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

Year Number of Results
1964 1
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1994 1
1995 1
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1998 4
1999 8
2000 5
2001 5
2002 3
2003 13
2004 6
2005 6
2006 7
2007 10
2008 3
2009 6
2010 9
2011 5
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2014 6
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190 results

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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.
Neuroplasticity in Parkinson's disease.
Popescu BO, Batzu L, Ruiz PJG, Tulbă D, Moro E, Santens P. Popescu BO, et al. Among authors: santens p. J Neural Transm (Vienna). 2024 Nov;131(11):1329-1339. doi: 10.1007/s00702-024-02813-y. Epub 2024 Aug 5. J Neural Transm (Vienna). 2024. PMID: 39102007 Free PMC article. Review.
Safety and efficacy of faecal microbiota transplantation in patients with mild to moderate Parkinson's disease (GUT-PARFECT): a double-blind, placebo-controlled, randomised, phase 2 trial.
Bruggeman A, Vandendriessche C, Hamerlinck H, De Looze D, Tate DJ, Vuylsteke M, De Commer L, Devolder L, Raes J, Verhasselt B, Laukens D, Vandenbroucke RE, Santens P. Bruggeman A, et al. Among authors: santens p. EClinicalMedicine. 2024 Mar 27;71:102563. doi: 10.1016/j.eclinm.2024.102563. eCollection 2024 May. EClinicalMedicine. 2024. PMID: 38686220 Free PMC article.
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.
190 results