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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
Schizophrenia as a prodromal symptom in a patient harboring SNCA duplication.
Takamura S, Ikeda A, Nishioka K, Furuya H, Tashiro M, Matsushima T, Li Y, Yoshino H, Funayama M, Morinobu S, Hattori N. Takamura S, et al. Among authors: ikeda a. Parkinsonism Relat Disord. 2016 Apr;25:108-9. doi: 10.1016/j.parkreldis.2016.01.028. Epub 2016 Feb 8. Parkinsonism Relat Disord. 2016. PMID: 26880146
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.
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.
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
Clinical characterization of patients with leucine-rich repeat kinase 2 genetic variants in Japan.
Li Y, Ikeda A, Yoshino H, Oyama G, Kitani M, Daida K, Hayashida A, Ogaki K, Yoshida K, Kimura T, Nakayama Y, Ito H, Sugeno N, Aoki M, Miyajima H, Kimura K, Ueda N, Watanabe M, Urabe T, Takanashi M, Funayama M, Nishioka K, Hattori N. Li Y, et al. Among authors: ikeda a. J Hum Genet. 2020 Sep;65(9):771-781. doi: 10.1038/s10038-020-0772-4. Epub 2020 May 13. J Hum Genet. 2020. PMID: 32398759
Homeostatic p62 levels and inclusion body formation in CHCHD2 knockout mice.
Sato S, Noda S, Torii S, Amo T, Ikeda A, Funayama M, Yamaguchi J, Fukuda T, Kondo H, Tada N, Arakawa S, Watanabe M, Uchiyama Y, Shimizu S, Hattori N. Sato S, et al. Among authors: ikeda a. Hum Mol Genet. 2021 Apr 30;30(6):443-453. doi: 10.1093/hmg/ddab057. Hum Mol Genet. 2021. PMID: 33631794
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
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.
1,914 results