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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 6
2021 11
2022 6
2023 7
2024 6
2025 0

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166 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, 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, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 37347880 Free Books & Documents. Review.
The natural history of progressive myoclonus ataxia.
van der Veen S, Eggink H, Elting JWJ, Sival D, Verschuuren-Bemelmans CC, de Koning TJ, Tijssen MAJ. van der Veen S, et al. Among authors: de koning tj. Neurobiol Dis. 2024 Sep;199:106555. doi: 10.1016/j.nbd.2024.106555. Epub 2024 Jun 4. Neurobiol Dis. 2024. PMID: 38844245 Free article.
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. Handb Clin Neurol. 2013;113:1775-83. doi: 10.1016/B978-0-444-59565-2.00047-2. Handb Clin Neurol. 2013. PMID: 23622400 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.
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.
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.
166 results