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
1964 1
1991 1
1992 1
1994 1
1995 1
1996 1
1997 2
1998 4
1999 8
2000 5
2001 5
2002 3
2003 13
2004 6
2005 6
2006 7
2007 10
2008 3
2009 5
2010 9
2011 5
2012 6
2013 9
2014 5
2015 10
2016 7
2017 11
2018 8
2019 6
2020 13
2021 10
2022 3
2023 8
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

174 results

Results by year

Filters applied: . Clear all
Page 1
Editorial: Prodromal Parkinson's Disease.
Crosiers D, Santens P, Chaudhuri KR. Crosiers D, et al. Among authors: santens p. Front Neurol. 2021 Jan 12;11:634490. doi: 10.3389/fneur.2020.634490. eCollection 2020. Front Neurol. 2021. PMID: 33584526 Free PMC article. No abstract available.
Central auditory processing in parkinsonian disorders: A systematic review.
De Groote E, De Keyser K, Bockstael A, Botteldooren D, Santens P, De Letter M. De Groote E, et al. Among authors: santens p. Neurosci Biobehav Rev. 2020 Jun;113:111-132. doi: 10.1016/j.neubiorev.2020.03.001. Epub 2020 Mar 4. Neurosci Biobehav Rev. 2020. PMID: 32145223 Review.
Exome Sequencing and Multigene Panel Testing in 1,411 Patients With Adult-Onset Neurologic Disorders.
Schuermans N, Verdin H, Ghijsels J, Hellemans M, Debackere E, Bogaert E, Symoens S, Naesens L, Lecomte E, Crosiers D, Bergmans B, Verhoeven K, Poppe B, Laureys G, Herdewyn S, Van Langenhove T, Santens P, De Bleecker JL, Hemelsoet D, Dermaut B; for Program for Undiagnosed Rare Diseases (UD-PrOZA). Schuermans N, et al. Among authors: santens p. Neurol Genet. 2023 Apr 26;9(3):e200071. doi: 10.1212/NXG.0000000000200071. eCollection 2023 Jun. Neurol Genet. 2023. PMID: 37152446 Free PMC article.
Extended FTLD pedigree segregating a Belgian GRN-null mutation: neuropathological heterogeneity in one family.
Sieben A, Van Mossevelde S, Wauters E, Engelborghs S, van der Zee J, Van Langenhove T, Santens P, Praet M, Boon P, Miatton M, Van Hoecke S, Vandenbulcke M, Vandenberghe R, Cras P, Cruts M, De Deyn PP, Van Broeckhoven C, Martin JJ. Sieben A, et al. Among authors: santens p. Alzheimers Res Ther. 2018 Jan 22;10(1):7. doi: 10.1186/s13195-017-0334-y. Alzheimers Res Ther. 2018. PMID: 29370838 Free PMC article. Review.
174 results