Parents

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Jaap Valk grad student 1991 Utrecht
 (Myelination and myelin disorders)
Jacobus Willemse grad student 1991 Utrecht

Children

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Ilja Boor grad student 2008 VU Amsterdam
Mohit Dubey grad student 2011-2015 VUMC
BETA: Related publications

Publications

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Vanderver A, Bernard G, Helman G, et al. (2020) Randomized Clinical Trial of First-Line Genome Sequencing in Pediatric White Matter Disorders. Annals of Neurology
Vanderver A, Bernard G, Helman G, et al. (2020) Randomized Clinical Trial of First-Line Genome Sequencing in Pediatric White Matter Disorders. Annals of Neurology
Wolf NI, van der Knaap MS. (2020) Reader response: Teaching NeuroImages: A rare case of Jacobsen syndrome with global diffuse hypomyelination of brain. Neurology. 94: 458
Wolf NI, Breur M, Plug B, et al. (2020) Metachromatic leukodystrophy and transplantation: remyelination, no cross-correction. Annals of Clinical and Translational Neurology
Wolf NI, Breur M, Plug B, et al. (2020) Metachromatic leukodystrophy and transplantation: remyelination, no cross-correction. Annals of Clinical and Translational Neurology
Helman G, Lajoie BR, Crawford J, et al. (2020) Genome sequencing in persistently unsolved white matter disorders. Annals of Clinical and Translational Neurology
Helman G, Lajoie BR, Crawford J, et al. (2020) Genome sequencing in persistently unsolved white matter disorders. Annals of Clinical and Translational Neurology
Helman G, Lajoie BR, Crawford J, et al. (2020) Genome sequencing in persistently unsolved white matter disorders. Annals of Clinical and Translational Neurology
Mendes MI, Green LMC, Bertini E, et al. (2019) RARS1-related hypomyelinating leukodystrophy: Expanding the spectrum. Annals of Clinical and Translational Neurology
Mendes MI, Green LMC, Bertini E, et al. (2019) RARS1-related hypomyelinating leukodystrophy: Expanding the spectrum. Annals of Clinical and Translational Neurology
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