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

Year Number of Results
1984 1
1987 5
1988 1
1991 1
1992 1
1993 1
1995 1
1996 3
1997 3
1998 4
1999 6
2000 7
2001 2
2002 3
2003 2
2004 6
2005 4
2006 5
2007 5
2008 8
2009 7
2010 12
2011 10
2012 18
2013 9
2014 8
2015 13
2016 13
2017 14
2018 9
2019 7
2020 7
2021 12
2022 7
2023 9
2024 4

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200 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.
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.
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.
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.
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.
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.
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.
200 results