Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1991 | 1 |
1995 | 1 |
1999 | 1 |
2024 | 0 |
Search Results
3 results
Results by year
Filters applied: . Clear all
Page 1
Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP gene.
Proc Natl Acad Sci U S A. 1991 Dec 1;88(23):10926-30. doi: 10.1073/pnas.88.23.10926.
Proc Natl Acad Sci U S A. 1991.
PMID: 1683708
Free PMC article.
Prominent psychiatric features and early onset in an inherited prion disease with a new insertional mutation in the prion protein gene.
Laplanche JL, Hachimi KH, Durieux I, Thuillet P, Defebvre L, Delasnerie-Lauprêtre N, Peoc'h K, Foncin JF, Destée A.
Laplanche JL, et al.
Brain. 1999 Dec;122 ( Pt 12):2375-86. doi: 10.1093/brain/122.12.2375.
Brain. 1999.
PMID: 10581230
Item in Clipboard
Hypokinesia and presenile dementia in a Dutch family with a novel insertion in the prion protein gene.
van Gool WA, Hensels GW, Hoogerwaard EM, Wiezer JH, Wesseling P, Bolhuis PA.
van Gool WA, et al.
Brain. 1995 Dec;118 ( Pt 6):1565-71. doi: 10.1093/brain/118.6.1565.
Brain. 1995.
PMID: 8595485
Item in Clipboard
Cite
Cite