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

Year Number of Results
1993 1
1995 1
1996 2
1997 2
1998 4
1999 4
2000 7
2001 2
2002 3
2003 2
2004 4
2005 4
2006 4
2007 5
2008 6
2009 5
2010 10
2011 9
2012 11
2013 9
2014 8
2015 12
2016 11
2017 13
2018 9
2019 6
2020 5
2021 9
2022 6
2023 6
2024 2

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160 results

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Page 1
Serine Deficiency Disorders.
van der Crabben SN, de Koning TJ. van der Crabben SN, et al. Among authors: de koning tj. 2023 Jun 22. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2023 Jun 22. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 37347880 Free Books & Documents. 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.
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.
Parkinsonism in Genetic Neurodevelopmental Disorders: A Systematic Review.
von Scheibler ENMM, van Eeghen AM, de Koning TJ, Kuijf ML, Zinkstok JR, Müller AR, van Amelsvoort TAMJ, Boot E. von Scheibler ENMM, et al. Among authors: de koning tj. Mov Disord Clin Pract. 2022 Oct 31;10(1):17-31. doi: 10.1002/mdc3.13577. eCollection 2023 Jan. Mov Disord Clin Pract. 2022. PMID: 36699000 Free PMC article. 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.
Developmental neurobiology of cerebellar and Basal Ganglia connections.
Sival DA, Noort SAMV, Tijssen MAJ, de Koning TJ, Verbeek DS. Sival DA, et al. Among authors: de koning tj. Eur J Paediatr Neurol. 2022 Jan;36:123-129. doi: 10.1016/j.ejpn.2021.12.001. Epub 2021 Dec 7. Eur J Paediatr Neurol. 2022. PMID: 34954622 Free article. Review.
Using the shared genetics of dystonia and ataxia to unravel their pathogenesis.
Nibbeling EA, Delnooz CC, de Koning TJ, Sinke RJ, Jinnah HA, Tijssen MA, Verbeek DS. Nibbeling EA, et al. Among authors: de koning tj. Neurosci Biobehav Rev. 2017 Apr;75:22-39. doi: 10.1016/j.neubiorev.2017.01.033. Epub 2017 Jan 28. Neurosci Biobehav Rev. 2017. PMID: 28143763 Free PMC article. Review.
Gut Microbiome Composition in Dystonia Patients.
Timmers ER, Swarte JC, Gacesa R, Björk JR, Weersma RK, Tijssen MAJ, de Koning TJ, Harmsen HJM, Niezen-Koning KE. Timmers ER, et al. Among authors: de koning tj. Int J Mol Sci. 2023 Jan 25;24(3):2383. doi: 10.3390/ijms24032383. Int J Mol Sci. 2023. PMID: 36768705 Free PMC article.
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.
160 results