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

Year Number of Results
1987 3
1988 1
1990 3
1991 1
1993 1
1994 2
1995 1
1996 2
1997 2
1998 4
1999 6
2000 7
2001 2
2002 3
2003 2
2004 6
2005 4
2006 5
2007 6
2008 7
2009 7
2010 12
2011 9
2012 12
2013 9
2014 8
2015 13
2016 12
2017 14
2018 9
2019 10
2020 7
2021 12
2022 1
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183 results
Results by year
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Page 1
A novel diagnostic approach to patients with myoclonus.
Zutt R, van Egmond ME, Elting JW, van Laar PJ, Brouwer OF, Sival DA, Kremer HP, de Koning TJ, Tijssen MA. Zutt R, et al. Among authors: de koning tj. Nat Rev Neurol. 2015 Dec;11(12):687-97. doi: 10.1038/nrneurol.2015.198. Epub 2015 Nov 10. Nat Rev Neurol. 2015. PMID: 26553594 Review.
Treatable inherited rare movement disorders.
Jinnah HA, Albanese A, Bhatia KP, Cardoso F, Da Prat G, de Koning TJ, Espay AJ, Fung V, Garcia-Ruiz PJ, Gershanik O, Jankovic J, Kaji R, Kotschet K, Marras C, Miyasaki JM, Morgante F, Munchau A, Pal PK, Rodriguez Oroz MC, Rodríguez-Violante M, Schöls L, Stamelou M, Tijssen M, Uribe Roca C, de la Cerda A, Gatto EM; International Parkinson's Disease Movement Disorders Society Task Force on Rare Movement Disorders. Jinnah HA, et al. Among authors: de koning tj. Mov Disord. 2018 Jan;33(1):21-35. doi: 10.1002/mds.27140. Epub 2017 Sep 1. Mov Disord. 2018. PMID: 28861905 Free PMC article. Review.
Amino acid synthesis deficiencies.
de Koning TJ. de Koning TJ. J Inherit Metab Dis. 2017 Jul;40(4):609-620. doi: 10.1007/s10545-017-0063-1. Epub 2017 Jun 26. J Inherit Metab Dis. 2017. PMID: 28653176 Free PMC article. Review.
Serine-deficiency syndromes.
de Koning TJ, Klomp LW. de Koning TJ, et al. Curr Opin Neurol. 2004 Apr;17(2):197-204. doi: 10.1097/00019052-200404000-00019. Curr Opin Neurol. 2004. PMID: 15021249 Review.
Amino acid synthesis deficiencies.
de Koning TJ. de Koning TJ. Handb Clin Neurol. 2013;113:1775-83. doi: 10.1016/B978-0-444-59565-2.00047-2. Handb Clin Neurol. 2013. PMID: 23622400 Review.
A clinical diagnostic algorithm for early onset cerebellar ataxia.
Brandsma R, Verschuuren-Bemelmans CC, Amrom D, Barisic N, Baxter P, Bertini E, Blumkin L, Brankovic-Sreckovic V, Brouwer OF, Bürk K, Catsman-Berrevoets CE, Craiu D, de Coo IFM, Gburek J, Kennedy C, de Koning TJ, Kremer HPH, Kumar R, Macaya A, Micalizzi A, Mirabelli-Badenier M, Nemeth A, Nuovo S, Poll-The B, Lerman-Sagie T, Steinlin M, Synofzik M, Tijssen MAJ, Vasco G, Willemsen MAAP, Zanni G, Valente EM, Boltshauser E, Sival DA. Brandsma R, et al. Among authors: de koning tj. Eur J Paediatr Neurol. 2019 Sep;23(5):692-706. doi: 10.1016/j.ejpn.2019.08.004. Epub 2019 Aug 10. Eur J Paediatr Neurol. 2019. PMID: 31481303 Review.
Neurometabolic disorders are treatable causes of dystonia.
Kuiper A, Eggink H, Tijssen MA, de Koning TJ. Kuiper A, et al. Among authors: de koning tj. Rev Neurol (Paris). 2016 Aug-Sep;172(8-9):455-464. doi: 10.1016/j.neurol.2016.07.011. Epub 2016 Aug 22. Rev Neurol (Paris). 2016. PMID: 27561437 Review.
Serotonergic perturbations in dystonia disorders-a systematic review.
Smit M, Bartels AL, van Faassen M, Kuiper A, Niezen-Koning KE, Kema IP, Dierckx RA, de Koning TJ, Tijssen MA. Smit M, et al. Among authors: de koning tj. Neurosci Biobehav Rev. 2016 Jun;65:264-75. doi: 10.1016/j.neubiorev.2016.03.015. Epub 2016 Apr 9. Neurosci Biobehav Rev. 2016. PMID: 27073048 Review.
Musculoskeletal manifestations of lysosomal storage disorders.
Aldenhoven M, Sakkers RJ, Boelens J, de Koning TJ, Wulffraat NM. Aldenhoven M, et al. Among authors: de koning tj. Ann Rheum Dis. 2009 Nov;68(11):1659-65. doi: 10.1136/ard.2008.095315. Ann Rheum Dis. 2009. PMID: 19822711 Review.
D-serine: the right or wrong isoform?
Fuchs SA, Berger R, de Koning TJ. Fuchs SA, et al. Among authors: de koning tj. Brain Res. 2011 Jul 15;1401:104-17. doi: 10.1016/j.brainres.2011.05.039. Epub 2011 May 23. Brain Res. 2011. PMID: 21676380 Review.
183 results