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
1987 5
1988 4
1989 8
1990 3
1991 2
1992 4
1993 4
1994 5
1995 9
1996 5
1997 6
1998 6
1999 5
2000 8
2001 10
2002 10
2003 5
2004 3
2005 5
2006 2
2007 1
2008 2
2009 1
2013 1
2014 1
2015 1
2018 1
2019 1
2020 2
2021 2
2022 2
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

122 results

Results by year

Filters applied: . Clear all
Page 1
Familial adult myoclonic epilepsy (FAME).
Uyama E, Fu YH, Ptácek LJ. Uyama E, et al. Adv Neurol. 2005;95:281-8. Adv Neurol. 2005. PMID: 15508931 Review. No abstract available.
[Oculopharyngodistal myopathy].
Uchino M, Uyama E. Uchino M, et al. Among authors: uyama e. Ryoikibetsu Shokogun Shirizu. 2001;(36):457-61. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11596437 Review. Japanese. No abstract available.
Balint's syndrome.
Uyama E, Uchino M, Ando M. Uyama E, et al. Neurology. 1995 Nov;45(11):2118-9. doi: 10.1212/wnl.45.11.2118. Neurology. 1995. PMID: 7501184 No abstract available.
Mitochondrial localization of PABPN1 in oculopharyngeal muscular dystrophy.
Doki T, Yamashita S, Wei FY, Hara K, Yamamoto T, Zhang Z, Zhang X, Tawara N, Hino H, Uyama E, Kurashige T, Maruyama H, Tomizawa K, Ando Y. Doki T, et al. Among authors: uyama e. Lab Invest. 2019 Nov;99(11):1728-1740. doi: 10.1038/s41374-019-0243-8. Epub 2019 Mar 20. Lab Invest. 2019. PMID: 30894671 Free article.
[Scapuloperoneal syndrome].
Uyama E. Uyama E. Ryoikibetsu Shokogun Shirizu. 2001;(36):462-6. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11596438 Review. Japanese. No abstract available.
[Hereditary amyloidosis].
Tashima K, Uyama E, Uchino M, Ando Y. Tashima K, et al. Among authors: uyama e. Ryoikibetsu Shokogun Shirizu. 1998;(19 Pt 2):636-9. Ryoikibetsu Shokogun Shirizu. 1998. PMID: 9645153 Review. Japanese. No abstract available.
Oculopharyngeal muscular dystrophy in Japan.
Uyama E, Nohira O, Tomé FM, Chateau D, Tokunaga M, Ando M, Maki M, Okabe T, Uchino M. Uyama E, et al. Neuromuscul Disord. 1997 Oct;7 Suppl 1:S41-9. doi: 10.1016/s0960-8966(97)00081-3. Neuromuscul Disord. 1997. PMID: 9392015
D409H/D409H genotype in Gaucher-like disease.
Uyama E, Uchino M, Ida H, Eto Y, Owada M. Uyama E, et al. J Med Genet. 1997 Feb;34(2):175. doi: 10.1136/jmg.34.2.175. J Med Genet. 1997. PMID: 9040001 Free PMC article. No abstract available.
122 results