-248.e12. doi: 10.1016/j.neurobiolaging.2017.05.022. Epub 2017 Jun 27. Neurobiol Aging. 2017. PMID: 28666710
COQ2 variants in Parkinson's disease and multiple system atrophy.
Mikasa M, Kanai K, Li Y, Yoshino H, Mogushi K, Hayashida A, Ikeda A, Kawajiri S, Okuma Y, Kashihara K, Sato T, Kondo H, Funayama M, Nishioka K, Hattori N. Mikasa M, et al. Among authors: ikeda a. J Neural Transm (Vienna). 2018 Jun;125(6):937-944. doi: 10.1007/s00702-018-1885-1. Epub 2018 Apr 11. J Neural Transm (Vienna). 2018. PMID: 29644397
Genetic analysis of ATP10B for Parkinson's disease in Japan.
Ishiguro M, Yoshino H, Li Y, Ikeda A, Funayama M, Nishioka K, Hattori N. Ishiguro M, et al. Among authors: ikeda a. Parkinsonism Relat Disord. 2021 Jul;88:10-12. doi: 10.1016/j.parkreldis.2021.05.020. Epub 2021 May 29. Parkinsonism Relat Disord. 2021. PMID: 34091411
Genotype-phenotype correlations of cysteine replacement in CADASIL.
Matsushima T, Conedera S, Tanaka R, Li Y, Yoshino H, Funayama M, Ikeda A, Hosaka Y, Okuzumi A, Shimada Y, Yamashiro K, Motoi Y, Nishioka K, Hattori N. Matsushima T, et al. Among authors: ikeda a. Neurobiol Aging. 2017 Feb;50:169.e7-169.e14. doi: 10.1016/j.neurobiolaging.2016.10.026. Epub 2016 Nov 2. Neurobiol Aging. 2017. PMID: 27890607
A novel mutation of CHCHD2 p.R8H in a sporadic case of Parkinson's disease.
Ikeda A, Matsushima T, Daida K, Nakajima S, Conedera S, Li Y, Yoshino H, Oyama G, Funayama M, Nishioka K, Hattori N. Ikeda A, et al. Parkinsonism Relat Disord. 2017 Jan;34:66-68. doi: 10.1016/j.parkreldis.2016.10.018. Epub 2016 Oct 24. Parkinsonism Relat Disord. 2017. PMID: 28341223 No abstract available.
Mutations in CHCHD2 cause α-synuclein aggregation.
Ikeda A, Nishioka K, Meng H, Takanashi M, Hasegawa I, Inoshita T, Shiba-Fukushima K, Li Y, Yoshino H, Mori A, Okuzumi A, Yamaguchi A, Nonaka R, Izawa N, Ishikawa KI, Saiki H, Morita M, Hasegawa M, Hasegawa K, Elahi M, Funayama M, Okano H, Akamatsu W, Imai Y, Hattori N. Ikeda A, et al. Hum Mol Genet. 2019 Dec 1;28(23):3895-3911. doi: 10.1093/hmg/ddz241. Hum Mol Genet. 2019. PMID: 31600778
1,988 results