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Journal of Neurology, Neurosurgery, and Psychiatry|September 11, 2017
Quantitative MR spectroscopic imaging in metachromatic leukodystrophy: value for prognosis and treatmentDiane F van Rappard, Antoine Klauser, Marjan E Steenweg, et al.Iscience|May 31, 2022
AURKA and PLK1 inhibition selectively and synergistically block cell cycle progression in diffuse midline gliomaDennis S Metselaar, Aimée du Chatinier, Michaël H Meel, et al.Journal of Child Neurology|September 29, 2020
Cerebral Microangiopathy in Leukoencephalopathy With Cerebral Calcifications and Cysts: A Pathological DescriptionGuy Helman, Angela N Viaene, Asako Takanohashi, et al.Molecular Neurobiology|July 14, 2023
Understanding the Ultra-Rare Disease Autosomal Dominant Leukodystrophy: an Updated Review on Morpho-Functional Alterations Found in Experimental ModelsIrene Neri, Giulia Ramazzotti, Sara Mongiorgi, et al.Neurobiology of Aging|May 19, 2024
Region-specific and age-related differences in astrocytes in the human brainJodie H K Man, Marjolein Breur, Charlotte A G H van Gelder, et al.Acta Neuropathologica|November 13, 2012
APP mutations in the Aβ coding region are associated with abundant cerebral deposition of Aβ38Maria Luisa Moro, Giorgio Giaccone, Raffaella Lombardi, et al.Journal of Neurology|April 2, 2024
Progressive demyelinating polyneuropathy after hematopoietic cell transplantation in metachromatic leukodystrophy: a case seriesShanice Beerepoot, Jaap Jan Boelens, Caroline Lindemans, et al.The Journal of Biological Chemistry|September 13, 2003
Structural properties of Gerstmann-Straussler-Scheinker disease amyloid proteinMario Salmona, Michela Morbin, Tania Massignan, et al.Archives of Neurology|February 8, 2012
Restricted diffusion in vanishing white matterHannemieke D W van der Lei, Marjan E Steenweg, Marianna Bugiani, et al.Annals of Neurology|April 11, 2017
A mutation in the Tubb4a gene leads to microtubule accumulation with hypomyelination and demyelinationIan D Duncan, Marianna Bugiani, Abigail B Radcliff, et al.Pageof 18