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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: van amelsvoort tamj, van eeghen am. 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.
[Fragile X syndrome: new therapeutic strategies].
Zeidler S, Dierckx B, Lubbers K, van Eeghen AM, Lincke CR, Kievit JA, Willemsen R, Rietman A. Zeidler S, et al. Among authors: van eeghen am. Tijdschr Psychiatr. 2018;60(5):338-342. Tijdschr Psychiatr. 2018. PMID: 29766482 Free article. Review. Dutch.
An aetiological study of 25 mentally retarded adults with autism.
van Karnebeek CD, van Gelderen I, Nijhof GJ, Abeling NG, Vreken P, Redeker EJ, van Eeghen AM, Hoovers JM, Hennekam RC. van Karnebeek CD, et al. Among authors: van gelderen i, van eeghen am. J Med Genet. 2002 Mar;39(3):205-13. doi: 10.1136/jmg.39.3.205. J Med Genet. 2002. PMID: 11897827 Free PMC article. No abstract available.
Methylphenidate for attention-deficit/hyperactivity disorder in patients with Smith-Magenis syndrome: protocol for a series of N-of-1 trials.
Müller AR, Zinkstok JR, Rommelse NNJ, van de Ven PM, Roes KCB, Wijburg FA, de Rooij-Askes E, Linders C, Boot E, van Eeghen AM. Müller AR, et al. Among authors: van eeghen am, van de ven pm. Orphanet J Rare Dis. 2021 Sep 8;16(1):380. doi: 10.1186/s13023-021-02003-z. Orphanet J Rare Dis. 2021. PMID: 34496899 Free PMC article.
48 results