Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

1,922 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
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
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
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.
GCH1 mutations in dopa-responsive dystonia and Parkinson's disease.
Yoshino H, Nishioka K, Li Y, Oji Y, Oyama G, Hatano T, Machida Y, Shimo Y, Hayashida A, Ikeda A, Mogushi K, Shibagaki Y, Hosaka A, Iwanaga H, Fujitake J, Ohi T, Miyazaki D, Sekijima Y, Oki M, Kusaka H, Fujimoto KI, Ugawa Y, Funayama M, Hattori N. Yoshino H, et al. Among authors: ikeda a. J Neurol. 2018 Aug;265(8):1860-1870. doi: 10.1007/s00415-018-8930-8. Epub 2018 Jun 14. J Neurol. 2018. PMID: 29948246
The identified clinical features of Parkinson's disease in homo-, heterozygous and digenic variants of PINK1.
Hayashida A, Li Y, Yoshino H, Daida K, Ikeda A, Ogaki K, Fuse A, Mori A, Takanashi M, Nakahara T, Yoritaka A, Tomizawa Y, Furukawa Y, Kanai K, Nakayama Y, Ito H, Ogino M, Hattori Y, Hattori T, Ichinose Y, Takiyama Y, Saito T, Kimura T, Aizawa H, Shoji H, Mizuno Y, Matsushita T, Sato M, Sekijima Y, Morita M, Iwasaki A, Kusaka H, Tada M, Tanaka F, Sakiyama Y, Fujimoto T, Nagara Y, Kashihara K, Todo H, Nakao K, Tsuruta K, Yoshikawa M, Hara H, Yokote H, Murase N, Nakamagoe K, Tamaoka A, Takamiya M, Morimoto N, Nokura K, Kako T, Funayama M, Nishioka K, Hattori N. Hayashida A, et al. Among authors: ikeda a. Neurobiol Aging. 2021 Jan;97:146.e1-146.e13. doi: 10.1016/j.neurobiolaging.2020.06.017. Epub 2020 Jul 2. Neurobiol Aging. 2021. PMID: 32713623
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
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
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
Clinical heterogeneity of frontotemporal dementia and Parkinsonism linked to chromosome 17 caused by MAPT N279K mutation in relation to tau positron emission tomography features.
Ikeda A, Shimada H, Nishioka K, Takanashi M, Hayashida A, Li Y, Yoshino H, Funayama M, Ueno Y, Hatano T, Sahara N, Suhara T, Higuchi M, Hattori N. Ikeda A, et al. Mov Disord. 2019 Apr;34(4):568-574. doi: 10.1002/mds.27623. Epub 2019 Feb 17. Mov Disord. 2019. PMID: 30773680 Free PMC article.
1,922 results