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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.
Challenges in Clinicogenetic Correlations: One Phenotype - Many Genes.
Gannamani R, van der Veen S, van Egmond M, de Koning TJ, Tijssen MAJ. Gannamani R, et al. Among authors: de koning tj. Mov Disord Clin Pract. 2021 Mar 2;8(3):311-321. doi: 10.1002/mdc3.13163. eCollection 2021 Apr. Mov Disord Clin Pract. 2021. PMID: 33816658 Free PMC article. Review.
Cortical Myoclonus in a Young Boy with GOSR2 Mutation Mimics Chorea.
van Egmond ME, Kuiper A, Elting JWJ, Brouwer OF, de Koning TJ, Tijssen MAJ. van Egmond ME, et al. Among authors: de koning tj. Mov Disord Clin Pract. 2015 Feb 24;2(1):61-63. doi: 10.1002/mdc3.12136. eCollection 2015 Mar. Mov Disord Clin Pract. 2015. PMID: 30713879 Free PMC article. No abstract available.
The Wide Phenotypic Spectrum of L-2 Hydroxyglutaric Aciduria in Adults.
Mainka T, Ziagaki A, de Koning TJ, Kühn AA, Ganos C. Mainka T, et al. Among authors: de koning tj. Mov Disord Clin Pract. 2020 Sep 30;7(8):1004-1006. doi: 10.1002/mdc3.13092. eCollection 2020 Nov. Mov Disord Clin Pract. 2020. PMID: 33163579 Free PMC article. No abstract available.
Clinical Pearls - how my patients taught me: The fainting lark symptom.
Kuiper A, van Egmond ME, Harms MP, Oosterhoff MD, van Harten B, Sival DA, de Koning TJ, Tijssen MA. Kuiper A, et al. Among authors: de koning tj. J Clin Mov Disord. 2016 Nov 2;3:16. doi: 10.1186/s40734-016-0045-8. eCollection 2016. J Clin Mov Disord. 2016. PMID: 27822381 Free PMC article.
169 results