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Page 1
[Dystonia in cerebral palsy; what are the treatment options?].
van de Pol LA, Bonouvrié LA, Vermeulen RJ, de Koning-Tijssen MAJ, van Egmond ME, Willemsen MA, Buizer AI. van de Pol LA, et al. Among authors: de koning tijssen maj. Ned Tijdschr Geneeskd. 2022 Feb 16;166:D5868. Ned Tijdschr Geneeskd. 2022. PMID: 35499589 Review. Dutch.
[Deep brain stimulation for movement disorders].
Beudel M, Oterdoom DLM, van Egmond ME, van Laar T, de Koning-Tijssen MAJ, van Dijk JMC. Beudel M, et al. Among authors: de koning tijssen maj. Ned Tijdschr Geneeskd. 2019 Aug 6;163:D3758. Ned Tijdschr Geneeskd. 2019. PMID: 31386315 Dutch.
['Stiff-person'-syndrome].
Vogels RL, van Orshoven NP, de Koning-Tijssen MA, Wouda EJ. Vogels RL, et al. Ned Tijdschr Geneeskd. 2003 Jun 21;147(25):1228-32. Ned Tijdschr Geneeskd. 2003. PMID: 12848059 Dutch.
[Facial tics and spasms].
Potgieser AR, van Dijk JM, Elting JW, de Koning-Tijssen MA. Potgieser AR, et al. Ned Tijdschr Geneeskd. 2014;158:A7615. Ned Tijdschr Geneeskd. 2014. PMID: 24988167 Review. Dutch.
Worldwide barriers to genetic testing for movement disorders.
Gatto EM, Walker RH, Gonzalez C, Cesarini M, Cossu G, Stephen CD, Balint B, Rodríguez-Violante M, Jankovic J, Morgante F, Jinnah HA; Rare Movement Disorders Study Group of the International Parkinson Disease, Movement Disorders Society. Gatto EM, et al. Eur J Neurol. 2021 Jun;28(6):1901-1909. doi: 10.1111/ene.14826. Epub 2021 Apr 9. Eur J Neurol. 2021. PMID: 33730413
Early onset ataxia with comorbid myoclonus and epilepsy: A disease spectrum with shared molecular pathways and cortico-thalamo-cerebellar network involvement.
van Noort SAM, van der Veen S, de Koning TJ, de Koning-Tijssen MAJ, Verbeek DS, Sival DA. van Noort SAM, et al. Among authors: de koning tijssen maj. Eur J Paediatr Neurol. 2023 Jul;45:47-54. doi: 10.1016/j.ejpn.2023.05.009. Epub 2023 May 23. Eur J Paediatr Neurol. 2023. PMID: 37301083 Free article.