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Neuroanatomical anomalies due to a defect in the FGF3 gene, associated with the Labyrinthine Aplasia, Microtia and Microdontia syndrome: insights from the placement of auditory brainstem implants in two siblings2024 Therapeutic Advances in Rare Disease article Neuroscience Hearing Loss and Rehabilitation Open access
Johan H. M. Frijns, M. G. S. Geerders, Esther Scholing, Berit M. Verbist, Radboud W. Koot, Martijn J. A. Malessy, +2 more
1citations -
The systemic inhibition of the terminal complement system reduces neuroinflammation but does not improve motor function in mouse models of CMT1A with overexpressed PMP222023 Current Research in Neurobiology article Neuroscience Hereditary Neurological Disorders Open access
Iliana Michailidou, Jeroen P. Vreijling, Matthijs Rumpf, Maarten Loos, Bastijn Koopmans, Nina Vlek, +6 more
8citations
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