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Results by year

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

Year Number of Results
1995 1
1997 1
1998 2
1999 1
2002 1
2009 1
2015 3
2016 5
2017 3
2018 3
2019 1
2024 0

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Publication date

PubMed (Bookshelf cited) for id: 355137

18 results

Results by year

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Page 1
Clinical Variability in P102L Gerstmann-Sträussler-Scheinker Syndrome.
Tesar A, Matej R, Kukal J, Johanidesova S, Rektorova I, Vyhnalek M, Keller J, Eliasova I, Parobkova E, Smetakova M, Musova Z, Rusina R. Tesar A, et al. Ann Neurol. 2019 Nov;86(5):643-652. doi: 10.1002/ana.25579. Epub 2019 Sep 4. Ann Neurol. 2019. PMID: 31397917
Genetic Creutzfeldt-Jakob disease.
Ladogana A, Kovacs GG. Ladogana A, et al. Handb Clin Neurol. 2018;153:219-242. doi: 10.1016/B978-0-444-63945-5.00013-1. Handb Clin Neurol. 2018. PMID: 29887139
Genetic PrP Prion Diseases.
Kim MO, Takada LT, Wong K, Forner SA, Geschwind MD. Kim MO, et al. Cold Spring Harb Perspect Biol. 2018 May 1;10(5):a033134. doi: 10.1101/cshperspect.a033134. Cold Spring Harb Perspect Biol. 2018. PMID: 28778873 Free PMC article. Review.
Doxycycline in early CJD: a double-blinded randomised phase II and observational study.
Varges D, Manthey H, Heinemann U, Ponto C, Schmitz M, Schulz-Schaeffer WJ, Krasnianski A, Breithaupt M, Fincke F, Kramer K, Friede T, Zerr I. Varges D, et al. J Neurol Neurosurg Psychiatry. 2017 Feb;88(2):119-125. doi: 10.1136/jnnp-2016-313541. Epub 2016 Nov 2. J Neurol Neurosurg Psychiatry. 2017. PMID: 27807198 Free PMC article. Clinical Trial.
Hereditary Human Prion Diseases: an Update.
Schmitz M, Dittmar K, Llorens F, Gelpi E, Ferrer I, Schulz-Schaeffer WJ, Zerr I. Schmitz M, et al. Mol Neurobiol. 2017 Aug;54(6):4138-4149. doi: 10.1007/s12035-016-9918-y. Epub 2016 Jun 20. Mol Neurobiol. 2017. PMID: 27324792 Free article. Review.
Rapidly Progressive Dementia.
Geschwind MD. Geschwind MD. Continuum (Minneap Minn). 2016 Apr;22(2 Dementia):510-37. doi: 10.1212/CON.0000000000000319. Continuum (Minneap Minn). 2016. PMID: 27042906 Free PMC article. Review.
Timing, rates and spectra of human germline mutation.
Rahbari R, Wuster A, Lindsay SJ, Hardwick RJ, Alexandrov LB, Turki SA, Dominiczak A, Morris A, Porteous D, Smith B, Stratton MR; UK10K Consortium; Hurles ME. Rahbari R, et al. Nat Genet. 2016 Feb;48(2):126-133. doi: 10.1038/ng.3469. Epub 2015 Dec 14. Nat Genet. 2016. PMID: 26656846 Free PMC article.
Clinical findings and diagnosis in genetic prion diseases in Germany.
Krasnianski A, Heinemann U, Ponto C, Kortt J, Kallenberg K, Varges D, Schulz-Schaeffer WJ, Kretzschmar HA, Zerr I. Krasnianski A, et al. Eur J Epidemiol. 2016 Feb;31(2):187-96. doi: 10.1007/s10654-015-0049-y. Epub 2015 Jun 16. Eur J Epidemiol. 2016. PMID: 26076917
18 results