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

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2012 1
2014 1
2015 1
2016 1
2017 2
2018 2
2019 2
2020 1
2021 3
2022 2
2023 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

15 results

Results by year

Filters applied: . Clear all
Page 1
Essential Tremor with Aspartic Acidemia.
Miura S, Fujioka R, Taniwaki T. Miura S, et al. Among authors: fujioka r. Kurume Med J. 2017 May 8;63(3.4):81-84. doi: 10.2739/kurumemedj.MS00015. Epub 2017 Mar 15. Kurume Med J. 2017. PMID: 28302933 Free article. Review.
A Japanese family with dystonia due to a pathogenic variant in SGCE.
Morikawa T, Miura S, Fan L, Watanabe E, Fujioka R, Motooka H, Yasumoto S, Uchiyama Y, Shibata H. Morikawa T, et al. Among authors: fujioka r. Hum Genome Var. 2022 Aug 22;9(1):29. doi: 10.1038/s41439-022-00207-8. Hum Genome Var. 2022. PMID: 35995778 Free PMC article.
Plasma amino acids in patients with essential tremor.
Miura S, Kamada T, Fujioka R, Yamanishi Y. Miura S, et al. Among authors: fujioka r. Clin Case Rep. 2021 Aug 16;9(8):e04580. doi: 10.1002/ccr3.4580. eCollection 2021 Aug. Clin Case Rep. 2021. PMID: 34429988 Free PMC article.
A novel missense mutation of RYR1 in familial idiopathic hyper CK-emia.
Sano K, Miura S, Fujiwara T, Fujioka R, Yorita A, Noda K, Kida H, Azuma K, Kaieda S, Yamamoto K, Taniwaki T, Fukumaki Y, Shibata H. Sano K, et al. Among authors: fujioka r. J Neurol Sci. 2015 Sep 15;356(1-2):142-7. doi: 10.1016/j.jns.2015.06.035. Epub 2015 Jun 19. J Neurol Sci. 2015. PMID: 26119398
Spinocerebellar ataxia 27 with a novel nonsense variant (Lys177X) in FGF14.
Miura S, Kosaka K, Fujioka R, Uchiyama Y, Shimojo T, Morikawa T, Irie A, Taniwaki T, Shibata H. Miura S, et al. Among authors: fujioka r. Eur J Med Genet. 2019 Mar;62(3):172-176. doi: 10.1016/j.ejmg.2018.07.005. Epub 2018 Jul 11. Eur J Med Genet. 2019. PMID: 30017992
15 results