Jeroen Dudink

Human USP18 deficiency underlies type 1 interferonopathy leading to severe pseudo-TORCH syndrome

Marije Meuwissen, Rachel Schot, Sofija Buta et al. · The Journal of Experimental Medicine · 2016 · 278 citations · Full text

Disease Etiology, Genetics, Pseudo-torch Syndrome +17

Mutation in the AP4M1 Gene Provides a Model for Neuroaxonal Injury in Cerebral Palsy

Annemieke J.M.H. Verkerk, Rachel Schot, Belinda Dumee et al. · The American Journal of Human Genetics · 2009 · 172 citations · Full text

Neurodegenerative Diseases, Molecular Neuroscience, Neurological Disorder +13

Feasibility and safety of intranasally administered mesenchymal stromal cells after perinatal arterial ischaemic stroke in the Netherlands (PASSIoN): a first-in-human, open-label intervention study

Lisanne M. Baak, Nienke Wagenaar, Niek E. van der Aa et al. · The Lancet Neurology · 2022 · 151 citations · Full text

Thrombosis, Ischemic Stroke, Medicine +13

COL4A2 mutation associated with familial porencephaly and small-vessel disease

Elly Verbeek, Marije Meuwissen, Frans W. Verheijen et al. · European Journal of Human Genetics · 2012 · 120 citations · Full text

Col4a2 Mutation, Developmental Anomaly, Mendelian Disorder +5

Randomized Controlled Early versus Late Ventricular Intervention Study in Posthemorrhagic Ventricular Dilatation: Outcome at 2 Years

Mehmet Nevzat Çizmeci, Floris Groenendaal, Kian D. Liem et al. · The Journal of Pediatrics · 2020 · 104 citations · Full text

Heart Failure, Cardiovascular Disease, Posthemorrhagic Ventricular Dilatation +7