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

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1984 1
1992 1
1993 3
1994 4
1995 6
1996 3
1997 2
1998 2
1999 4
2000 6
2001 4
2002 3
2003 5
2004 2
2005 5
2006 4
2007 7
2008 9
2009 2
2010 5
2011 4
2012 1
2013 3
2014 3
2015 4
2016 2
2017 3
2018 2
2019 1
2020 1
2021 1
2022 2
2023 1
2024 0

Text availability

Article attribute

Article type

Publication date

Similar articles for PMID: 11593450

101 results

Results by year

Filters applied: . Clear all
Page 1
Huntington disease phenocopy is a familial prion disease.
Moore RC, Xiang F, Monaghan J, Han D, Zhang Z, Edström L, Anvret M, Prusiner SB. Moore RC, et al. Am J Hum Genet. 2001 Dec;69(6):1385-8. doi: 10.1086/324414. Epub 2001 Oct 9. Am J Hum Genet. 2001. PMID: 11593450 Free PMC article.
Exclusion of mutations in the PRNP, JPH3, TBP, ATN1, CREBBP, POU3F2 and FTL genes as a cause of disease in Portuguese patients with a Huntington-like phenotype.
Costa MDC, Teixeira-Castro A, Constante M, Magalhães M, Magalhães P, Cerqueira J, Vale J, Passão V, Barbosa C, Robalo C, Coutinho P, Barros J, Santos MM, Sequeiros J, Maciel P. Costa MDC, et al. J Hum Genet. 2006;51(8):645-651. doi: 10.1007/s10038-006-0001-9. Epub 2006 Jul 21. J Hum Genet. 2006. PMID: 16858508 Free PMC article.
101 results