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Page 1
Prevalence of Parkinson's Disease in 22q11.2 Deletion Syndrome: A Multicenter Study.
von Scheibler ENMM, Swillen A, Repetto GM, Reyes NGD, Lang AE, Marras C, Kuijf ML, Rouhl RPW, van Eeghen AM, Juri C, Vogels A, van Amelsvoort TAMJ, Bassett AS, Boot E. von Scheibler ENMM, et al. Mov Disord Clin Pract. 2025 Jun;12(6):817-822. doi: 10.1002/mdc3.14354. Epub 2025 Feb 7. Mov Disord Clin Pract. 2025. PMID: 39918054 Free PMC article.
Obesity and metabolic syndrome in adults with a 22q11.2 microdeletion.
Jaspers Faijer-Westerink H, von Scheibler ENMM, van Rossum EFC, van Haelst MM, Vingerhoets C, van Amelsvoort TAMJ, van Eeghen AM, Boot E. Jaspers Faijer-Westerink H, et al. Among authors: von scheibler enmm. Int J Obes (Lond). 2025 Apr;49(4):642-648. doi: 10.1038/s41366-024-01685-2. Epub 2024 Nov 30. Int J Obes (Lond). 2025. PMID: 39616274 Free PMC article.
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. 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.
Ocular findings in 22q11.2 deletion syndrome: A systematic literature review and results of a Dutch multicenter study.
von Scheibler ENMM, van der Valk Bouman ES, Nuijts MA, Bauer NJC, Berendschot TTJM, Vermeltfoort P, Bok LA, van Eeghen AM, Houben ML, van Amelsvoort TAMJ, Boot E, van Egmond-Ebbeling MB. von Scheibler ENMM, et al. Am J Med Genet A. 2022 Feb;188(2):569-578. doi: 10.1002/ajmg.a.62556. Epub 2021 Nov 12. Am J Med Genet A. 2022. PMID: 34773366 Free PMC article.