Agnies M van Eeghen (A M van Eeghen)

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 12

Top Topics

Intellectual Disability

Deep Brain Stimulation

Autism Spectrum Disorder

Top Venues

Therapeutic advances in rare disease

American journal of medical genetics. Part A

Movement disorders clinical practice

Orphanet journal of rare diseases

This page only lists publications with an associated author ORCID identifier.

Publications

Annelieke R Müller, Nadia Y van Silfhout, Bibiche den Hollander, Dick H C Kampman, Lianne Bakkum, Marion M M G Brands, Lotte Haverman, Caroline B Terwee, Carlo Schuengel, Joost Daams, David Hessl, Frits A Wijburg, Erik Boot, Agnies M van Eeghen
Navigating the outcome maze: a scoping review of outcomes and instruments in clinical trials in genetic neurodevelopmental disorders and intellectual disability. Therapeutic advances in rare disease 5 (2024)
Annelieke R Müller, Erik Boot, Stijn B Notermans, Carlo Schuengel, Lidewij Henneman, Martina C Cornel, Mieke M van Haelst, Mariëlle Alders, Clara D M van Karnebeek, Bas Bijl, Frits A Wijburg, Agnies M van Eeghen
Do we care? Reporting of genetic diagnoses in multidisciplinary intellectual disability care: a retrospective chart review. Orphanet journal of rare diseases 19 (1) (2024)
Annelieke R Müller, Nadia Y van Silfhout, Bibiche den Hollander, Dick H C Kampman, Lianne Bakkum, Marion M M G Brands, Lotte Haverman, Caroline B Terwee, Carlo Schuengel, Joost Daams, David Hessl, Frits A Wijburg, Erik Boot, Agnies M van Eeghen
Navigating the outcome maze: a scoping review of outcomes and instruments in clinical trials in genetic neurodevelopmental disorders and intellectual disability. Therapeutic advances in rare disease 5 (2024)
Annelieke R Müller, Nadia Y van Silfhout, Bibiche den Hollander, Dick H C Kampman, Lianne Bakkum, Marion M M G Brands, Lotte Haverman, Caroline B Terwee, Carlo Schuengel, Joost Daams, David Hessl, Frits A Wijburg, Erik Boot, Agnies M van Eeghen
Navigating the outcome maze: a scoping review of outcomes and instruments in clinical trials in genetic neurodevelopmental disorders and intellectual disability. Therapeutic advances in rare disease 5 (2024)
Emma N M M von Scheibler, Josine C C Widdershoven, Denise C P B M van Barneveld, Nina Schröder, Agnies M van Eeghen, Therese A M J van Amelsvoort, Erik Boot
Hearing loss and history of otolaryngological conditions in adults with microdeletion 22q11.2. American journal of medical genetics. Part A (2023)
Petrus J de Vries, Tosca-Marie Heunis, Stephanie Vanclooster, Nola J Chambers, Stacey Bissell, Anna W Byars, Jennifer Flinn, Tanjala T Gipson, Agnies M van Eeghen, Robert Waltereit, Jamie K Capal, Sebastián Cukier, Peter E Davis, Catherine Smith, J Chris Kingswood, Eva Schoeters, Shoba Srivastava, Megumi Takei, Sugnet Gardner-Lubbe, Aubrey J Kumm, Darcy A Krueger, Mustafa Sahin, Liesbeth De Waele, Anna C Jansen
International consensus recommendations for the identification and treatment of tuberous sclerosis complex-associated neuropsychiatric disorders (TAND). Journal of neurodevelopmental disorders 15 (1) (2023)
Agnies M van Eeghen, Hilgo Bruining, Nicole I Wolf, Arthur A Bergen, Riekelt H Houtkooper, Mieke M van Haelst, Clara D van Karnebeek
Personalized medicine for rare neurogenetic disorders: can we make it happen? Cold Spring Harbor molecular case studies 8 (2) (2022)
Emma N M M von Scheibler, Agnies M van Eeghen, Tom J de Koning, Mark L Kuijf, Janneke R Zinkstok, Annelieke R Müller, Therese A M J van Amelsvoort, Erik Boot
Parkinsonism in Genetic Neurodevelopmental Disorders: A Systematic Review. Movement disorders clinical practice 10 (1) (2022)
Emma N M M von Scheibler, Agnies M van Eeghen, Tom J de Koning, Mark L Kuijf, Janneke R Zinkstok, Annelieke R Müller, Therese A M J van Amelsvoort, Erik Boot
Parkinsonism in Genetic Neurodevelopmental Disorders: A Systematic Review. Movement disorders clinical practice 10 (1) (2022)
Emma N M M von Scheibler, Emilie Sophie van der Valk Bouman, Myrthe A Nuijts, Noël J C Bauer, Tos T J M Berendschot, Pit Vermeltfoort, Levinus A Bok, Agnies M van Eeghen, Michiel L Houben, Therese A M J van Amelsvoort, Erik Boot, Michelle B van Egmond-Ebbeling
Ocular findings in 22q11.2 deletion syndrome: A systematic literature review and results of a Dutch multicenter study. American journal of medical genetics. Part A (2021)
A R Müller, J R Zinkstok, N N J Rommelse, P M van de Ven, K C B Roes, F A Wijburg, E de Rooij-Askes, C Linders, E Boot, Agnies M van Eeghen
Methylphenidate for attention-deficit/hyperactivity disorder in patients with Smith-Magenis syndrome: protocol for a series of N-of-1 trials. Orphanet journal of rare diseases 16 (1) (2021)
Annelieke R Müller, Marion M M G Brands, Peter M van de Ven, Kit C B Roes, Martina Cornelia Cornel, Clara D M van Karnebeek, Frits A Wijburg, Joost G Daams, Erik Boot, Agnies M van Eeghen
Systematic Review of N-of-1 Studies in Rare Genetic Neurodevelopmental Disorders: The Power of 1. Neurology 96 (11) (2021)